5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one

In the title compound, C(6)H(10)N(2)O, the 2,3-dihydro-1H-pyrazole ring is approximately planar, with a maximum deviation of 0.013 (1) Å. Pairs of inter­molecular N—H⋯O hydrogen bonds link neighboring mol­ecules into dimers, generating R (2) (2)(8) ring motifs. These dimers are further linked into t...

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Autores principales: Shahani, Tara, Fun, Hoong-Kun, Ragavan, R. Venkat, Vijayakumar, V., Sarveswari, S.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979558/
https://www.ncbi.nlm.nih.gov/pubmed/21579442
http://dx.doi.org/10.1107/S160053681001696X
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author Shahani, Tara
Fun, Hoong-Kun
Ragavan, R. Venkat
Vijayakumar, V.
Sarveswari, S.
author_facet Shahani, Tara
Fun, Hoong-Kun
Ragavan, R. Venkat
Vijayakumar, V.
Sarveswari, S.
author_sort Shahani, Tara
collection PubMed
description In the title compound, C(6)H(10)N(2)O, the 2,3-dihydro-1H-pyrazole ring is approximately planar, with a maximum deviation of 0.013 (1) Å. Pairs of inter­molecular N—H⋯O hydrogen bonds link neighboring mol­ecules into dimers, generating R (2) (2)(8) ring motifs. These dimers are further linked into two-dimensional arrays parallel to the bc plane by inter­molecular N—H⋯O hydrogen bonds. The crystal structure is further stabilized by C—H⋯π inter­actions.
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spelling pubmed-29795582010-12-30 5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one Shahani, Tara Fun, Hoong-Kun Ragavan, R. Venkat Vijayakumar, V. Sarveswari, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(6)H(10)N(2)O, the 2,3-dihydro-1H-pyrazole ring is approximately planar, with a maximum deviation of 0.013 (1) Å. Pairs of inter­molecular N—H⋯O hydrogen bonds link neighboring mol­ecules into dimers, generating R (2) (2)(8) ring motifs. These dimers are further linked into two-dimensional arrays parallel to the bc plane by inter­molecular N—H⋯O hydrogen bonds. The crystal structure is further stabilized by C—H⋯π inter­actions. International Union of Crystallography 2010-05-15 /pmc/articles/PMC2979558/ /pubmed/21579442 http://dx.doi.org/10.1107/S160053681001696X Text en © Shahani et al. 2010 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
Shahani, Tara
Fun, Hoong-Kun
Ragavan, R. Venkat
Vijayakumar, V.
Sarveswari, S.
5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one
title 5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one
title_full 5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one
title_fullStr 5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one
title_full_unstemmed 5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one
title_short 5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one
title_sort 5-ethyl-4-methyl-1h-pyrazol-3(2h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979558/
https://www.ncbi.nlm.nih.gov/pubmed/21579442
http://dx.doi.org/10.1107/S160053681001696X
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AT ragavanrvenkat 5ethyl4methyl1hpyrazol32hone
AT vijayakumarv 5ethyl4methyl1hpyrazol32hone
AT sarveswaris 5ethyl4methyl1hpyrazol32hone

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