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Methyl 4-(trimethylsilylethynyl)benzoate
The title compound, C(13)H(16)O(2)Si, was synthesized as a precursor for ethynylarene derivatives and crystallized from hexane. In the crystal structure, molecules are linked by weak C—H⋯O hydrogen bonds to form chains that pack in layers in a herringbone fashion.
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961551/ https://www.ncbi.nlm.nih.gov/pubmed/21202696 http://dx.doi.org/10.1107/S1600536808008192 |
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author | Potts, Storm Das, Dinabandhu Bredenkamp, Martin W. |
author_facet | Potts, Storm Das, Dinabandhu Bredenkamp, Martin W. |
author_sort | Potts, Storm |
collection | PubMed |
description | The title compound, C(13)H(16)O(2)Si, was synthesized as a precursor for ethynylarene derivatives and crystallized from hexane. In the crystal structure, molecules are linked by weak C—H⋯O hydrogen bonds to form chains that pack in layers in a herringbone fashion. |
format | Text |
id | pubmed-2961551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29615512010-12-30 Methyl 4-(trimethylsilylethynyl)benzoate Potts, Storm Das, Dinabandhu Bredenkamp, Martin W. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(16)O(2)Si, was synthesized as a precursor for ethynylarene derivatives and crystallized from hexane. In the crystal structure, molecules are linked by weak C—H⋯O hydrogen bonds to form chains that pack in layers in a herringbone fashion. International Union of Crystallography 2008-05-03 /pmc/articles/PMC2961551/ /pubmed/21202696 http://dx.doi.org/10.1107/S1600536808008192 Text en © Potts 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 Potts, Storm Das, Dinabandhu Bredenkamp, Martin W. Methyl 4-(trimethylsilylethynyl)benzoate |
title | Methyl 4-(trimethylsilylethynyl)benzoate |
title_full | Methyl 4-(trimethylsilylethynyl)benzoate |
title_fullStr | Methyl 4-(trimethylsilylethynyl)benzoate |
title_full_unstemmed | Methyl 4-(trimethylsilylethynyl)benzoate |
title_short | Methyl 4-(trimethylsilylethynyl)benzoate |
title_sort | methyl 4-(trimethylsilylethynyl)benzoate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961551/ https://www.ncbi.nlm.nih.gov/pubmed/21202696 http://dx.doi.org/10.1107/S1600536808008192 |
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