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(E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid
The title compound, C(12)H(11)NO(4)S, is a Schiff base derived from the condensation reaction of equimolar quantities of sulfamide and furfural. The molecule has a trans configuration with respect to the imine C=N double bond. The N atom is involved in an intermolecular O—H—N hydrogen bond....
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960525/ https://www.ncbi.nlm.nih.gov/pubmed/21201768 http://dx.doi.org/10.1107/S1600536808026275 |
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author | Suo, Jianlan |
author_facet | Suo, Jianlan |
author_sort | Suo, Jianlan |
collection | PubMed |
description | The title compound, C(12)H(11)NO(4)S, is a Schiff base derived from the condensation reaction of equimolar quantities of sulfamide and furfural. The molecule has a trans configuration with respect to the imine C=N double bond. The N atom is involved in an intermolecular O—H—N hydrogen bond. |
format | Text |
id | pubmed-2960525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29605252010-12-30 (E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid Suo, Jianlan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(11)NO(4)S, is a Schiff base derived from the condensation reaction of equimolar quantities of sulfamide and furfural. The molecule has a trans configuration with respect to the imine C=N double bond. The N atom is involved in an intermolecular O—H—N hydrogen bond. International Union of Crystallography 2008-08-20 /pmc/articles/PMC2960525/ /pubmed/21201768 http://dx.doi.org/10.1107/S1600536808026275 Text en © Jianlan Suo 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 Suo, Jianlan (E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid |
title | (E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid |
title_full | (E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid |
title_fullStr | (E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid |
title_full_unstemmed | (E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid |
title_short | (E)-4-[(5-Methyl-2-furyl)methyleneamino]benzenesulfonic acid |
title_sort | (e)-4-[(5-methyl-2-furyl)methyleneamino]benzenesulfonic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960525/ https://www.ncbi.nlm.nih.gov/pubmed/21201768 http://dx.doi.org/10.1107/S1600536808026275 |
work_keys_str_mv | AT suojianlan e45methyl2furylmethyleneaminobenzenesulfonicacid |