Acet­oxy-γ-valerolactone

Levulinyl cellulose esters have been produced as an effective renewable binder for architectural coatings. The title compound, C(7)H(10)O(4) (systematic name: 2-methyl-5-oxo­tetra­hydro­furan-2-yl acetate), assigned as the esterifying species, was isolated and crystallized to confirm the structure....

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Detalles Bibliográficos
Autores principales: Tristram, Cameron, Gainsford, Graeme J., Hinkley, Simon
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/PMC3685093/
https://www.ncbi.nlm.nih.gov/pubmed/23795112
http://dx.doi.org/10.1107/S1600536813013561
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author Tristram, Cameron
Gainsford, Graeme J.
Hinkley, Simon
author_facet Tristram, Cameron
Gainsford, Graeme J.
Hinkley, Simon
author_sort Tristram, Cameron
collection PubMed
description Levulinyl cellulose esters have been produced as an effective renewable binder for architectural coatings. The title compound, C(7)H(10)O(4) (systematic name: 2-methyl-5-oxo­tetra­hydro­furan-2-yl acetate), assigned as the esterifying species, was isolated and crystallized to confirm the structure. In the crystal, the mol­ecules pack in layers parallel to (102) utilizing weak C—H⋯O inter­actions.
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spelling pubmed-36850932013-06-21 Acet­oxy-γ-valerolactone Tristram, Cameron Gainsford, Graeme J. Hinkley, Simon Acta Crystallogr Sect E Struct Rep Online Organic Papers Levulinyl cellulose esters have been produced as an effective renewable binder for architectural coatings. The title compound, C(7)H(10)O(4) (systematic name: 2-methyl-5-oxo­tetra­hydro­furan-2-yl acetate), assigned as the esterifying species, was isolated and crystallized to confirm the structure. In the crystal, the mol­ecules pack in layers parallel to (102) utilizing weak C—H⋯O inter­actions. International Union of Crystallography 2013-05-25 /pmc/articles/PMC3685093/ /pubmed/23795112 http://dx.doi.org/10.1107/S1600536813013561 Text en © Tristram 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
Tristram, Cameron
Gainsford, Graeme J.
Hinkley, Simon
Acet­oxy-γ-valerolactone
title Acet­oxy-γ-valerolactone
title_full Acet­oxy-γ-valerolactone
title_fullStr Acet­oxy-γ-valerolactone
title_full_unstemmed Acet­oxy-γ-valerolactone
title_short Acet­oxy-γ-valerolactone
title_sort acet­oxy-γ-valerolactone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685093/
https://www.ncbi.nlm.nih.gov/pubmed/23795112
http://dx.doi.org/10.1107/S1600536813013561
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