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4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde

The title compound, C(15)H(22)O(3), crystallizes with two independent mol­ecules in the asymmetric unit. In each mol­ecule, one hy­droxy group (at position 2) is involved in an intra­molecular O—H⋯O hydrogen bond, and another one (at position 3) exhibits bifurcated hydrogen-bonding being involved in...

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Autores principales: Arsenyev, Max, Baranov, Eugene, Chesnokov, Sergey, Abakumov, Gleb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790425/
https://www.ncbi.nlm.nih.gov/pubmed/24098244
http://dx.doi.org/10.1107/S1600536813025488
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author Arsenyev, Max
Baranov, Eugene
Chesnokov, Sergey
Abakumov, Gleb
author_facet Arsenyev, Max
Baranov, Eugene
Chesnokov, Sergey
Abakumov, Gleb
author_sort Arsenyev, Max
collection PubMed
description The title compound, C(15)H(22)O(3), crystallizes with two independent mol­ecules in the asymmetric unit. In each mol­ecule, one hy­droxy group (at position 2) is involved in an intra­molecular O—H⋯O hydrogen bond, and another one (at position 3) exhibits bifurcated hydrogen-bonding being involved in intra- and inter­molecular O—H⋯O inter­actions. In the crystal, O—H⋯O hydrogen bonds link alternating independent mol­ecules into chains running along [010].
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spelling pubmed-37904252013-10-04 4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde Arsenyev, Max Baranov, Eugene Chesnokov, Sergey Abakumov, Gleb Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(22)O(3), crystallizes with two independent mol­ecules in the asymmetric unit. In each mol­ecule, one hy­droxy group (at position 2) is involved in an intra­molecular O—H⋯O hydrogen bond, and another one (at position 3) exhibits bifurcated hydrogen-bonding being involved in intra- and inter­molecular O—H⋯O inter­actions. In the crystal, O—H⋯O hydrogen bonds link alternating independent mol­ecules into chains running along [010]. International Union of Crystallography 2013-09-18 /pmc/articles/PMC3790425/ /pubmed/24098244 http://dx.doi.org/10.1107/S1600536813025488 Text en © Arsenyev et al. 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
Arsenyev, Max
Baranov, Eugene
Chesnokov, Sergey
Abakumov, Gleb
4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde
title 4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde
title_full 4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde
title_fullStr 4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde
title_full_unstemmed 4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde
title_short 4,6-Di-tert-butyl-2,3-di­hydroxy­benzalde­hyde
title_sort 4,6-di-tert-butyl-2,3-di­hydroxy­benzalde­hyde
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790425/
https://www.ncbi.nlm.nih.gov/pubmed/24098244
http://dx.doi.org/10.1107/S1600536813025488
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