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4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid

The synthesis and spectroscopic characterization of the glutaric acid-amide derivative, 2,4-Cl2C6H3N(H)C(=O)(CH2)3C(=O)OH (1), are described. The X-ray crystal structure determination of (1) shows the backbone of the molecule to be kinked about the methylene-C–N(amide) bond as seen in the C(p)–N–C(m...

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Main Authors: Hanifa, B., Sirajuddin, M., Ullah, Z., Sumera, M., Lee, See Mun *, Lo, Kong Mun *, Tiekink, Edward R. T. *
Format: Article
Language:English
Published: MDPI 2021
Subjects:
QD Chemistry
Online Access:http://eprints.sunway.edu.my/1780/1/Tiekink%20molbank-2021-m1227.pdf
http://eprints.sunway.edu.my/1780/
https://doi.org/10.3390/M1227
https://doi.org/10.3390/M1227
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spelling my.sunway.eprints.17802021-08-27T06:14:24Z http://eprints.sunway.edu.my/1780/ 4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid Hanifa, B. Sirajuddin, M. Ullah, Z. Sumera, M. Lee, See Mun * Lo, Kong Mun * Tiekink, Edward R. T. * QD Chemistry The synthesis and spectroscopic characterization of the glutaric acid-amide derivative, 2,4-Cl2C6H3N(H)C(=O)(CH2)3C(=O)OH (1), are described. The X-ray crystal structure determination of (1) shows the backbone of the molecule to be kinked about the methylene-C–N(amide) bond as seen in the C(p)–N–C(m)–C(m) torsion angle of −157.0(2)°; m = methylene and p = phenyl. An additional twist in the molecule is noted between the amide and phenyl groups as reflected in the C(m)–N–C(p)–C(p) torsion angle of 138.2(2)°. The most prominent feature of the molecular packing is the formation of supramolecular tapes assembled through carboxylic acid-O–H…O(carbonyl) and amide-N–H…O(amide) hydrogen bonding. MDPI 2021-06 Article PeerReviewed text en cc_by_nc_4 http://eprints.sunway.edu.my/1780/1/Tiekink%20molbank-2021-m1227.pdf Hanifa, B. and Sirajuddin, M. and Ullah, Z. and Sumera, M. and Lee, See Mun * and Lo, Kong Mun * and Tiekink, Edward R. T. * (2021) 4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid. Molbank (M1227). ISSN 1422-8599 https://doi.org/10.3390/M1227 https://doi.org/10.3390/M1227
institution Sunway University
building Sunway Campus Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Sunway University
content_source Sunway Institutional Repository
url_provider http://eprints.sunway.edu.my/
language English
topic QD Chemistry
spellingShingle QD Chemistry
Hanifa, B.
Sirajuddin, M.
Ullah, Z.
Sumera, M.
Lee, See Mun *
Lo, Kong Mun *
Tiekink, Edward R. T. *
4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid
description The synthesis and spectroscopic characterization of the glutaric acid-amide derivative, 2,4-Cl2C6H3N(H)C(=O)(CH2)3C(=O)OH (1), are described. The X-ray crystal structure determination of (1) shows the backbone of the molecule to be kinked about the methylene-C–N(amide) bond as seen in the C(p)–N–C(m)–C(m) torsion angle of −157.0(2)°; m = methylene and p = phenyl. An additional twist in the molecule is noted between the amide and phenyl groups as reflected in the C(m)–N–C(p)–C(p) torsion angle of 138.2(2)°. The most prominent feature of the molecular packing is the formation of supramolecular tapes assembled through carboxylic acid-O–H…O(carbonyl) and amide-N–H…O(amide) hydrogen bonding.
format Article
author Hanifa, B.
Sirajuddin, M.
Ullah, Z.
Sumera, M.
Lee, See Mun *
Lo, Kong Mun *
Tiekink, Edward R. T. *
author_facet Hanifa, B.
Sirajuddin, M.
Ullah, Z.
Sumera, M.
Lee, See Mun *
Lo, Kong Mun *
Tiekink, Edward R. T. *
author_sort Hanifa, B.
title 4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid
title_short 4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid
title_full 4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid
title_fullStr 4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid
title_full_unstemmed 4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid
title_sort 4-[(2,4-dichlorophenyl)carbamoyl]butanoic acid
publisher MDPI
publishDate 2021
url http://eprints.sunway.edu.my/1780/1/Tiekink%20molbank-2021-m1227.pdf
http://eprints.sunway.edu.my/1780/
https://doi.org/10.3390/M1227
https://doi.org/10.3390/M1227
_version_ 1709671213867991040
score 13.211869

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