Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate

In the title compound, C(16)H(20)N(2)O(2), the pyrazole ring is essentially planar [maximum deviation = 0.008 (2) Å] and is inclined at an angle of 82.82 (10)° with respect to the phenyl ring. The crystal packing is consolidated by pairs of inter­molecular C—H⋯O hydrogen bonds, which link the mol­ec...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Quah, Ching Kheng, Chandrakantha, B., Isloor, Arun M., Shetty, Prakash
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007952/
https://www.ncbi.nlm.nih.gov/pubmed/21588598
http://dx.doi.org/10.1107/S1600536810030643
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author Fun, Hoong-Kun
Quah, Ching Kheng
Chandrakantha, B.
Isloor, Arun M.
Shetty, Prakash
author_facet Fun, Hoong-Kun
Quah, Ching Kheng
Chandrakantha, B.
Isloor, Arun M.
Shetty, Prakash
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(16)H(20)N(2)O(2), the pyrazole ring is essentially planar [maximum deviation = 0.008 (2) Å] and is inclined at an angle of 82.82 (10)° with respect to the phenyl ring. The crystal packing is consolidated by pairs of inter­molecular C—H⋯O hydrogen bonds, which link the mol­ecules into centrosymmetric dimers stacked along the a axis.
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spelling pubmed-30079522010-12-30 Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate Fun, Hoong-Kun Quah, Ching Kheng Chandrakantha, B. Isloor, Arun M. Shetty, Prakash Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(20)N(2)O(2), the pyrazole ring is essentially planar [maximum deviation = 0.008 (2) Å] and is inclined at an angle of 82.82 (10)° with respect to the phenyl ring. The crystal packing is consolidated by pairs of inter­molecular C—H⋯O hydrogen bonds, which link the mol­ecules into centrosymmetric dimers stacked along the a axis. International Union of Crystallography 2010-08-11 /pmc/articles/PMC3007952/ /pubmed/21588598 http://dx.doi.org/10.1107/S1600536810030643 Text en © Fun 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
Fun, Hoong-Kun
Quah, Ching Kheng
Chandrakantha, B.
Isloor, Arun M.
Shetty, Prakash
Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate
title Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate
title_full Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate
title_fullStr Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate
title_full_unstemmed Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate
title_short Ethyl 1-tert-butyl-5-phenyl-1H-pyrazole-4-carboxyl­ate
title_sort ethyl 1-tert-butyl-5-phenyl-1h-pyrazole-4-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007952/
https://www.ncbi.nlm.nih.gov/pubmed/21588598
http://dx.doi.org/10.1107/S1600536810030643
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AT isloorarunm ethyl1tertbutyl5phenyl1hpyrazole4carboxylate
AT shettyprakash ethyl1tertbutyl5phenyl1hpyrazole4carboxylate

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