4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate

In the title compound, C(12)H(15)NO(7)·0.5H(2)O, there are two independent mol­ecules in the asymmetric unit, together with one water molecule. The pyran­oside rings each have close to a (1) C (4) chair conformation and the nitro groups are almost coplanar with the benzene rings. The water mol­ecule...

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Autores principales: Peltier, Pauline, Daniellou, Richard, Roisnel, Thierry, Nugier-Chauvin, Caroline, Ferrières, Vincent
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960228/
https://www.ncbi.nlm.nih.gov/pubmed/21201409
http://dx.doi.org/10.1107/S1600536807068195
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author Peltier, Pauline
Daniellou, Richard
Roisnel, Thierry
Nugier-Chauvin, Caroline
Ferrières, Vincent
author_facet Peltier, Pauline
Daniellou, Richard
Roisnel, Thierry
Nugier-Chauvin, Caroline
Ferrières, Vincent
author_sort Peltier, Pauline
collection PubMed
description In the title compound, C(12)H(15)NO(7)·0.5H(2)O, there are two independent mol­ecules in the asymmetric unit, together with one water molecule. The pyran­oside rings each have close to a (1) C (4) chair conformation and the nitro groups are almost coplanar with the benzene rings. The water mol­ecule links the two independent mol­ecules through O—H⋯O hydrogen bonds. All the hydroxyl groups are involved in hydrogen-bond inter­actions, giving rise to a three-dimensional network.
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spelling pubmed-29602282010-12-30 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate Peltier, Pauline Daniellou, Richard Roisnel, Thierry Nugier-Chauvin, Caroline Ferrières, Vincent Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(15)NO(7)·0.5H(2)O, there are two independent mol­ecules in the asymmetric unit, together with one water molecule. The pyran­oside rings each have close to a (1) C (4) chair conformation and the nitro groups are almost coplanar with the benzene rings. The water mol­ecule links the two independent mol­ecules through O—H⋯O hydrogen bonds. All the hydroxyl groups are involved in hydrogen-bond inter­actions, giving rise to a three-dimensional network. International Union of Crystallography 2008-01-09 /pmc/articles/PMC2960228/ /pubmed/21201409 http://dx.doi.org/10.1107/S1600536807068195 Text en © International Union of Crystallography 2008 http://journals.iucr.org/services/termsofuse.html This is an open-access article distributed under the terms described at http://journals.iucr.org/services/termsofuse.html.
spellingShingle Organic Papers
Peltier, Pauline
Daniellou, Richard
Roisnel, Thierry
Nugier-Chauvin, Caroline
Ferrières, Vincent
4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_full 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_fullStr 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_full_unstemmed 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_short 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_sort 4-nitro­phenyl α-l-rhamnopyran­oside hemihydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960228/
https://www.ncbi.nlm.nih.gov/pubmed/21201409
http://dx.doi.org/10.1107/S1600536807068195
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AT nugierchauvincaroline 4nitrophenylalrhamnopyranosidehemihydrate
AT ferrieresvincent 4nitrophenylalrhamnopyranosidehemihydrate

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