(Acetoxy)(2-methylphenyl)methyl acetate

In the title compound, C(12)H(14)O(4), the two acet­oxy groups are inclined by 57.92 (5)° and 62.71 (6)° to the benzene ring. An inter­molecular C—H⋯O inter­action involving the two acet­oxy groups generates a centrosymmetric dimer via an R (2) (2)(16) ring motif.

Detalles Bibliográficos
Autores principales: Kanchanadevi, J., Anbalagan, G., Saravanan, V., Mohanakrishnan, A. K., Manivannan, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213553/
https://www.ncbi.nlm.nih.gov/pubmed/22091130
http://dx.doi.org/10.1107/S1600536811028625
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author Kanchanadevi, J.
Anbalagan, G.
Saravanan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_facet Kanchanadevi, J.
Anbalagan, G.
Saravanan, V.
Mohanakrishnan, A. K.
Manivannan, V.
author_sort Kanchanadevi, J.
collection PubMed
description In the title compound, C(12)H(14)O(4), the two acet­oxy groups are inclined by 57.92 (5)° and 62.71 (6)° to the benzene ring. An inter­molecular C—H⋯O inter­action involving the two acet­oxy groups generates a centrosymmetric dimer via an R (2) (2)(16) ring motif.
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spelling pubmed-32135532011-11-16 (Acetoxy)(2-methylphenyl)methyl acetate Kanchanadevi, J. Anbalagan, G. Saravanan, V. Mohanakrishnan, A. K. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(14)O(4), the two acet­oxy groups are inclined by 57.92 (5)° and 62.71 (6)° to the benzene ring. An inter­molecular C—H⋯O inter­action involving the two acet­oxy groups generates a centrosymmetric dimer via an R (2) (2)(16) ring motif. International Union of Crystallography 2011-07-23 /pmc/articles/PMC3213553/ /pubmed/22091130 http://dx.doi.org/10.1107/S1600536811028625 Text en © Kanchanadevi et al. 2011 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
Kanchanadevi, J.
Anbalagan, G.
Saravanan, V.
Mohanakrishnan, A. K.
Manivannan, V.
(Acetoxy)(2-methylphenyl)methyl acetate
title (Acetoxy)(2-methylphenyl)methyl acetate
title_full (Acetoxy)(2-methylphenyl)methyl acetate
title_fullStr (Acetoxy)(2-methylphenyl)methyl acetate
title_full_unstemmed (Acetoxy)(2-methylphenyl)methyl acetate
title_short (Acetoxy)(2-methylphenyl)methyl acetate
title_sort (acetoxy)(2-methylphenyl)methyl acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213553/
https://www.ncbi.nlm.nih.gov/pubmed/22091130
http://dx.doi.org/10.1107/S1600536811028625
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AT anbalagang acetoxy2methylphenylmethylacetate
AT saravananv acetoxy2methylphenylmethylacetate
AT mohanakrishnanak acetoxy2methylphenylmethylacetate
AT manivannanv acetoxy2methylphenylmethylacetate

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