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trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid
The title compound, C(15)H(20)O(5)S, is an intermediate in the synthesis of a new type of poly(amidoamine) (PAMAM) dendrimer. The cyclohexane ring exhibits a chair conformation, with C—C bond lengths in the range 1.518 (3)–1.531 (3) Å and C—C—C angles in the range 110.45 (19)–112.09 (19)°; these...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960345/ https://www.ncbi.nlm.nih.gov/pubmed/21201433 http://dx.doi.org/10.1107/S1600536807068572 |
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author | Qi, Qing-Rong Huang, Wen-Cai Zheng, Hu |
author_facet | Qi, Qing-Rong Huang, Wen-Cai Zheng, Hu |
author_sort | Qi, Qing-Rong |
collection | PubMed |
description | The title compound, C(15)H(20)O(5)S, is an intermediate in the synthesis of a new type of poly(amidoamine) (PAMAM) dendrimer. The cyclohexane ring exhibits a chair conformation, with C—C bond lengths in the range 1.518 (3)–1.531 (3) Å and C—C—C angles in the range 110.45 (19)–112.09 (19)°; these agree well with the values in other cyclohexane derivatives described in the literature. In the crystal structure, adjacent molecules are linked by O—H⋯·O hydrogen bonds. The H atoms of the methyl group are disordered equally over two positions. |
format | Text |
id | pubmed-2960345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29603452010-12-30 trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid Qi, Qing-Rong Huang, Wen-Cai Zheng, Hu Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(20)O(5)S, is an intermediate in the synthesis of a new type of poly(amidoamine) (PAMAM) dendrimer. The cyclohexane ring exhibits a chair conformation, with C—C bond lengths in the range 1.518 (3)–1.531 (3) Å and C—C—C angles in the range 110.45 (19)–112.09 (19)°; these agree well with the values in other cyclohexane derivatives described in the literature. In the crystal structure, adjacent molecules are linked by O—H⋯·O hydrogen bonds. The H atoms of the methyl group are disordered equally over two positions. International Union of Crystallography 2008-01-09 /pmc/articles/PMC2960345/ /pubmed/21201433 http://dx.doi.org/10.1107/S1600536807068572 Text en © Qi et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Qi, Qing-Rong Huang, Wen-Cai Zheng, Hu trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid |
title |
trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid |
title_full |
trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid |
title_fullStr |
trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid |
title_full_unstemmed |
trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid |
title_short |
trans-4-(Tosyloxymethyl)cyclohexanecarboxylic acid |
title_sort | trans-4-(tosyloxymethyl)cyclohexanecarboxylic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960345/ https://www.ncbi.nlm.nih.gov/pubmed/21201433 http://dx.doi.org/10.1107/S1600536807068572 |
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