(E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate

The configuration of the thione–aryl C—N single bond in the title mol­ecule, C(10)H(12)N(2)O(3)S, is E. Centrosymmetrically related mol­ecules are connected into a dimer via an eight-membered thio­amide {⋯H—N—C=S}(2) synthon and mol­ecules are consolidated into the crystal structure via C—H⋯O inter­...

Descripción completa

Detalles Bibliográficos
Autores principales: Ellis, Carol A., Tiekink, Edward R. T., Zukerman-Schpector, Julio
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2007
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915386/
https://www.ncbi.nlm.nih.gov/pubmed/21200907
http://dx.doi.org/10.1107/S1600536807067360
_version_ 1782184928617693184
author Ellis, Carol A.
Tiekink, Edward R. T.
Zukerman-Schpector, Julio
author_facet Ellis, Carol A.
Tiekink, Edward R. T.
Zukerman-Schpector, Julio
author_sort Ellis, Carol A.
collection PubMed
description The configuration of the thione–aryl C—N single bond in the title mol­ecule, C(10)H(12)N(2)O(3)S, is E. Centrosymmetrically related mol­ecules are connected into a dimer via an eight-membered thio­amide {⋯H—N—C=S}(2) synthon and mol­ecules are consolidated into the crystal structure via C—H⋯O inter­actions.
format Text
id pubmed-2915386
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29153862010-12-30 (E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate Ellis, Carol A. Tiekink, Edward R. T. Zukerman-Schpector, Julio Acta Crystallogr Sect E Struct Rep Online Organic Papers The configuration of the thione–aryl C—N single bond in the title mol­ecule, C(10)H(12)N(2)O(3)S, is E. Centrosymmetrically related mol­ecules are connected into a dimer via an eight-membered thio­amide {⋯H—N—C=S}(2) synthon and mol­ecules are consolidated into the crystal structure via C—H⋯O inter­actions. International Union of Crystallography 2007-12-21 /pmc/articles/PMC2915386/ /pubmed/21200907 http://dx.doi.org/10.1107/S1600536807067360 Text en © Ellis et al. 2008 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
Ellis, Carol A.
Tiekink, Edward R. T.
Zukerman-Schpector, Julio
(E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate
title (E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate
title_full (E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate
title_fullStr (E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate
title_full_unstemmed (E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate
title_short (E)-O-Isopropyl N-(4-nitro­phen­yl)thio­carbamate
title_sort (e)-o-isopropyl n-(4-nitro­phen­yl)thio­carbamate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915386/
https://www.ncbi.nlm.nih.gov/pubmed/21200907
http://dx.doi.org/10.1107/S1600536807067360
work_keys_str_mv AT elliscarola eoisopropyln4nitrophenylthiocarbamate
AT tiekinkedwardrt eoisopropyln4nitrophenylthiocarbamate
AT zukermanschpectorjulio eoisopropyln4nitrophenylthiocarbamate

Ejemplares similares