5-Iodo-3-phenyl-2,1-benzoxazole

The title compound, C(13)H(8)INO, was prepared by a condensation reaction of 4-nitro­benzene with phenyl­acetonitrile in NaOH–ethanol solution. There are two independent mol­ecules in the asymmetric unit, in which the dihedral angles between the benzene ring and the benzoisoxazole unit are 4.2 (3) a...

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Autores principales: Teslenko, Yuriy, Matiychuk, Vasyl S., Kinzhybalo, Vasyl, Lis, Tadeusz, Obushak, Mykola D.
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/PMC3629537/
https://www.ncbi.nlm.nih.gov/pubmed/23634055
http://dx.doi.org/10.1107/S1600536813005862
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author Teslenko, Yuriy
Matiychuk, Vasyl S.
Kinzhybalo, Vasyl
Lis, Tadeusz
Obushak, Mykola D.
author_facet Teslenko, Yuriy
Matiychuk, Vasyl S.
Kinzhybalo, Vasyl
Lis, Tadeusz
Obushak, Mykola D.
author_sort Teslenko, Yuriy
collection PubMed
description The title compound, C(13)H(8)INO, was prepared by a condensation reaction of 4-nitro­benzene with phenyl­acetonitrile in NaOH–ethanol solution. There are two independent mol­ecules in the asymmetric unit, in which the dihedral angles between the benzene ring and the benzoisoxazole unit are 4.2 (3) and 4.1 (3)°. The crystal packing is governed by C—H⋯N, C—I⋯π and C—I⋯O inter­actions.
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spelling pubmed-36295372013-04-30 5-Iodo-3-phenyl-2,1-benzoxazole Teslenko, Yuriy Matiychuk, Vasyl S. Kinzhybalo, Vasyl Lis, Tadeusz Obushak, Mykola D. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(8)INO, was prepared by a condensation reaction of 4-nitro­benzene with phenyl­acetonitrile in NaOH–ethanol solution. There are two independent mol­ecules in the asymmetric unit, in which the dihedral angles between the benzene ring and the benzoisoxazole unit are 4.2 (3) and 4.1 (3)°. The crystal packing is governed by C—H⋯N, C—I⋯π and C—I⋯O inter­actions. International Union of Crystallography 2013-03-09 /pmc/articles/PMC3629537/ /pubmed/23634055 http://dx.doi.org/10.1107/S1600536813005862 Text en © Teslenko 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
Teslenko, Yuriy
Matiychuk, Vasyl S.
Kinzhybalo, Vasyl
Lis, Tadeusz
Obushak, Mykola D.
5-Iodo-3-phenyl-2,1-benzoxazole
title 5-Iodo-3-phenyl-2,1-benzoxazole
title_full 5-Iodo-3-phenyl-2,1-benzoxazole
title_fullStr 5-Iodo-3-phenyl-2,1-benzoxazole
title_full_unstemmed 5-Iodo-3-phenyl-2,1-benzoxazole
title_short 5-Iodo-3-phenyl-2,1-benzoxazole
title_sort 5-iodo-3-phenyl-2,1-benzoxazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629537/
https://www.ncbi.nlm.nih.gov/pubmed/23634055
http://dx.doi.org/10.1107/S1600536813005862
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AT kinzhybalovasyl 5iodo3phenyl21benzoxazole
AT listadeusz 5iodo3phenyl21benzoxazole
AT obushakmykolad 5iodo3phenyl21benzoxazole

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