Relevant bibliographies by topics / Acetanilide

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Academic literature on the topic 'Acetanilide'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Acetanilide"

1

Antonysakthi, S., M. S. Selvakumar, and P. L. Prabha. "Electroorganic Synthesis and Characterization of 4-Ethoxy Acetanilide using Platinum and Graphite as Anodes." Journal of Scientific Research 14, no. 2 (2022): 583–91. http://dx.doi.org/10.3329/jsr.v14i2.54735.

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Alkoxy group substituted compounds of acetanilide are found to have pharmacological and industrial importance. Synthesis of alkoxy substituted acetanilides via conventional thermal methods involves multi-step processes, formation of side products, and the poor yield of desired products. But, the vast literature studies reveal that electroorganic synthesis of alkoxy substituted acetanilide derivatives would be effectively carried out through electrochemical oxidation methods. The direct substitution of the ethoxy (alkoxy) group onto the aromatic ring, an electrophilic substitution, has not been
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FUJIMOTO, Takeo. "Acetanilide." Journal of Synthetic Organic Chemistry, Japan 50, no. 2 (1992): 172–73. http://dx.doi.org/10.5059/yukigoseikyokaishi.50.172.

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Zouied, Daoiya, Emna Zouaoui, Mohamed Salah Medjram, Olfa Chikha, and Karima Dob. "The para hydroxy acetanilide and acetanilide mixture for the protection from corrosion of alloyed zinc." Anti-Corrosion Methods and Materials 65, no. 1 (2018): 1–10. http://dx.doi.org/10.1108/acmm-02-2017-1754.

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Purpose Corrosion and corrosion inhibition of alloyed zinc electrode were investigated in neutral chloride solution using electrochemical techniques. The purpose of this study is to study the corrosion inhibition of acetanilide and para hydroxy acetanilide as organics inhibitors for corrosion control of alloyed zinc electrode in NaCl 3 per cent solution. Design/methodology/approach A volt lab PGZ 301, assembled using alloyed zinc working electrode, a platinum counter electrode and a saturated calomel electrode as the reference electrode, was used in the experiment. This research was conducted
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Singh, Rajib K., Arvind Kumar, and Arun K. Mishra. "Chemistry and Pharmacology of Acetanilide Derivatives: A Mini Review." Letters in Organic Chemistry 16, no. 1 (2018): 6–15. http://dx.doi.org/10.2174/1570178615666180808120658.

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Acetanilide or N-phenylacetamide is an aromatic compound having phenyl ring attached to an acetamido group (–NHCOCH3). In 1886, acetanilide was introduced as an analgesic and antipyretic drug into medical practice by A. Cahn and P. Hepp. Since then, many acetanilide derivatives have been found to have antimicrobial, analgesic, anti-inflammatory, antipyretic, antioxidant, anticonvulsant, anti- cancer, antihyperglycaemic and antimalarial activities. Acetanilide also plays an important role in the synthesis of a number of chemicals as intermediates and precursors. The chief objective of the prese
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JALILI, SEIFOLLAH, and MOJDEH AKHAVAN. "STUDY OF INTRAMOLECULAR HYDROGEN BONDING IN ORTHO-SUBSTITUTED ACETANILIDE COMPOUNDS USING COMPUTATIONAL METHODS." Journal of Theoretical and Computational Chemistry 03, no. 04 (2004): 527–42. http://dx.doi.org/10.1142/s0219633604001185.

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The intramolecular hydrogen bonding formation in ortho-substituted compounds of Acetanilide, ortho-hydroxy Acetanilide and ortho-nitro Acetanilide, was investigated using Density Functional Theory (DFT), Møller-Plesset second-order (MP2) method and "Atoms in Molecules (AIM)" theory. It was found that in each case, the cis isomer is more stable than the trans isomer and ortho-nitro Acetanilide forms a stronger hydrogen bond than ortho-hydroxy Acetanilide. The effects of hydrogen bonding on structural parameters of the considered systems were studied using Becke's functional (B3LYP) and at the a
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Bellinder, Robin R., and Donald T. Warholic. "Evaluation of Acetanilide Injury and Its Potential for Yield Reduction in Cabbage,Brassica oleraceaL." Weed Technology 2, no. 3 (1988): 350–54. http://dx.doi.org/10.1017/s0890037x00030724.

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Field studies were conducted from 1984 to 1986 to assess cabbage injury and yield response to several acetanilide herbicides. When incorporated, metolachlor significantly injured cabbage and reduced yields while post-transplant applications caused foliar flecking but did not reduce yields. Crop injury from pretransplant applications of 4.4 kg ai/ha was significant for all herbicides in both 1985 and 1986. Although total yields in 1985 and 1986 were comparable, maturity was delayed in 1986. With few exceptions, the acetanilides did not differ in either injury or yield-reducing potential. Howeve
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Shoemaker, Jody A. "Novel Chromatographic Separation and Carbon Solid-Phase Extraction of Acetanilide Herbicide Degradation Products." Journal of AOAC INTERNATIONAL 85, no. 6 (2002): 1331–37. http://dx.doi.org/10.1093/jaoac/85.6.1331.

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Abstract One acetamide and 5 acetanilide herbicides are currently registered for use in the United States. Over the past several years, ethanesulfonic acid (ESA) and oxanilic acid (OA) degradation products of these acetanilide/acetamide herbicides have been found in U.S. ground waters and surface waters. Alachlor ESA and other acetanilide degradation products are listed on the U.S. Environmental Protection Agency's (EPA) 1998 Drinking Water Contaminant Candidate List. Consequently, EPA is interested in obtaining national occurrence data for these contaminants in drinking water. EPA currently d
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PANG, XIAO-FENG, and XIANG-RONG CHEN. "STUDY ON PROPERTIES OF ENERGY SPECTRA OF THE MOLECULAR CRYSTALS." International Journal of Modern Physics B 20, no. 18 (2006): 2505–15. http://dx.doi.org/10.1142/s0217979206034820.

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The energy-spectra of nonlinear vibration of molecular crystals such as acetanilide have been calculated by using discrete nonlinear Schrödinger equation appropriate to the systems, containing various interactions. The energy levels including higher excited states are basically consistent with experimental values obtained by infrared absorption and Raman scattering in acetanilide. We further give the features of distribution of the energy-spectra for the acetanilide. Using the energy spectra we also explained well experimental results obtained by Careri et al..
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Scott, Alwyn C., Irving J. Bigio, and Clifford T. Johnston. "Polarons in acetanilide." Physical Review B 39, no. 17 (1989): 12883–87. http://dx.doi.org/10.1103/physrevb.39.12883.

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Schatz, Paul F. "Bromination of Acetanilide." Journal of Chemical Education 73, no. 3 (1996): 267. http://dx.doi.org/10.1021/ed073p267.

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Dissertations / Theses on the topic "Acetanilide"

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Coles, L. Susanne. "The acetanilide crystal structures : packing and conformational similarities." Thesis, University of Southampton, 2011. https://eprints.soton.ac.uk/193145/.

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The dependence of crystal structure assembly on molecular changes has been studied for mono-substituted acylanilides. A library of 255 crystal structures has been investigated. 217 structures were determined during this project and 38 originated from the CSD. A subset of 64 mono-substituted acetanilides was studied in detail for crystal structure similarities using the XPac algorithm and conformational preferences were assessed. Chapter 4 presents the crystal structures and their structural similarities, whilst Chapter 5 focuses on the theoretical conformational analysis. Three amide-amide hyd
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Wyatt, Victor T. "Kinetics of the solid-liquid phase-transfer catalyzed deprotonation and N-alkylation of acetanilide." Thesis, Georgia Institute of Technology, 1998. http://hdl.handle.net/1853/27079.

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Wright, James T. Jr. "Kinetics of the deprotonation and N-alkylation of acetanilide via phase-transfer catalysis." Diss., Georgia Institute of Technology, 1996. http://hdl.handle.net/1853/27982.

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Stamper, David M. "Nucleophilic dechlorination of acetanilide herbicides by sulfide, and phylogenetic and biochemical characterization of an atrazine-mineralizing bacterium /." The Ohio State University, 2000. http://rave.ohiolink.edu/etdc/view?acc_num=osu1488196234910748.

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Mohamed, Mohamed Amer. "Synthesis, characterisation and cation coordinating properties of [N,N'-bis(acetic)-N,N'-bis(acetanilide)]ethylenediamine and its new polymeric material." Thesis, University of Surrey, 1995. http://epubs.surrey.ac.uk/843721/.

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The synthesis of [N,N'-bis(acetic)-N,N' bis(acetanilide)]ethylenediamine (EDDADA) and its characterisation by 1H and 13C NMR, IR and elemental analysis are reported. The interaction of this ligand with metal cations (Cu2+, Co2+, Ni2+, Cd2+, Hg2+ and Pb2+) in butan-1-ol was investigated spectrophotometrically and the stoichiometry (1:1) of the complexes was derived. Potentiometric titration curves of eddada with hydrochloric acid in water at 298.15 K show two inflection points corresponding to the protonation of the amino nitrogens of the ligand. The derived dissociation constants (expressed as
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Scarfe, Graeme Bryan. "The in vivo metabolism of substituted anilines and acetanilides in rat using hyphenated NMR spectroscopic techniques." Thesis, Birkbeck (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325321.

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Chen, Bing-Sheng, and 陳炳勝. "The Adaptability of Acetanilide Herbicides Degrading Bacteria in Soils." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/07740868498397585122.

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碩士<br>國立臺灣大學<br>農業化學研究所<br>93<br>The objective of this study is to confer the the adaptability of acetanilide herbicides degrading bacteria in fields and to study the the adaptability of acetanilide herbicides degrading bacteria in fields and the ability of the bacteria to degrade amide herbicide.We applied the bacteria into soil and analysised the adaptability of the bacteria and the difference between microbial community with PCR-DGGE. HPLC was used to detect the degradation of the amide herbicide.According to the result,the bacteria was well-adapted and could increase the degradation rate a
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Keshri, Puspam. "Ru (II)-Catalyzed C−H Activation: Amide-Directed 1,4-Addition of Ortho C−H Bond to Maleimides." Thesis, 2016. https://etd.iisc.ac.in/handle/2005/4927.

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Transition metal catalyzed functionalization of C-H bond to C-C bond is advantageous and atom economical. The use of directing groups is intended to overcome the challenges associated with the C-H activation such as low reactivity of C-H bond and the issue of site selectivity. Amides are well known as directing groups and found to couple with a variety of coupling partners. In this thesis, maleimide has been used as a selective coupling partner to generate conjugate addition products exclusively. The typical Heck-type oxidative coupling that occurs, when alkenes are used, is avoided by c
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Chang, Shiu Ling, and 張秀齡. "Study on adsorption, degradation and movement of acetanilide herbicides in soils." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/14119238484201554617.

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碩士<br>國立臺灣大學<br>農業化學研究所<br>89<br>Chloroacetamide herbicides are selectively, non-hormone and widely used in Taiwan. These herbicides are low toxicity to human and animals, less residue in environment and highly efficacy of control grasses. Degradation and adsortion of herbicides alachlor, butachlor, metolachlor and propachlor in three soils were studied. Movement of herbicides in soils were performed with soil columns. The BAM model and GWP model were used to estimate the relative fate and the potential of contaminating groundwater. The results indicated that the degradation rate of
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Chen, Shih-Hsien, and 陳詩弦. "The Study on Dyeability of Acetanilide Disperse Dyes in Supercritical Carbon Dioxide." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/w8xbk8.

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碩士<br>國立臺北科技大學<br>分子科學與工程系有機高分子碩士班<br>106<br>This research presents the preparation of intermediates of methyl 3-(N-methylpropionate methyl)amino-4-methoxyacetanilide with a series of diazonium salts of long-chain alkyl, halogen and nitro groups. A number of disperse dyes are filtered out after the solution undergoes coupling reactions. TLC is then used to observe the presence of impurities. If it needs purification, the structure of the dye is to confirm by H-NMR, MASS, FTIR, etc. after purification. As mentioned above, disperse dyes and polyester fibers undergo supercritical carbon dioxide d
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Books on the topic "Acetanilide"

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International Program on Chemical Safety., ed. Propachlor health and safety guide. World Health Organization for the International Programme on Chemical Safety, 1992.

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Stuart-Smith, Karen. Lidocaine: Current Concepts and Emerging Roles in Clinical Practice. Nova Science Publishers, Incorporated, 2014.

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Mallet, Christophe, and Alain Eschalier. The rediscovery of paracetamol. Edited by Paul Farquhar-Smith, Pierre Beaulieu, and Sian Jagger. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198834359.003.0004.

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The chapter describes experiments performed by Bernard B. Brodie and Julius Axelrod in an article published in 1948 and entitled ‘The fate of acetanilide in man’. This was an important breakthrough in the history of paracetamol (acetaminophen), which was synthesized in 1878 but only clinically used in 1955. We highlight how this article historically catalysed the rehabilitation (also called ‘the rediscovery’) of this popular over-the-counter painkiller. Demonstrating that paracetamol was the key active metabolite of acetanilide (an antipyretic/analgesic used at that time), and discarding the f
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Lyman F. (Lyman Frederic) B. Kebler, Francis P. (Francis Patterson) Morgan, and Philip 1862-1939 Rupp. Harmful Effects of Acetanilid, Antipyrin, and Phenacetin; Volume No. 126. Creative Media Partners, LLC, 2023.

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Propachlor (Environmental Health Criteria Series No. 147). World Health Organization, 1993.

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Book chapters on the topic "Acetanilide"

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Gooch, Jan W. "Acetanilide." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_102.

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Gooch, Jan W. "Ethyl Acetanilide." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4537.

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Gooch, Jan W. "n-Ethyl Acetanilide." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4538.

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Bigio, Irving J., Alwyn C. Scott, and Clifford T. Johnston. "Spectroscopy of the Amide-I Modes of Acetanilide." In Davydov’s Soliton Revisited. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-9948-4_27.

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Edler, J., and P. Hamm. "Femtosecond Study of Vibrational Self-Trapping in Crystalline Acetanilide." In Ultrafast Phenomena XIII. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-59319-2_182.

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Giansanti, Andrea, Alessandro Campa, Decio Levi, Orlando Ragnisco, and Alexander Tenenbaum. "Vibrational Properties and Energy Transport in Acetanilide by Molecular Dynamics." In Davydov’s Soliton Revisited. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-9948-4_34.

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Careri, Giorgio. "The Amide-I Band in Acetanilide: Physical Properties and Biological Suggestions." In Davydov’s Soliton Revisited. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-9948-4_25.

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Barthes, Mariette. "Incoherent Neutron Scattering and Infra-Red Measurements in Acetanilide and Derivatives." In Davydov’s Soliton Revisited. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-9948-4_26.

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Cruzeiro, Leonor. "The Amide I Band of Crystalline Acetanilide: Old Data Under New Light." In Quodons in Mica. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-21045-2_17.

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Hallenbeck, William H., and Kathleen M. Cunningham-Burns. "Acetanilides." In Pesticides and Human Health. Springer New York, 1985. http://dx.doi.org/10.1007/978-1-4612-5054-8_2.

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Conference papers on the topic "Acetanilide"

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Farooq, S., I. Hashmi, M. Arshad, and I. A. Qazi. "Acetanilide herbicide degradation using indigenous soil microorganisms." In SAFE 2013. WIT Press, 2013. http://dx.doi.org/10.2495/safe130611.

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Edler, J., and P. Hamm. "Femtosecond Study of Self-Trapped Vibrational Excitons in Crystalline Acetanilide." In International Conference on Ultrafast Phenomena. OSA, 2002. http://dx.doi.org/10.1364/up.2002.tua7.

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Mir, M. Amin, M. Waqar Ashraf, and Kim Andrews. "Preparation, spectral analysis of a substituted phenyl acetanilide from aniline." In FOURTH INTERNATIONAL CONFERENCE ON ADVANCES IN PHYSICAL SCIENCES AND MATERIALS: ICAPSM 2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0216052.

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Basha, A. Aathif, and F. Liakath Ali Khan. "Dielectrics relaxation studies of acrylamide and acetanilide with halogenated phenols in benzene." In PROCEEDINGS OF THE 1ST INTERNATIONAL CONFERENCE ON FRONTIER OF DIGITAL TECHNOLOGY TOWARDS A SUSTAINABLE SOCIETY. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0113412.

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