Relevant bibliographies by topics / 3-Chloro-4-Fluoroaniline

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic '3-Chloro-4-Fluoroaniline'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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

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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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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Dissertations / Theses on the topic "3-Chloro-4-Fluoroaniline"

1

Hsuan, Huang Yi, and 黃苡瑄. "4-Chloro-3-fluoroaniline and 4-Chloro-3-fluoroanisole studied by resonant two-photon ionization and mass-analyzed threshold ionization spectroscopy." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/14648068725536898218.

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碩士<br>國立臺灣師範大學<br>化學系<br>102<br>We applied the resonant two-photon ionization and mass-analyzed threshold ionization techniques to record the vibronic and cation spectra of 4-chloro-3-fluoroaniline and 4-chloro-3-fluoroanisole to investigate their molecular properties. The excitation energy of the S1 ← S0 transition (E1) and the adiabatic ionization energy (IE) of 4-chloro-3-fluoroaniline are found to be 33 242 and 63 868 cm-1, respectively. Comparing these data with those of 4-chloroaniline, 3-fluoroaniline, and aniline, we find an additivity rule associated with the E1 and IE. This implies t
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2

Lo, Ko-Wei, and 駱可薇. "3-Chloro-4-fluoroaniline studied by resonant two-photon ionization and mass analyzed threshold ionization spectroscopy." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/10207622064648487951.

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碩士<br>國立臺灣師範大學<br>化學系<br>101<br>We applied the resonant two-photon ionization and mass-analyzed threshold ionization spectroscopic techniques to record the vibronic and cation spectra of 3-chloro-4-fluoroaniline (3C4FA). Within our experimental detection limit, the measured values are the same for both of the 35Cl and 37Cl isotopologues of 3C4FA. The band origin of the S1 ← S0 electronic transition (E1) was found to be 32 348 ± 2 cm-1, and the adiabatic ionization energy (IE) was determined to be 63 872 ± 5 cm-1. Most of the observed active modes of 3C4FA in the electronically excited S1 and c
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Journal articles
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