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Relevant bibliographies by topics / 2-chloroacetamide

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Academic literature on the topic '2-chloroacetamide'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "2-chloroacetamide"

1

Gowda, B. Thimme, D. Krishna Bhat, H. Fuess, and Al Weiss. "35NQR Spectra of Substituted N-(phenyl)-2-chloroacetamides." Zeitschrift für Naturforschung A 54, no. 12 (1999): 679–84. http://dx.doi.org/10.1515/zna-1999-1203.

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Fifteen methyl-, nitro-, or mixed substituted N-(phenyl)-2-chloroacetamides were investigated by 35Cl NQR. The temperature dependence of the frequencies of the 3-methylphenyl and 2,6-dimethylphenyl derivatives were studied for the range 77 K<T<300 K. Only one ω C-Cl frequency was observed for the compound with the two exceptions. For N-(2-nitro,4-chlorophenyl)-2-chloroacetamide the observed values of 35.623 and 35.350 MHz were assigned to ω C-Cl and ring C-Cl, whereas the corresponding values are 36.254 and 34.815 MHz for N-(2-methyl, 3-chlorophenyl)-2-chloroacetamide. The experimental f

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2

Hulinská, Hana, Zdeněk Polívka, Jiří Jílek, et al. "Experimental antiulcer agents: N-substituted 2-(4-methyl-1-piperazinyl)acetamides as pirenzepine models and some related compounds." Collection of Czechoslovak Chemical Communications 53, no. 8 (1988): 1820–44. http://dx.doi.org/10.1135/cccc19881820.

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Reactions of N-cyclohexyl-2-chloroacetamide, N-phenyl-2-chloroacetamide, N-(4-dimethylaminophenyl)-2-chloroacetamide, N-(2-nitrophenyl)-N-phenyl-2-chloroacetamide, its 3-nitrophenyl and 4-nitrophenyl analogues, N-(2-benzylphenyl)-2-chloroacetamide, 5-(chloroacetyl)-dibenz[b,f]azepine, and its 10,11-dihydro derivative with piperazine, 1-methylpiperazine, 2-(1-piperazinyl)ethanol, and 3-(1-piperazinyl)propanol resulted in compounds II, III, V-XV, XVIII, XXI, and XXIII, simple analogues of the antiulcer agent pirenzepine (I). Contributions to the syntheses and characterization of mianserin (XIX),

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3

Malathy Sony, S. M., P. Charles, M. N. Ponnuswamy, and M. Nethaji. "N-(2-Benzoyl-4-chlorophenyl)-2-chloroacetamide." Acta Crystallographica Section E Structure Reports Online 61, no. 3 (2005): o632—o634. http://dx.doi.org/10.1107/s1600536805002291.

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Onajole, Oluseye K., Thavendran Govender, Hendrik G. Kruger, and Glenn E. M. Maguire. "N-(Adamantan-1-yl)-2-chloroacetamide." Acta Crystallographica Section E Structure Reports Online 67, no. 6 (2011): o1444. http://dx.doi.org/10.1107/s1600536811018046.

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5

Dong, Hui-Chao. "N-[2-(1,3-Benzodioxol-5-yl)ethyl]-2-chloroacetamide." Acta Crystallographica Section E Structure Reports Online 64, no. 6 (2008): o1118. http://dx.doi.org/10.1107/s1600536808014232.

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6

S. Mehdhar, Fatima, Abdullah Y. A. Alzahrani, Ebrahim Abdel-Galil, Ghada E. Abdel-Ghani, Ali Saeed, and Ehab Abdel-Latif. "Synthesis of some new thiophene-based compounds and evaluations of their cytotoxic activities." Bulletin of the Chemical Society of Ethiopia 37, no. 2 (2022): 373–89. http://dx.doi.org/10.4314/bcse.v37i2.10.

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ABSTRACT. A series of new thiophene derivatives was prepared through nucleophilic substitution reactions of the precursor N-(4-substituted-phenyl)-5-(2-chloroacetamido)-4-cyano-3-methylthiophene-2-‎carboxamides 4a and 4b with different sulfur and/or nitrogen nucleophilic reagents (namely; mercaptoacetic acid, 2-mercaptobenzothiazole, 5-(phenylamino)-1,3,4-thiadiazole-2-thiol, 2-mercapto-4,6-dimethylnicotinonitrile, 3-arylazo-4-mercapto-4-(phenylamino)-but-3-en-one derivatives, ammonium thiocyanate, piperidine and/or morpholine). The structures of the prepared thiophene compounds were character

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7

Gowda, B. Thimme, I. Svoboda, and Hartmut Fuessa. "Structural Studies on N-(2,4,5-trichlorophenyl)-2-Chloro- and 2,2,2-trichloroacetamides and N-Chloro-N-(2,4,5-trichlorophenyl)-2-Chloroacetamide." Zeitschrift für Naturforschung A 59, no. 11 (2004): 845–52. http://dx.doi.org/10.1515/zna-2004-1120.

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The effect of N-chloro, side chain and sites of ring substitutions on the crystal structure of N-(trichlorophenyl)-2-chloro and 2,2,2-trichloroacetamides has been studied by determining the crystal structure of N-(2,4,5-trichlorophenyl)-2-chloroacetamide, 2,4,5-Cl3C6H2.NHCO.CH2Cl (N245TCPCA), N-chloro-N-(2,4,5-trichlorophenyl)-2-chloroacetamide, 2,4,5-Cl3C6H2.NClCO. CH2Cl (NC245TCPCA) and N-(2,4,5-trichlorophenyl)-2,2,2-trichloroacetamide, 2,4,5-Cl3C6H2. NHCO.CCl3 (N245TCPTCA). The crystal type, space group, formula units and lattice constants in Å are: N245TCPCA: monoclinic, P21/n, Z = 4, a =

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8

Gowda, B. Thimme, I. Svoboda, and Hartmut Fuess. "Structural Studies of N-(2,4,6-trisubstitutedphenyl)-Chloroacetamides, 2,4,6-X3C6 H2 -NHCO-CH3_y Cly, (X = CH3 or Cl and y = 1 -3)." Zeitschrift für Naturforschung A 55, no. 9-10 (2000): 779–90. http://dx.doi.org/10.1515/zna-2000-9-1007.

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The effect of side chain and ring substitutions on the crystal structures of N-(2,4,6-substitutedpheny)- chloroacetamides of the type, 2,4,6-X3C6H2-NHCO-CH3_yCly (X = CH3 or Cl and 1 ⩽ y ⩽ 3), has been studied by determining the crystal structures of N-(2,4,6-trimethylphenyl)- 2-chloroacetamide, 2,4,6-(CH3)3C6H2-NHCO-CH2Cl (TMPMCA); N-(2,4,6-trichlorophenyl)-2- chloroacetamide, 2,4,6-Cl3C6H2-NHCO-CH2Cl (TCPMCA); N-(2,4,6-trichlorophenyl)-2,2-dichloroacetamide, 2,4,6-Cl3C6H2-NHCO-CHCl2 (TCPDCA) and N-(2,4,6-trichlorophenyl)-2,2,2- trichloroacetamide, 2,4,6-Cl3C6H2-NHCO-CCl3 (TCPTCA). The crysta

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9

Khalaf, N., E. Abdel-Latif, M. Ismail, and H. Metwally. "Utilisation of bis-chloroacetamide derivative in the synthesis of new biologically active sulfide compounds." South African Journal of Chemistry 76 (2022): 97–101. http://dx.doi.org/10.17159/0379-4350/2021/v76a14.

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4-Aminobenzohydrazide (1) undergoes chloroacetylation twice, at the primary amine and hydrazide-NH2 functional groups. The conforming bis-chloroacetamide derivative 3 was reacted with different sulfur reagents (namely, 2-mercaptobenzothiazole, 6-amino-2-mercaptopyrimidin-4-ol, and 2-mercapto-4,6-dimethyl-nicotinonitrile) to give new bis-sulfide compounds 5, 7 and 9, respectively. The newly synthesised bis-chloroacetamide and corresponding sulfides were screened for anti-microbial and antioxidant potential. The sulfide derivative 7 exhibited the most potent activity against Staphylococcus aureu

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10

Tariq, Javaria, Shahzad Murtaza, Muhammad Nawaz Tahir, and Muhammad Zaheer. "Crystal structure ofN,N′-(1,2-phenylene)bis(2-chloroacetamide)." Acta Crystallographica Section E Crystallographic Communications 71, no. 2 (2015): o108. http://dx.doi.org/10.1107/s2056989015000304.

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In the title compound, C10H10Cl2N2O2, the secondary amide groups are differently twisted relative to the benzene ring, with dihedral angles between the respective planes of 21.03 (2) and 81.22 (2)°. In the crystal, the molecules are connected by N—H...O and C—H...O hydrogen bonds, forming a two-dimensional polymeric network parallel to (001). One of the amide carbonyl O atoms accepts two H atoms in N—H...O and C—H...O interactions, forming anR22(6) ring motif.

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Dissertations / Theses on the topic "2-chloroacetamide"

1

Serry, F. M. El-S. "Studies on the mode of antibacterial action of 2-chloroacetamide." Thesis, University of Nottingham, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.371138.

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Book chapters on the topic "2-chloroacetamide"

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Demaison, J. "180 C2H4ClNO 2-Chloroacetamide." In Asymmetric Top Molecules. Part 1. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10371-1_182.

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2

Camp, J. E. "By Bischler–Napieralski Cyclodehydration of -(2-Benzylphenyl)-2-chloroacetamide." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00098.

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3

Kantlehner, W. "Synthesis from -Aryl-2-chloroacetamides and Malononitrile." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00574.

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Conference papers on the topic "2-chloroacetamide"

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Chitra, R., R. R. Choudhury, Frederic Capet, and Pascal Roussel. "The oxalic acid: 2-chloroacetamide crystallization: A new revelation." In SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4791310.

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