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Articles de revues sur le sujet « Acetamide »

Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 26 juillet 2025

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1

Nagarsha, K. M., T. M. Sharanakumar, D. Ramesh, et al. "NOVEL SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL ACTIVITY OF N-(5BROMO-2-(5-PHENYL1,3,4-OXADIAZOL-2-YL)NAPHTHA[2,1-B]FURAN-1- YL)ACETAMIDE AND N-(5-NITRO-2-(5-PHENYL-1,3,4- OXADIAZOL-2-YL)NAPHTHA[2,1-BFURAN-1-YL]ACETAMIDE AND THEIR DERIVATIVES." RASAYAN Journal of Chemistry 16, no. 01 (2023): 167–75. http://dx.doi.org/10.31788/rjc.2023.1618088.

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The novel derivatives of naphtho-furan such N-(5bromo-2-(5-phenyl-1,3,4-oxadiazol-2-yl)naphtha[2,1-b]furan-1- yl)acetamide (8), N-(5-bromo-2-(hydrazinecarbonyl)naphtha[2,1-b]furan-1-yl]acetamide (7), ethyl-1-acetamido-5- bromonaphtho[2,1-b]furan-2-carboxylate (6), N-(5-nitro-2-(5-phenyl-1,3,4-oxadiazol-2-yl)naphtha[2,1-bfuran-1- yl]acetamide (5),N-(2-(hydrazinecarbonyl)-5-nitronaphtho[2,1-b]furan-1-yl)acetamide (4), ethyl-1-acetamido-5- nitrpnaphtho[2,1-b]furan-2-carboxylate (3), are prepared by ethyl-1-acetamidonaphtho[2,1-b]furan-2-carboxyate and ethyl 1-aminonaphtho[2,1-b]furan-2-carboxylat

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2

Qiu, Guanyinsheng, Yuewen Li, Lele Ma, and Hongwei Zhou. "KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide." Organic Chemistry Frontiers 4, no. 6 (2017): 1069–73. http://dx.doi.org/10.1039/c6qo00840b.

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Girel, Sergey, Vadim Schütz, Laurent Bigler, Peter Dörmann, and Margot Schulz. "Bioactive Nitrosylated and Nitrated N-(2-hydroxyphenyl)acetamides and Derived Oligomers: An Alternative Pathway to 2-Amidophenol-Derived Phytotoxic Metabolites." Molecules 27, no. 15 (2022): 4786. http://dx.doi.org/10.3390/molecules27154786.

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Incubation of Aminobacter aminovorans, Paenibacillus polymyxa, and Arthrobacter MPI764 with the microbial 2-benzoxazolinone (BOA)-degradation-product 2-acetamido-phenol, produced from 2-aminophenol, led to the recently identified N-(2-hydroxy-5-nitrophenyl) acetamide, to the hitherto unknown N-(2-hydroxy-5-nitrosophenyl)acetamide, and to N-(2-hydroxy-3-nitrophenyl)acetamide. As an alternative to the formation of phenoxazinone derived from aminophenol, dimers- and trimers-transformation products have been found. Identification of the compounds was carried out by LC/HRMS and MS/MS and, for the n

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4

Gowda, Basavalinganadoddy Thimme, Jozef Kožíšek, Ingrid Svoboda, and Hartmut Fuess. "Effect of Meta-Substitution on Solid State Geometry of N-(Aryl)-2,2,2-trichloro-acetamides, 3-XC6H4NH-CO-CCl3 and 3,5-X2C6H3NH-CO-CCl3 (X = Cl, CH3)." Zeitschrift für Naturforschung A 62, no. 1-2 (2007): 91–100. http://dx.doi.org/10.1515/zna-2007-1-213.

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The crystal structures of N-(meta-substituted phenyl)-2,2,2-trichloro-acetamides such as N- (3-methylphenyl)-2,2,2-trichloro-acetamide, 3-CH3C6H4NH-CO-CCl3 (3MPTCA); N-(3-chlorophenyl)- 2,2,2-trichloro-acetamide, 3-ClC6H4NH-CO-CCl3 (3CPTCA); N-(3,5-dimethylphenyl)- 2,2,2-trichloro-acetamide, 3,5-(CH3)2C6H3NH-CO-CCl3 (35DMPTCA) and N-(3,5-dichlorophenyl)- 2,2,2-trichloro-acetamide, 3,5-Cl2C6H3NH-CO-CCl3 (35DCPTCA) have been determined at room temperature. The crystal system, space group, formula units and lattice constants (Å ) of the new structures are: 3MPTCA: orthorhombic, Pbca, Z = 8, a = 1

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Alagarsamy, Veerachamy, Viswas Raja Solomon, Mohaideen Thasthagir Sulthana, Meduri Satyasai Vijay, and Bandi Narendhar. "Design and synthesis of quinazolinyl acetamides for their analgesic and anti-inflammatory activities." Zeitschrift für Naturforschung B 70, no. 8 (2015): 597–604. http://dx.doi.org/10.1515/znb-2015-0035.

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AbstractA variety of novel 2-(substituted)-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamides were synthesized by the reaction of 2-chloro-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamide with various amines. The starting material, 2-chloro-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamide, was synthesized from anthranilic acid by the multistep process. The title compounds were investigated for analgesic, anti-inflammatory, and ulcerogenic index activities. Among those, the compound 2-(ethylamino)-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamide (V9) showed most potent analgesic and anti-inflammatory ac

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6

Eagle, Cassandra T., Nkongho Atem-Tambe, Kenneth K. Kpogo, Jennie Tan та Fredricka Quarshie. "(3-Methylbenzonitrile-κN)tetrakis(μ-N-phenylacetamidato)-κ4N:O;κ4O:N-dirhodium(II)(Rh—Rh)". Acta Crystallographica Section E Structure Reports Online 69, № 12 (2013): m639. http://dx.doi.org/10.1107/s1600536813029838.

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In the title compound, [Rh2(C8H8NO)4(C8H7N)], the four acetamidate ligands bridging the dirhodium core are arranged in a 2,2-transmanner. One RhIIatom is five-coordinate, in a distorted pyramidal geometry, while the other is six-coordinate, with a disorted octahedral geometry. For the six-coordinate RhIIatom, the axial nitrile ligand shows a non-linear Rh–nitrile coordination with an Rh—N—C bond angle of 166.4 (4)° and a nitrile N—C bond length of 1.138 (6) Å. Each unique RhIIatom is coordinated by atranspair of N atoms and atranspair of O atoms from the four acetamide ligands. The Neq—Rh—Rh—O

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Mahyavanshi, Vinay, and Sunil I. Marjadi. "Design and Synthesis of 1-(2-amino-1-(4-methoxyphenyl)ethyl) cyclohexanol Analogs as Potential Microbial Agents." International Journal of Drug Design and Discovery 2, no. 2 (2024): 474–82. https://doi.org/10.37285/ijddd.2.2.6.

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1-(2-amino-1-(4-methoxyphenyl)ethyl)cyclohexanol (1), on condensation with chloroacetyl chloride yielded 2-chloro-N-(2-(1-hydroxycyclohexyl)-2-(4-methoxyphenyl)ethyl)acetamide (2), which on amination with hydrazine hydrate yielded in turn 2-hydrazinyl-N-(2-(1-hydroxycyclohexyl)-2-(4-methoxyphenyl)ethyl)acetamide (3). Compound 3, on condensation with various aromatic aldehydes afforded a series of 2-(2-benzylidenehydrazinyl)-N-(2-(1-hydroxycyclohexyl)-2-(4-methoxyphenyl)ethyl)acetamides 4a-n, which upon dehydrative annulation in the presence of chloroacetyl chloride and triethylamine yielded 2-

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8

Chen, Xuanhua, Rongwei Guo, and Zhongyuan Zhou. "N-[3-Acetamido-1,3-bis(4-ethylphenyl)butenyl]acetamide." Acta Crystallographica Section E Structure Reports Online 58, no. 6 (2002): o671—o672. http://dx.doi.org/10.1107/s1600536802008607.

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Gowda, Basavalinganadoddy Thimme, Helmut Paulus, and Jozef Kožíšek. "Effect of Substitution on the Molecular Geometry of N-(2/3/4-Substituted-phenyl)-2,2-dichloro-acetamides, 2/3/4-XC6H4NH-CO-CHCl2 (X = CH3 or Cl)." Zeitschrift für Naturforschung A 61, no. 12 (2006): 675–82. http://dx.doi.org/10.1515/zna-2006-1210.

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2MPDCAThe effect of ring substitution on the molecular geometry of amides of the type 2/3/4-XC6H4NHCO- CHCl2 (X = CH3 or Cl) has been studied by determining the crystal structures of the compounds N-(2-methylphenyl)-2,2-dichloro-acetamide, 2-CH3C6H4NH-CO-CHCl2 (); N-(3-methylphenyl)- 2,2-dichloro-acetamide, 3-CH3C6H4NH-CO-CHCl2 (3MPDCA) and N-(3-chlorophenyl)- 2,2-dichloro-acetamide, 3-ClC6H4NH-CO-CHCl2 (3CPDCA). The results are analyzed along with our earlier crystal structures of the amides N-(phenyl)-2,2-dichloro-acetamide, C6H5NH-COCHCl2 (PDCA); N-chloro-N-(phenyl)-2,2-dichloro-acetamide,

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10

Que, Chuqiang, Peipei Huang, Zhanhui Yang, Ning Chen, and Jiaxi Xu. "Intramolecular Carbene C-H Insertion Reactions of 2-Diazo-2-sulfamoylacetamides." Molecules 24, no. 14 (2019): 2628. http://dx.doi.org/10.3390/molecules24142628.

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The intramolecular C-H insertions of carbenes derived from 2-diazo-2-sulfamoylacetamides were studied. 2-Diazo-2-sulfamoylacetamides were first prepared from chloroacetyl chloride and secondary amines through acylation followed by sequential treatments with sodium sulfite, phosphorus oxychloride, secondary amines, and 4-nitrobenzenesulfonyl azide. The results indicate that: (1) 2-diazo-N,N-dimethyl-2-(N,N-diphenylsulfamoyl)acetamide can take the formal aromatic 1,5-C-H insertion in its N-phenylsulfonamide moiety to afford the corresponding 1,3-dihydrobenzo[c]isothiazole-3-carboxamide 2,2-dioxi

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Nagarsha, K. M., T. M. Sharanakumar, D. Ramesh, M. N. Kumarswamy, and K. P. Latha. "SYNTHESIS, CHARACTERIZATION, AND ANTIBACTERIAL ACTIVITIES OF NAPHTHO[2,1-b]FURAN DERIVATIVES." RASAYAN Journal of Chemistry 15, no. 04 (2022): 2477–84. http://dx.doi.org/10.31788/rjc.2022.1548052.

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The naphthofuran and its derivatives are important biological compounds so we have focused on the synthesis of naphthofuran derivatives. The synthesized compounds of ethyl 1-(acetylamino)-5-nitronaphtho[2,1-b]furan-2- carboxylate (3), and N-[2-(hydrazinylcarbonyl)-5-nitronaphtho[2,1-b]furan-1-yl]acetamide (4) used for the synthesis of N-(2-{[(2Z)-2-benzylidenehydrazinyl]carbonyl}-5-nitronaphtho[2,1-b]furan-1-yl)acetamide compounds of four derivatives 5 (a-d) and 1-acetamido-5-nitro-N-(5-oxo-2-phenylthiazolidin-3-yl)naphtha[2,1-b]furan-2-carboxamide compounds of four derivatives 6 (a-d). The pr

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Halmi, Mohd Izuan Effendi, Mohd Badrin Hanizam Abdul Rahim, Garba Uba, and Hafeez Muhammad Yaka. "Characterization of the Growth of Pseudomonas sp. strain DrY135 on Acetamide." Bulletin of Environmental Science and Sustainable Management (e-ISSN 2716-5353) 7, no. 1 (2023): 14–18. http://dx.doi.org/10.54987/bessm.v7i1.896.

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Acetamide is heavily used as a plasticizer and stabilizer and in the methylamine manufacturing process. There has been a modest but steady rise in worldwide interest in microbe-mediated acetamide decomposition or degradation as a bioremediation method. A previously isolated molybdenum-reducing bacterium with amide-degrading capability is characterized for its growth on acetamide in this study. The bacterium growth optimally in between 500 and 1000 mg/L of acetamide, an optimal pH of between 6.5 and 8.0, and optimal temperatures supporting growth of between 30 and 35 °C. Toxic heavy metals, suc

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13

Gowda, Basavalinganadoddy Thimme, Helmut Paulus, Ingrid Svoboda, and Hartmut Fuess. "Structural Studies on N-(Phenyl)-2,2,2-trimethyl-acetamide, N-(2,4,6-Trimethylphenyl)-2,2,2-trimethyl-acetamide and N-(2,4,6-Trimethylphenyl)-2,2,2-trichloro-acetamide, 2,4,6-X3C6H2NH-CO-CY3 (X = H or CH3; Y = CH3 or Cl)." Zeitschrift für Naturforschung A 62, no. 5-6 (2007): 331–37. http://dx.doi.org/10.1515/zna-2007-5-615.

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To study the effect of side chain and ring substitutions on the solid state geometry of amides of the general formulae C6H5NH-CO-CX3 and 2,4,6-X3C6H2NH-CO-CH3−yXy (X = CH3 or Cl and y = 0,1,2, 3), crystal structures of N-(phenyl)-2,2,2-trimethyl-acetamide, C6- H5NH-CO-C(CH3)3 (PTMA); N-(2,4,6-trimethylphenyl)-2,2,2-trimethyl-acetamide, 2,4,6-(CH3)3- C6H2NH-CO-C(CH3)3 (TMPTMA) and N-(2,4,6-trimethylphenyl)-2,2,2-trichloro-acetamide, 2,4, 6-(CH3)3C6H2NH-CO-CCl3 (TMPTCA) have been determined. The data are analyzed along with those of N-(phenyl)-acetamide, C6H5NH-CO-CH3; N-(phenyl)-2,2,2-trichloro

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Sawant, Ramesh, and Deepali Kawade. "Synthesis and biological evaluation of some novel 2-phenyl benzimidazole-1-acetamide derivatives as potential anthelmintic agents." Acta Pharmaceutica 61, no. 3 (2011): 353–61. http://dx.doi.org/10.2478/v10007-011-0029-z.

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Synthesis and biological evaluation of some novel 2-phenyl benzimidazole-1-acetamide derivatives as potential anthelmintic agentsThe present study describes synthesis of a series of 2-phenyl benzimidazole-1-acetamide derivatives and their evaluation for anthelmintic activity using Indian adult earthworms,Pheretima posthuma.The structure of the title compounds was elucidated by elemental analysis and spectral data. The compounds 4-({[2-(4-nitrophenyl)-1H-benzimidazol-1-yl]acetyl}amino) benzoic acid (3a),N-ethyl-2-[2-(4-nitrophenyl)-1H-benzimidazol-1-yl] acetamide (3c),N-benzyl-2-[2-(4-nitrophen

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Dziadek, Jaroslaw, Stacey A. Rutherford, Murty V. Madiraju, Mark A. L. Atkinson, and Malini Rajagopalan. "Conditional expression of Mycobacterium smegmatis ftsZ, an essential cell division gene." Microbiology 149, no. 6 (2003): 1593–603. http://dx.doi.org/10.1099/mic.0.26023-0.

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To understand the role of Mycobacterium smegmatis ftsZ (ftsZsmeg ) in the cell division process, the ftsZ gene was characterized at the genetic level. This study shows that ftsZsmeg is an essential gene in that it can only be disrupted in a merodiploid background carrying another functional copy. Expression of ftsZsmeg in M. smegmatis from a constitutively active mycobacterial promoter resulted in lethality whereas that from a chemically inducible acetamidase (ami) promoter led to FtsZ accumulation, filamentation and cell lysis. To further understand the roles of ftsZ in cell division a condit

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Liu, L. K., F. T. Luo, and L. C. Hsieh. "Acetamide hydrochloride." Acta Crystallographica Section C Crystal Structure Communications 50, no. 8 (1994): 1333–35. http://dx.doi.org/10.1107/s0108270194001952.

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Kerridge, D. H. "The chemistry of molten acetamide and acetamide complexes." Chemical Society Reviews 17 (1988): 181. http://dx.doi.org/10.1039/cs9881700181.

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Olszewska, E., S. Pikus, and B. Tarasiuk. "New powder diffraction data of some derivatives of N-alkyl (aryl)-2,4-dichlorophenoxyacetamide—New potential pesticides." Powder Diffraction 23, no. 4 (2008): 338–49. http://dx.doi.org/10.1154/1.3009636.

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Four new derivatives of N-aryl-2,4-dichlorophenoxyacetamide, 2-(2,4-dichlorophenoxy)-N-(4-fluorophenyl)acetamide, N-(4-bromophenyl)-2-(2,4-dichlorophenoxy)acetamide, N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(2,4-dichlorophenoxy)acetamide, and N-(3-chloro-4-fluorophenyl)-2-(2,4-dichlorophenoxy)acetamide, and two of N-alkyl-2,4-dichlorophenoxyacetamide, N-dodecyl-2,4-dichlorophenoxy-acetamide and 2-(2,4-dichlorophenoxy)-N-hexadecylacetamide, have been characterized by X-ray powder diffraction. These organic compounds are potential pesticides. Experimental 2θ peaks positions, relative peak intens

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Ma, Cha, Long Li, Hu Lu, Xu Bo Yuan, and Gang Wang. "Study on the Effect of Humic Acid Acetamide on the Rheological Properties of Diesel Oil-Based Drilling Fluids." Applied Mechanics and Materials 620 (August 2014): 449–52. http://dx.doi.org/10.4028/www.scientific.net/amm.620.449.

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A new kind of humic acid acetamide compoud was synthesized by chemical modification of humic acid with octadecylamine, and the effect of humic acid acetamide on the rheological properties of oil-based drilling fluids was investigated. The results indicated that the humic acid acetamide had excellent dispersing property, and good capacity of depressing fluid loss. Moreover, the humic acid acetamide had better property of depressing fluid loss than oxidated asphalt. As a result, this humic acid acetamide is an excellent fluid loss agent for diesel oil-based drilling fluids, and is an good altern

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Olszewska, E., B. Tarasiuk, and S. Pikus. "New powder diffraction data of some derivatives of N-(hydroxyalkyl)-4-chlorophenoxyacetamide—Potential pesticides." Powder Diffraction 24, no. 4 (2009): 327–36. http://dx.doi.org/10.1154/1.3257637.

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Five new derivatives of N-(ω-hydroxyalkyl)-4-chlorophenoxyacetamide [namely, 2-(4-chlorophenoxy)-N-(2-hydroxyethyl) acetamide, 2-(4-chlorophenoxy)-N-(3-hydroxypropyl) acetamide, 2-(4-chlorophenoxy)-N-[1-(hydroxymethyl) propyl] acetamide, 2-(4-chlorophenoxy)-N-(2-hydroxy-1,1-dimethylethyl) acetamide, and 2-(4-chlorophenoxy)-N-{2-[(2-hydroxyethyl) amino] ethyl} acetamide] and one 2-(4-chlorophenoxy) acetohydrazide have been characterized by X-ray powder diffraction. These organic compounds are potential pesticides. New diffraction data including experimental and calculated 2θ peaks positions, va

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Linh, Bùi Thị Thùy, Nguyễn Tiến Công, and Huỳnh Thị Xuân Trang. "SYNTHESIS AND STRUCTURE OF SOME CHALCONES CONTAINING ACETAMIDE GROUP." Tạp chí Khoa học 17, no. 9 (2020): 1536. http://dx.doi.org/10.54607/hcmue.js.17.9.2789(2020).

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Hai chalcone là (E)-3-(2-hydroxyphenyl)-1-phenylprop-2-en-1-one (3a) và (E)-3-(4-hydroxyphenyl)-1-phenylprop-2-en-1-one (3b) đã được tổng hợp tương ứng từ phản ứng của acetophenone với 2-hydroxybenzaldehyde hoặc 4-hydroxybenzaldehyde. Phản ứng Williamson giữa (3a) hoặc (3b) với các N-aryl-2-chloroacetamide khác nhau đã tạo thành 8 hợp chất (E)-N-(4-aryl)-2-(2/4-(3-oxo-3-phenylprop-1-en-1-yl)phenoxy)acetamide; 7 trong số đó là chất mới: (E)-N-(4-bromophenyl)-2-(2-(3-oxo-3-phenylprop-1-en-1-yl)phenoxy)acetamide (5a), (E)-N-(4-chlorophenyl)-2-(2-(3-oxo-3-phenylprop-1-en-1-yl)phenoxy)acetamide (5b

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Nikolić, Ružica, and Gordana Ristić. "Activity of acetamide in acetamide-calcium nitrate melt solutions." Journal of Solution Chemistry 23, no. 7 (1994): 787–94. http://dx.doi.org/10.1007/bf00972673.

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Olszewska, E., B. Tarasiuk, and S. Pikus. "New powder diffraction data of some N-derivatives of 4-chloro-3,5-dimethylphenoxyacetamide-potential pesticides." Powder Diffraction 26, no. 4 (2011): 337–45. http://dx.doi.org/10.1154/1.3652921.

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N-derivatives of 4-chloro-3,5-dimethylphenoxyacetamide—2-(4-chloro-3,5-dimethylphenoxy)-N-(4-fluorophenyl)acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-(3-chloro-4-fluorophenyl) acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-[4-chloro-3-(trifluoromethyl)phenyl] acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-[3-chloro-4-methylphenyl]acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-(2,4,6-tribromophenyl) acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-pyridin-2-ylacetamide, 1-[(4-chloro-3,5-dimethylphenoxy)acetyl]-4-methylpiperazine, and 1-benzyl-4-[(4-chloro-3,5-dimethylphenoxy)acetyl]piperazine—have

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Gowda, B. Thimme, Sabine Foro, and Hartmut Fuess. "2-Chloro-N-(4-chlorophenyl)acetamide." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4488. http://dx.doi.org/10.1107/s1600536807053093.

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The structure of the title compound, C8H7Cl2NO, resembles those of N-(4-chlorophenyl)acetamide, N-2-chloro-(4-methylphenyl)acetamide, N-2-chloro-(4-nitrophenyl)acetamide and other related amides, with similar bond parameters. Molecules are linked into chains through N—H...O hydrogen bonding.

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Çankaya, Nevin, Serap Yalcin, and Fahriye Ercan. "In Vivo and in Silico Evaluation of the Effect of p-Acetamide and MPAEMA on the Model Organism Galleria Mellonella (Lepidoptera: Pyralidae)." Kahramanmaraş Sütçü İmam Üniversitesi Tarım ve Doğa Dergisi 28, no. 3 (2025): 625–35. https://doi.org/10.18016/ksutarimdoga.vi.1591091.

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In this study, 2-chloro-N-(4-methoxyphenyl)acetamide (p-acetamide) and 2-(4-methoxyphenylamino)-2-oxoethyl methacrylate (MPAEMA) were resynthesized to evaluate their effect on the agricultural pest Galleria mellonella. The toxicities of p-acetamide and MPAEMA against the larval stage of G. mellonella were evaluated concurrently. The results indicate that p-acetamide has a lethal effect on insect larvae at lower doses. LC50 doses of p-acetamide and MPAEMA were 873,572 and 687,355 uM, respectively. These values represent the concentrations of the substances at which 50% of the larvae exposed to

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Jiang, Jikang, Haixia Ye, Jingfei Zhou, Chenlu Wang, Zheng Shen, and Yalei Zhang. "Research and Mechanism of Two-step Preparation of Acetamide from Microalgae under Hydrothermal Conditions." E3S Web of Conferences 194 (2020): 02006. http://dx.doi.org/10.1051/e3sconf/202019402006.

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A two-step synthesis of acetamide under hydrothermal condition from microalgae, is presented. results showed that the best yield of acetamide and selectivity of acetic acid were 9.5 % and 60.1 % at 320 ℃ for 8 min with a NH3 supply of 30. Algae such as spirulina, cyanobacteria and autotrophic chlorella could also acquire acetamide, and lactic acid was found to be an important intermediate during the exploration of reaction pathways. These results demonstrated that it is possible to develop a process for conversion of microalgae biomass into acetamide.

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Narayana, Badiadka, Hemmige S. Yathirajan, Ravindranath Rathore, and Christopher Glidewell. "Crystal structures of two C,N-disubstituted acetamides: 2-(4-chlorophenyl)-N-(2-iodophenyl)acetamide and 2-(4-chlorophenyl)-N-(pyrazin-2-yl)acetamide." Acta Crystallographica Section E Crystallographic Communications 72, no. 9 (2016): 1270–75. http://dx.doi.org/10.1107/s2056989016012512.

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In the crystal of 2-(4-chlorophenyl)-N-(2-iodophenyl)acetamide, C14H11ClINO, molecules are linked by a combination of N—H...O and C—H...O hydrogen bonds to form aC(4)C(4)[R21(7)] chain of rings and chains of this type are linked by a combination of C—Cl...π(arene) and C—I...π(arene) interactions to form deeply puckered twofold interwoven sheets. In the crystal of 2-(4-chlorophenyl)-N-(pyrazin-2-yl)acetamide, C12H10ClN3O, molecules are linked into complex sheets by N—H...N, C—H...N and C—H...O hydrogen bonds, and by C—H...π(arene) interactions.

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Yu, Jia, Xuan Chen, Xiaoliang Ma, Qingfei Song, Yukun Zhao, and Jiahao Cao. "Influence of Nanoparticles and Graphite Foam on the Supercooling of Acetamide." Journal of Nanomaterials 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/313674.

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Acetamide is a promising phase change materials (PCMs) for thermal storage,but the large supercooling during the freezing process has limited its application. In this study, we prepared acetamide-SiO2composites by adding nano-SiO2into acetamide. This modified PCM was then impregnated into the porous graphite foam forming acetamide-SiO2-graphite foam form-stable composites. These composites were subjected to melting-solidification cycles 50 times; the time-temperature curves were tracked and recorded during these cycles. The time-temperature curves showed that, for the acetamide containing 2 wt

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Gowda, B. Thimme, Sabine Foro, P. G. Nirmala, and Hartmut Fuess. "N-(Phenylsulfonyl)acetamide." Acta Crystallographica Section E Structure Reports Online 66, no. 6 (2010): o1284. http://dx.doi.org/10.1107/s1600536810015849.

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Pei, Wen, Li Sun, Yueshui Shao, and Dongwei Li. "2-(Benzhydrylsulfinyl)acetamide." Acta Crystallographica Section E Structure Reports Online 60, no. 3 (2004): o372—o373. http://dx.doi.org/10.1107/s1600536804001382.

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Castellani, F., G. Berchiesi, and V. Bartocci. "Acetamide-ammonium sulfamate." Journal of Thermal Analysis 36, no. 3 (1990): 1071–76. http://dx.doi.org/10.1007/bf01904644.

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Wang, Hong, Dong Yuan Jin, Zhi Qiang Yang, Yong Hong Gao, Jian Wei Tao, and Li Hua Li. "Synthesis of Phenoxy Amide Derivatives." Advanced Materials Research 396-398 (November 2011): 2318–21. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.2318.

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Several kinds of new derivatives of N-substituted-4-(p-chlorophenoxy)acetamide and N-substituted-2,4-dichlorophenoxy acetamide were synthesized with methyl chloroacetate. The influence of solvent on the chlorination occurred in the benzene ring of phenoxy acetamide additives has been investigated by using sulfonyl chloride as chlorination agent. Result shows that the higher polarity of solvent is beneficial to the chlorination.

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Zikmundová, M., K. Drandarov, L. Bigler, M. Hesse, and C. Werner. "Biotransformation of 2-Benzoxazolinone and 2-Hydroxy-1,4-Benzoxazin-3-one by Endophytic Fungi Isolated from Aphelandra tetragona." Applied and Environmental Microbiology 68, no. 10 (2002): 4863–70. http://dx.doi.org/10.1128/aem.68.10.4863-4870.2002.

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ABSTRACT The biotransformation of the phytoanticipins 2-benzoxazolinone (BOA) and 2-hydroxy-1,4-benzoxazin-3-one (HBOA) by four endophytic fungi isolated from Aphelandra tetragona was studied. Using high-performance liquid chromatography-mass spectrometry, several new products of acylation, oxidation, reduction, hydrolysis, and nitration were identified. Fusarium sambucinum detoxified BOA and HBOA to N-(2-hydroxyphenyl)malonamic acid. Plectosporium tabacinum, Gliocladium cibotii, and Chaetosphaeria sp. transformed HBOA to 2-hydroxy-N-(2-hydroxyphenyl)acetamide, N-(2-hydroxyphenyl)acetamide, N-

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Sharma, Manu, Harikrishnan K, Umesh Kumar Gaur, and Ashok K. Ganguli. "Synthesis of mesoporous SiO₂–CeO₂ hybrid nanostructures with high catalytic activity for transamidation reaction." RSC Advances 13, no. 19 (2023): 13134–41. http://dx.doi.org/10.1039/d3ra01552a.

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35

El Kayal, Wassim, Hanna Severina, Vadim Tsyvunin, et al. "Synthesis and anticonvulsant activity evaluation of n-[(2,4-dichlorophenyl)methyl]-2-(2,4-dioxo-1h-quinazolin-3-yl)acetamide novel 1-benzylsubstituted derivatives." ScienceRise: Pharmaceutical Science, no. 1(35) (February 28, 2022): 58–69. http://dx.doi.org/10.15587/2519-4852.2022.253554.

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The aim. Synthesis of 1-benzylsubstituted derivatives of N-[(2,4-dichlorophenyl)methyl]-2-(2,4-dioxo-1h-quinazolin-3-yl)acetamide, and determination of affinity to GABAergic biotargets with the following anticonvulsant activity estimation using PTZ-induced seizures model in mice. Materials and methods. Standard organic synthesis methods were used; the structure of the synthesized compounds was proved by elemental analysis, 1H and 13C NMR spectroscopy, and LC/MS method; composition of the synthesized compounds – by elemental analysis, their individuality – by TLC and LC/MS methods. AutoDo

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Kong, Youqing, Bin Ye, Lei Yang, Xiangnong Liu, and Cai Gao. "Comparative Molecular Dynamics Study On Interaction Of Acetamide And Glycerol With Phospholipid Bilayer." Cryoletters 43, no. 1 (2022): 42–49. http://dx.doi.org/10.54680/fr22110110412.

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BACKGROUND: The exact mechanisms that acetamide and glycerol interact with cell membrane remains a matter of debate. OBJECTIVE: To investigate the microscopic interactions of acetamide and glycerol with phospholipid bilayers at various temperatures. MATERIALS AND METHODS: Molecular dynamics simulations of a hydrated dipalmitoyl-phosphatidylcholine (DPPC) bilayer in the presence of glycerol and acetamide were performed. The system contains 128 lipids and about 700 cryoprotectant molecules, and simulations extended to 15 ns. RESULT: When compared to glycerol, acetamide shows a stronger affinity

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Nakamura, Kenji, Yuji Ishii, Shinji Takasu, Takehiko Nohmi, Makoto Shibutani, and Kumiko Ogawa. "Lack of In Vivo Mutagenicity of Acetamide in a 13-Week Comprehensive Toxicity Study Using F344 gpt Delta Rats." Toxicological Sciences 177, no. 2 (2020): 431–40. http://dx.doi.org/10.1093/toxsci/kfaa126.

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Abstract Acetamide, a food contaminant, has been shown to induce hepatocellular tumors in rats. However, the mode of action underlying acetamide-induced hepatocarcinogenesis remains unclear. In the current study, we aimed to examine the possible involvement of in vivo mutagenicity in hepatocarcinogenesis of acetamide and evaluate its toxicological profile using a comprehensive medium-term toxicity study in gpt delta rats. Six-week-old male F344 gpt delta rats were given a basal diet containing 0%, 0.625%, 1.25%, or 2.5% acetamide for 13 weeks. In general toxicologic assessment, hepatotoxic par

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Patel, Romil, and Vikram Patel. "Experimental Analysis of Scheffler Reflector-Based Solar Cooking System: An Application of Sensible and Latent Heat Storage Materials." Jurnal Kejuruteraan 36, no. 4 (2024): 1505–18. http://dx.doi.org/10.17576/jkukm-2024-36(4)-16.

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Solar cooker with different collector like evacuated tubes collector, parabolic trough collector, flat plate collector, and Scheffler reflector collector etc are generally used for the cooking food with SHSMs or PCMs. Present research article, Scheffler reflector with combined heat storage material (one SHSM and one PCM) for late-evening cooking has been experimentally investigated. One material is placed within the inner pot of a solar cooker, while another material is placed outer pot of the solar cooker. Six combinations are formed from various SHSMs (sand, pebbles, and iron pieces) and PCM

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Riya S. Tumram, Urvashi P. Manik, and Paritosh L. Mishra. "Analysis of thermo-acoustic parameters in view to obtain the interaction between acetamide in some salt solutions at different temperature." Magna Scientia Advanced Research and Reviews 10, no. 2 (2024): 165–72. http://dx.doi.org/10.30574/msarr.2024.10.2.0054.

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The ultrasonic velocity and density have been calculated for acetamide in the solution NaCl and KCl at different temperatures (viz. 283, 288,293,298K) for various concentrations from 0.02-0.2mol/kg thermodynamic and sound parameters such as adiabatic compressibility, acoustic impedance, relative association, internal pressure, available volume, specific heat ration, relaxation strength, isothermal compressibility, molecular radius, surface tension, enthalpy, Rao’s constant, Wada’s constant, free length, have been gained from research examination for the (Acetamide +H2O/NaCl/KCl). To investigat

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Narayana, V. V. P. C., K. Sajitha, V. Bala Yesu, et al. "Synthesis of some new pyridine-acetamide hybrids as potential antibacterial and antioxidant agents." INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY 35, no. 02 (2025): 237. https://doi.org/10.59467/ijhc.2025.35.237.

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The present study reports the synthesis of two new series of pyridine-acetamide hybrid derivatives, 6a-e and 13a-e and their evaluation of antibacterial and antioxidant properties. The synthesis involved acylating pyridinylamines with chloroacetyl chloride to form corresponding 2-chloro-N-pyrdinylacetamides, which were then reacted with various secondary amines to yield pyridine-acetamide hybrid derivatives. Compounds 6b and 6e showed the highest efficacy comparable to the standard antibiotic, azithromycin. Compound 6b showed the highest antioxidant potential, with IC50 of 66.2 μg/mL and compo

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Guo, Sheng, De Yi Huang, Ji Feng She, and Xiang Qun Liang. "Comparison Activating Ability of Three Hydrogen Peroxide Activators." Advanced Materials Research 641-642 (January 2013): 215–18. http://dx.doi.org/10.4028/www.scientific.net/amr.641-642.215.

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The bleaching efficiency of hydrogen peroxide can be promoted by using suitable activator. In our research, two methods were applied to compare the activating ability of three activators, TAED (tetraacetylethylenediamine), acetamide and dicyandiamide. The first part was hydrogen peroxide bleaching. TAED was excellent, because the brightness improvement was the maximum; the viscosity was acceptable. Acetamide was an applied activator in peroxide bleaching，for it could get same effects as TAED if the bleaching process had enough time and enough dosage. In the last part our study was about the ki

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Wassim, El Kayal, Severina Hanna, Tsyvunin Vadim, et al. "Synthesis and anticonvulsant activity evaluation of n-[(2,4-dichlorophenyl)methyl]-2-(2,4-dioxo-1h-quinazolin-3-yl)acetamide novel 1-benzylsubstituted derivatives." ScienceRise: Pharmaceutical Science, no. 1(35) (February 28, 2022): 58–69. https://doi.org/10.15587/2519-4852.2022.253554.

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<strong>The aim</strong>. Synthesis of 1-benzylsubstituted derivatives of N-[(2,4-dichlorophenyl)methyl]-2-(2,4-dioxo-1h-quinazolin-3-yl)acetamide, and determination of affinity to GABAergic biotargets with the following anticonvulsant activity estimation using PTZ-induced seizures model in mice. <strong>Materials and methods</strong>. Standard organic synthesis methods were used; the structure of the synthesized compounds was proved by elemental analysis, <sup>1</sup>H and <sup>13</sup>C NMR spectroscopy, and LC/MS method; composition of the synthesized compounds – by elementa

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Ravi Kumar, Gollapudi, Chandra Mohan Kurmarayuni, Manideepa Indupalli, Ramya Krishna Pallapati, and Hari Babu Bollikolla. "Synthesis of new analogs of 3-methyl-[1,2,4] triazolo [3,4-a] phthalazines via Suzuki coupling and evaluation of their anticancer and antimicrobial activity." Mediterranean Journal of Chemistry 8, no. 4 (2019): 261–69. http://dx.doi.org/10.13171/mjc841905257hbb.

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A series of new N-aryl substituted phenyl acetamide analogs of 3-methyl-[1,2,4] triazolo[3,4-a] phthalazines were synthesized starting from commercially available, in-expensive phthalic anhydride in good yields (65-75 %) via Suzuki Coupling. These compounds were tested for inhibition activity against HCT 116 cancer cell line by using MIT assay. Among the library of compounds, N-(3-methoxyphenyl)-2-(4-(3-methyl-[1,2,4]triazolo[3,4-a]phthalazin-6-yl)phenyl) acetamide followed by 2-(4-(3-methyl-[1,2,4]triazolo[3,4-a]phthalazin-6-yl)phenyl)-N-(m-tolyl) acetamide and Â N-(3-chlorophenyl)-2-(4-(3-me

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Arora, Pankaj Kumar, Kartik Dhar, Rafael Alejandro Veloz García, and Ashutosh Sharma. "Biotransformation of Indole to 3-Methylindole byLysinibacillus xylanilyticusStrain MA." Journal of Chemistry 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/425329.

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An indole-biotransforming strain MA was identified asLysinibacillus xylanilyticuson the basis of the 16S rRNA gene sequencing. It transforms indole completely from the broth culture in the presence of an additional carbon source (i.e., sodium succinate). Gas-chromatography-mass spectrometry identified indole-3-acetamide, indole-3-acetic acid, and 3-methylindole as transformation products. Tryptophan-2-monooxygenase activity was detected in the crude extracts of indole-induced cells of strain MA, which confirms the formation of indole-3-acetamide from tryptophan in the degradation pathway of in

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Dr., H. D. Chaudhari, and Haresh R.Patel Dr. "Chemical kinetic of Dy3+ rare metal Complex with Benzoxazole Derivative." International Journal of Interdisciplinary Research and Innovations 10, no. 4 (2022): 40–45. https://doi.org/10.5281/zenodo.7320022.

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<strong>Abstract:</strong> The combination of some rare metal ions with an important 2-(1,3-benzoxazole -2-yl - sulfanyl )-N-phenyl acetamide (BSPA) ligand to form coordination compounds is an important area of current research. Less explored biologically important 2-(1,3-benzoxazole -2-yl - sulfanyl )-N-phenyl acetamide  ligand is allowed to react with solution of some rare metal perchlorates and attempt has been made to synthesize solid  2-(1,3-benzoxazole -2-yl- sulfanyl )-N-phenyl acetamide complexes. These 2-(1,3-benzoxazole-2-yl-sulfanyl )-N-phenyl acetamide  complexes are

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Dr., H. D. Chaudhari, and Haresh R.Patel Dr. "Chemical kinetic activity of Iridium rare metal Complex with Banzoxazole Derivative." International Journal of Life Sciences Research 12, no. 4 (2024): 1–4. https://doi.org/10.5281/zenodo.13902116.

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<strong>Abstract:</strong> The combination of Iridium rare metal ions with an important 2-(1,3-benzoxazole -2-yl - sulfanyl )-N-phenyl acetamide (BSPA) ligand to form coordination compounds is an important area of current research. Less explored biologically important 2-(1,3-benzoxazole -2-yl - sulfanyl )-N-phenyl acetamide  ligand is allowed to react with solution of some rare metal perchlorates and attempt has been made to synthesize solid  2-(1,3-benzoxazole -2-yl- sulfanyl )-N-phenyl acetamide complexes. These 2-(1,3-benzoxazole-2-yl-sulfanyl )-N-phenyl acetamide  complexes

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Natalia, Chalenko, Demchenko Anatoly, and Syrova Ganna. "Synthesis of potential antiexudative preparations for 2-((4-amino-5-(furan-2-il)-1,2,4-triazole-(4H)-3-yl)-sulfanyl)-N-acetamide series." ScienceRise: Pharmaceutical Science, no. 3(19) (June 28, 2019): 22–29. https://doi.org/10.15587/2519-4852.2019.171878.

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<strong>Aim.</strong> Conduct the purposeful synthesis of new potential biologically active substances of derivatives of 2 - ((4-amino-5- (furan-2-yl) -1,2,4-triazol (4H) -3-yl) -sulfanyl) -N-acetamides and evaluate their anti-exudative activity on the model of formalin edema in rats. <strong>Materials and methods.</strong> In this work, standard methods of organic synthesis, physical and chemical methods of proofing the structure of synthesized compounds, elemental analysis, <sup>1</sup>H NMR spectroscopy, chromatographic mass spectrometry, and antiexudative activity were studi

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Gowda, B. Thimme, Jozef Kožíšek, Miroslav Tokarčík, and Hartmut Fuess. "N-(2-Methylphenyl)acetamide." Acta Crystallographica Section E Structure Reports Online 63, no. 4 (2007): o1977—o1978. http://dx.doi.org/10.1107/s1600536807012998.

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Gowda, B. Thimme, Sabine Foro, and Hartmut Fuess. "N-(3,5-Dichlorophenyl)acetamide." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2341—o2342. http://dx.doi.org/10.1107/s1600536807015280.

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Gowda, B. Thimme, Sabine Foro, Hiromitsu Terao, and Hartmut Fuess. "N-(2,3-Dimethylphenyl)acetamide." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (2009): o964. http://dx.doi.org/10.1107/s1600536809011891.

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