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Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate
In the title compound, C(7)H(10)N(2)O(2), the dimethylamino group is twisted slightly relative to the acrylate fragment, forming a dihedral angle of 11.6 (1)°. In the crystal, molecules are linked via pairs of bifurcated C—H/H⋯O hydrogen bonds, forming inversion dimers, which are further connected...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515226/ https://www.ncbi.nlm.nih.gov/pubmed/23284446 http://dx.doi.org/10.1107/S1600536812042304 |
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author | Kant, Rajni Gupta, Vivek K. Kapoor, Kamini Patil, D. R. Salunkhe, D. K. Deshmukh, Madhukar B. |
author_facet | Kant, Rajni Gupta, Vivek K. Kapoor, Kamini Patil, D. R. Salunkhe, D. K. Deshmukh, Madhukar B. |
author_sort | Kant, Rajni |
collection | PubMed |
description | In the title compound, C(7)H(10)N(2)O(2), the dimethylamino group is twisted slightly relative to the acrylate fragment, forming a dihedral angle of 11.6 (1)°. In the crystal, molecules are linked via pairs of bifurcated C—H/H⋯O hydrogen bonds, forming inversion dimers, which are further connected by C—H⋯N hydrogen bonds into chains along the a-axis direction. |
format | Online Article Text |
id | pubmed-3515226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35152262013-01-02 Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate Kant, Rajni Gupta, Vivek K. Kapoor, Kamini Patil, D. R. Salunkhe, D. K. Deshmukh, Madhukar B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(7)H(10)N(2)O(2), the dimethylamino group is twisted slightly relative to the acrylate fragment, forming a dihedral angle of 11.6 (1)°. In the crystal, molecules are linked via pairs of bifurcated C—H/H⋯O hydrogen bonds, forming inversion dimers, which are further connected by C—H⋯N hydrogen bonds into chains along the a-axis direction. International Union of Crystallography 2012-10-13 /pmc/articles/PMC3515226/ /pubmed/23284446 http://dx.doi.org/10.1107/S1600536812042304 Text en © Kant et al. 2012 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 Kant, Rajni Gupta, Vivek K. Kapoor, Kamini Patil, D. R. Salunkhe, D. K. Deshmukh, Madhukar B. Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate |
title | Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate |
title_full | Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate |
title_fullStr | Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate |
title_full_unstemmed | Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate |
title_short | Methyl (2E)-2-cyano-3-(dimethylamino)prop-2-enoate |
title_sort | methyl (2e)-2-cyano-3-(dimethylamino)prop-2-enoate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515226/ https://www.ncbi.nlm.nih.gov/pubmed/23284446 http://dx.doi.org/10.1107/S1600536812042304 |
work_keys_str_mv | AT kantrajni methyl2e2cyano3dimethylaminoprop2enoate AT guptavivekk methyl2e2cyano3dimethylaminoprop2enoate AT kapoorkamini methyl2e2cyano3dimethylaminoprop2enoate AT patildr methyl2e2cyano3dimethylaminoprop2enoate AT salunkhedk methyl2e2cyano3dimethylaminoprop2enoate AT deshmukhmadhukarb methyl2e2cyano3dimethylaminoprop2enoate |