[(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol

The title compound, C(5)H(8)Cl(2)O(2), represents a meso isomer crystallizing in a chiral space group with two mol­ecules per asymmetric unit. The mol­ecules form helical associates with a pitch of 6.31 Å along the a axis via O—H⋯O hydrogen bonds. The overall three-dimesional supra­molecular archite...

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Autor principal: Kailani, Mohammed H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569760/
https://www.ncbi.nlm.nih.gov/pubmed/23424506
http://dx.doi.org/10.1107/S1600536813000366
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author Kailani, Mohammed H.
author_facet Kailani, Mohammed H.
author_sort Kailani, Mohammed H.
collection PubMed
description The title compound, C(5)H(8)Cl(2)O(2), represents a meso isomer crystallizing in a chiral space group with two mol­ecules per asymmetric unit. The mol­ecules form helical associates with a pitch of 6.31 Å along the a axis via O—H⋯O hydrogen bonds. The overall three-dimesional supra­molecular architecture is stabilized by C—Cl⋯O halogen bonding, with a Cl⋯O separation of 3.139 (3) Å and a C—Cl⋯O angle of 162.5 (2)°.
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spelling pubmed-35697602013-02-19 [(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol Kailani, Mohammed H. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(5)H(8)Cl(2)O(2), represents a meso isomer crystallizing in a chiral space group with two mol­ecules per asymmetric unit. The mol­ecules form helical associates with a pitch of 6.31 Å along the a axis via O—H⋯O hydrogen bonds. The overall three-dimesional supra­molecular architecture is stabilized by C—Cl⋯O halogen bonding, with a Cl⋯O separation of 3.139 (3) Å and a C—Cl⋯O angle of 162.5 (2)°. International Union of Crystallography 2013-01-12 /pmc/articles/PMC3569760/ /pubmed/23424506 http://dx.doi.org/10.1107/S1600536813000366 Text en © Mohammed H. Kailani 2013 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
Kailani, Mohammed H.
[(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol
title [(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol
title_full [(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol
title_fullStr [(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol
title_full_unstemmed [(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol
title_short [(1R,3S)-2,2-Dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol
title_sort [(1r,3s)-2,2-dichloro-3-(hy­droxy­meth­yl)cyclo­prop­yl]methanol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569760/
https://www.ncbi.nlm.nih.gov/pubmed/23424506
http://dx.doi.org/10.1107/S1600536813000366
work_keys_str_mv AT kailanimohammedh 1r3s22dichloro3hydroxymethylcyclopropylmethanol

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