N-Phenylpiperidine-1-carbothioamide
The title compound, C12H16N2S, was prepared by the reaction of with phenyl isothiocyanate and piperidine. In the crystal structure, the molecule exhibits intermolecular N—H...S hydrogen bonds and weak intramolecular C—H...S and C—H...N hydrogen-bonding interactions.
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
International Union of Crystallography
2008-09-01
|
Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536808025142 |
id |
doaj-f185bf2cb17e42bd9d41c18811a55d31 |
---|---|
record_format |
Article |
spelling |
doaj-f185bf2cb17e42bd9d41c18811a55d312020-11-24T21:55:29ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682008-09-01649o1743o174310.1107/S1600536808025142N-Phenylpiperidine-1-carbothioamideFang-Fang JianYu-Feng LiThe title compound, C12H16N2S, was prepared by the reaction of with phenyl isothiocyanate and piperidine. In the crystal structure, the molecule exhibits intermolecular N—H...S hydrogen bonds and weak intramolecular C—H...S and C—H...N hydrogen-bonding interactions.http://scripts.iucr.org/cgi-bin/paper?S1600536808025142 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fang-Fang Jian Yu-Feng Li |
spellingShingle |
Fang-Fang Jian Yu-Feng Li N-Phenylpiperidine-1-carbothioamide Acta Crystallographica Section E |
author_facet |
Fang-Fang Jian Yu-Feng Li |
author_sort |
Fang-Fang Jian |
title |
N-Phenylpiperidine-1-carbothioamide |
title_short |
N-Phenylpiperidine-1-carbothioamide |
title_full |
N-Phenylpiperidine-1-carbothioamide |
title_fullStr |
N-Phenylpiperidine-1-carbothioamide |
title_full_unstemmed |
N-Phenylpiperidine-1-carbothioamide |
title_sort |
n-phenylpiperidine-1-carbothioamide |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2008-09-01 |
description |
The title compound, C12H16N2S, was prepared by the reaction of with phenyl isothiocyanate and piperidine. In the crystal structure, the molecule exhibits intermolecular N—H...S hydrogen bonds and weak intramolecular C—H...S and C—H...N hydrogen-bonding interactions. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536808025142 |
work_keys_str_mv |
AT fangfangjian nphenylpiperidine1carbothioamide AT yufengli nphenylpiperidine1carbothioamide |
_version_ |
1725862342158188544 |