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Journal articles on the topic '3-Chloro-4-Fluoroaniline'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Arjuna Gowda, K. V., M. K. Kokila, Puttaraja, M. V. Kulkarni, and N. C. Shivaprakash. "(E)-N-Benzylidene-3-chloro-4-fluoroaniline." Acta Crystallographica Section C Crystal Structure Communications 56, no. 10 (2000): e481-e482. http://dx.doi.org/10.1107/s0108270100012166.

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2

Jasinski, Jerry P., Albert E. Pek, C. S. Chidan Kumar, H. S. Yathirajan, and Suresh Kumar. "N-[(2-Chloro-3-quinolyl)methyl]-4-fluoroaniline." Acta Crystallographica Section E Structure Reports Online 66, no. 10 (2010): o2548—o2549. http://dx.doi.org/10.1107/s1600536810036056.

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3

Betz, R. "Crystal and molecular structure of 2,6-dibromo-3-chloro-4-fluoroaniline." Crystallography Reports 60, no. 7 (2015): 1049–52. http://dx.doi.org/10.1134/s1063774515070056.

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4

Pang, Yan, and Zhong Wei Wang. "Analysis on Health Risk of Extractives of Cinnamomum camphora by Py-GC-MS." Key Engineering Materials 480-481 (June 2011): 242–45. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.242.

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In order to evaluate its potential health risk to food, Py-GC/MS was used to analyze the high-grade resource recovery of benzene/ethanol extractives of the Cinnamomum camphora wood. Relative content of each component was determined by area normalization. The main constituents were hexadecanoic acid, oleic Acid, octadecanoic acid, 4-chloro-2-fluoroaniline, cyclohexane, 1,1-dimethyl-, 7-heptadecene, 17-chloro-, brucine, ergosta-4,6,22-trien-3.beta.-ol, etc. So the benzene/ethanol extractives of Cinnamomum camphora could be used as materials of biomedicine.

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5

Rajuna Gowda, K. V., M. K. Kokila, Puttaraja, M. V. Kulkarni, and N. C. Shivaprakash. "Crystal and molecular structure of N-(p-nitrobenzylidene)-3-chloro-4-fluoroaniline." Pramana 55, no. 3 (2000): 441–46. http://dx.doi.org/10.1007/s12043-000-0074-5.

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6

Mishra, A. P., A. Tiwari, S. K. Gupta, and Rajendra Jain. "Synthesis, Spectral and Antimicrobial Studies of Some Co(II), Ni(II) and Cu(II) Complexes Containing 2-Thiophenecarboxaldehyde Moiety." E-Journal of Chemistry 9, no. 3 (2012): 1113–21. http://dx.doi.org/10.1155/2012/585827.

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Some new Schiff base metal complexes of Co(II), Ni(II) and Cu(II) derived from 3-chloro-4-fluoroaniline (HL1) and 4-fluoroaniline (HL2) with 2-thiophenecarboxaldehyde have been synthesized and characterized by elemental analysis, FT-IR, FAB-mass, molar conductance, electronic spectra, ESR and magnetic susceptibility. The complexes exhibit coordination number 4 or 6. The complexes are colored and stable in air. Analytical data revealed that all the complexes exhibited 1:2 (metal: ligand) ratio. FAB-mass data show degradation pattern of the complexes. The Schiff base and metal complexes show a g

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7

Aesha F SH Abdassalam, Aesha F. SH Abdassalam, Semih Kurban Semih Kurban, and Nahide Gulsah Deniz and Cigdem Sayil Nahide Gulsah Deniz and Cigdem Sayil. "Synthesis and Characterization of New Naphtho- and Tetracyclic Diazaquinone Derivatives." Journal of the chemical society of pakistan 41, no. 5 (2019): 834. http://dx.doi.org/10.52568/000805/jcsp/41.05.2019.

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In this study, new 1,4-naphtho- and 5-nitro-1,4-naphtho derivatives containing N- and N,N-substituted groups which has not been reported yet, have been synthesized from 2,3-dichloronaphthalene-1,4-diones (1,9). Compounds of 2-choloro-3-((2,4,6-triflorophenyl)amino)naphthalene-1,4-dione (3) and 2-chloro-3-((4-florophenyl)amino)naphtalene-1,4-dione (7) were obtained by reactions of 2,3-dichloronaphthalene-1,4-dione 1 with 4-fluoroaniline (6) and 2,4,6-trifloroaniline (2), respectively involving a Michael addition. We reported the cyclization reactions of compounds 1 to benzo[g]pirido[3,2-b]quino

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8

Zhu, Shengdong, Yuanxin Wu, Ziniu Yu, et al. "One-Pot Synthesis of Norfloxacin Ethyl Ester from 3-Chloro-4- Fluoroaniline in Ionic Liquid." Letters in Organic Chemistry 5, no. 1 (2008): 1–2. http://dx.doi.org/10.2174/157017808783330126.

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9

Wang, Weilai, Xinting Guo, Zekun Liu, et al. "Micro-nano H2 bubbles enhanced hydrodehalogenation of 3-chloro-4-fluoroaniline: Mass transfer and action mechanism." Chemosphere 363 (September 2024): 142816. http://dx.doi.org/10.1016/j.chemosphere.2024.142816.

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10

Lo, Ko Wei, and Wen Bih Tzeng. "3-Chloro-4-fluoroaniline studied by resonant two-photon ionization and mass-analyzed threshold ionization spectroscopy." Journal of Molecular Spectroscopy 288 (June 2013): 1–6. http://dx.doi.org/10.1016/j.jms.2013.03.005.

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11

Huang, Yi Hsuan, Wei Chih Huang, and Wen Bih Tzeng. "4-Chloro-3-fluoroaniline studied by resonant two-photon ionization and mass-analyzed threshold ionization spectroscopy." Chemical Physics Letters 595-596 (March 2014): 73–76. http://dx.doi.org/10.1016/j.cplett.2014.01.038.

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12

Pirgal, Dimple. "Microwave assisted synthesis of 3-substituted aryl aminochloro flouroquinoline derivatives for antimicrobial activities." Journal of medical pharmaceutical and allied sciences 11, no. 6 (2022): 5461–68. http://dx.doi.org/10.55522/jmpas.v11i6.3968.

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Quinoline derivatives found to possess various activities such as antimicrobial, anti-tubercular, antifungal etc. 2,7-dichloro-6- fluoroquinoline-3-carbaldehyde was synthesized by treating 3-chloro-4-fluoroaniline with acetic anhydride, the intermediate (substituted acetanilide) obtained was further treated under microwave with dimethyl formamide /phosphorus oxychloride to get the desired product. Derivatives of 2,7- dichloro-6-fluoroquinoline-3- carbaldehyde [R-02] to [R-10] were synthesized by treating it with different anilines, oxindole and rhodanine. Synthesized derivatives were character

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13

Witwit, Israa N., Husham M. Mubark, Zahraa Y. Motaweq, and Mohauman M. Al Rufaie. "SYNTHESIS, BACTERIAL INHIBITION, AND COORDINATION BEHAVIOR STUDY OF NEW AZOIMIDAZOLE LIGAND WITH SOME OF FIRST SERIES TRANSITION IONS." ACTA CHEMICA IASI 31, no. 2 (2024): 129–46. http://dx.doi.org/10.47743/achi-2023-2-0009.

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Coupling reaction between the diazonium salt of 3-chloro-4- fluoroaniline and 4-methyl imidazole used to create new Azoimidazole compound (4MCFD). Solid complexes of this ligand and series of transition metal ion were synthesized. The complexes and ligand were characterized by Mass Spectroscopy, 1H-NMR,13C-NMR, FT-IR, UV-Vis, Elemental Analysis, Molar Conductivity, and their inhibition ability against E. coli, P. aeruginosa, K. pneumonia, and S. aureus bacteria studied, according to the common chemical characterization methods. The values of stability constants were also calculated and showed

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14

Eadsforth, C. V., P. C. Coveney, and W. H. A. Sjoe. "An Improved Analytical Method, Based on HPLC with Electrochemical Detection, for Monitoring Exposure to 3-Chloro-4-fluoroaniline." Journal of Analytical Toxicology 12, no. 6 (1988): 330–33. http://dx.doi.org/10.1093/jat/12.6.330.

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15

Eşme, A., and S. G. Sağdınç. "Quantum Chemical Calculations of the Spectroscopic Properties and Nonlinear Optical Activity of 2,6-Dibromo-3-Chloro-4-Fluoroaniline." Journal of Applied Spectroscopy 84, no. 6 (2018): 1098–107. http://dx.doi.org/10.1007/s10812-018-0594-8.

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16

A., P. Mishra, Sharma Neha, and Jain Rajendra. "Synthesis and structure of some novel Schiff base complexes with CuII and NiII." Journal of Indian Chemical Society Vol. 88, Sep 2011 (2011): 1429–34. https://doi.org/10.5281/zenodo.5788979.

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Bioinorganic Research Laboratories, Department of Chemistry, Dr. H. S. Gour University, Sagar-470 003, Madhya Pradesh, India <em>E-mail</em> : apm19@rediffmail.com <em>Manuscript received 15 June 2010, revised 31 January 2011, accepted 02 February 2011</em> The chemistry of metal complexes with tailor made Schiff base ligands and their applications, have aroused considerable interest mainly because of preparative accessibility, diverse reactivity and structural variability. Complexes of Nill and Cu11 with the Schiff bases viz. 3,4-dichloroaniline with 2-furfuraldehyde/4-dimethylaminobenza

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17

Boogaard, Pieter J., Gerard D. J. Beulink, and Nico J. van Sittert. "Biological Monitoring of Exposure to 3-Chloro-4-Fluoroaniline by Determination of a Urinary Metabolite and a Hemoglobin Adduct." Environmental Health Perspectives 102 (October 1994): 23. http://dx.doi.org/10.2307/3432146.

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18

Boogaard, P. J., G. D. Beulink, and N. J. van Sittert. "Biological monitoring of exposure to 3-chloro-4-fluoroaniline by determination of a urinary metabolite and a hemoglobin adduct." Environmental Health Perspectives 102, suppl 6 (1994): 23–25. http://dx.doi.org/10.1289/ehp.94102s623.

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19

Duckett, C. J., J. C. Lindon, H. Walker, F. Abou-Shakra, I. D. Wilson, and J. K. Nicholson. "Metabolism of 3-chloro-4-fluoroaniline in rat using [14C]-radiolabelling,19F-NMR spectroscopy, HPLC-MS/MS, HPLC-ICPMS and HPLC-NMR." Xenobiotica 36, no. 1 (2006): 59–77. http://dx.doi.org/10.1080/00498250500489927.

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20

Gowda, K. V. Arjuna, V. Prakash, M. K. Kokila, Puttaraja, M. V. Kulkarni, and N. C. Shivaprakash. "Crystal and molecular structure of N-(p-chlorobenzylidene)-3-chloro-4-fluoroaniline." Zeitschrift für Kristallographie - Crystalline Materials 214, no. 12 (1999). http://dx.doi.org/10.1524/zkri.1999.214.12.857.

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21

Zhu, Shengdong, Yuanxin Wu, Ziniu Yu, et al. "ChemInform Abstract: One-Pot Synthesis of Norfloxacin Ethyl Ester from 3-Chloro-4-fluoroaniline in Ionic Liquid." ChemInform 39, no. 20 (2008). http://dx.doi.org/10.1002/chin.200820208.

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22

Trivedi, Mahendra Kumar, Rama Mohan Tallapragada, Alice Branton, et al. "Biofield Energy Treatment: A Potential Strategy for Modulating Physical, Thermal and Spectral Properties of 3-Chloro-4-fluoroaniline." Journal of Thermodynamics & Catalysis 6, no. 3 (2015). https://doi.org/10.4172/2157-7544.1000151.

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3-Chloro-4-fluoroaniline (CFA) is used as an intermediate for the synthesis of pharmaceutical compounds. The objective of this study was to investigate the influence of biofield energy treatment on the physical, thermal and spectral properties of CFA. The study was performed in two groups (control and treated). The control group remained as untreated, and the treated group received Mr. Trivedi’s biofield energy treatment. The control and treated CFA samples were further characterized by x-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), fo

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23

Trivedi, Mahendra Kumar, Rama Mohan Tallapragada, Alice Branton, et al. "Biofield Energy Treatment: A Potential Strategy for Modulating Physical, Thermal and Spectral Properties of 3-Chloro-4-fluoroaniline." Journal of Thermodynamics & Catalysis 6, no. 3 (2015). https://doi.org/10.5281/zenodo.168530.

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3-Chloro-4-fluoroaniline (CFA) is used as an intermediate for the synthesis of pharmaceutical compounds. The objective of this study was to investigate the influence of biofield energy treatment on the physical, thermal and spectral properties of CFA. The study was performed in two groups (control and treated). The control group remained as untreated, and the treated group received Mr. Trivedi’s biofield energy treatment. The control and treated CFA samples were further characterized by x-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), fo

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24

Kumar Trivedi, Mahendra, and Rama Mohan Tallapragada. "Biofield Energy Treatment: A Potential Strategy for Modulating Physical, Thermal and Spectral Properties of 3-Chloro-4-fluoroaniline." Journal of Thermodynamics & Catalysis 06, no. 03 (2015). http://dx.doi.org/10.4172/2157-7544.1000151.

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25

Trivedi, Mahendra, Alice Branton, Dahryn Trivedi, and Gopal Nayak. "Biofield Energy Treatment: A Potential Strategy for Modulating Physical, Thermal and Spectral Properties of 3-Chloro-4-fluoroaniline." http://www.omicsonline.org/, October 15, 2015. https://doi.org/10.5281/zenodo.813579.

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3-Chloro-4-fluoroaniline (CFA) is used as an intermediate for the synthesis of pharmaceutical compounds. The objective of this study was to investigate the influence of biofield energy treatment on the physical, thermal and spectral properties of CFA. The study was performed in two groups (control and treated). The control group remained as untreated, and the treated group received Mr. Trivedi's biofield energy treatment. The control and treated CFA samples were further characterized by x-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), fourier

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26

Oladipo, Segun D., Robert C. Luckay, Samuel O. Olalekan, et al. "Probing the Inhibitory Potential of Halogenated Symmetrical Formamidine Against MAO‐A and MAO‐B: Structural Elucidation, Molecular Dynamic Simulation and DFT Computational Studies." Chemistry & Biodiversity, June 13, 2025. https://doi.org/10.1002/cbdv.202500886.

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ABSTRACTA halogenated symmetrical formamidine, N,N′‐bis(3‐chloro‐4‐fluorophenyl)formamidine (FCF) was synthesized by the condensation reaction between triethyl orthoformate and 3‐chloro‐4‐fluoroaniline in 1:2 ratio. The compound FCF was characterized by FT‐IR, mass, NMR (1H and 13C) spectroscopic techniques and the purity was confirmed by elemental analysis. Crystal structural elucidation of FCF showed that it conformed to an E‐anti‐molecular isomer. In the crystal packing system of FCF, there exists N─H⋯N hydrogen bonding intermolecular interactions between the azomethine nitrogen (N‐azomethi

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