<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>75(Pt 10)</volume><submitter>Asgarova AR</submitter><pubmed_abstract>In the title compound, C24H31N3O2, the mean plane of the central pyrazole ring [r.m.s. deviation = 0.095?Å] makes dihedral angles of 11.93?(9) and 84.53?(8)°, respectively, with the phenyl and benzene rings. There is a short intra-molecular N-H?N contact, which generates an S(5) ring motif. In the crystal, pairs of N-H?O hydrogen bonds link inversion-related mol-ecules into dimers, generating an R 2 2(8) ring motif. The Hirshfeld surface analysis indicates that the most significant contribution involves H?H contacts of 68.6.</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>1467-1471</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6775746</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Crystal structure and Hirshfeld surface analysis of 5-(3,5-di-tert-butyl-4-hy-droxy-phen-yl)-3-phenyl-4,5-di-hydro-1H-pyrazole-1-carboxamide.</pubmed_title><pmcid>PMC6775746</pmcid><pubmed_authors>Asgarova AR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystal structure and Hirshfeld surface analysis of 5-(3,5-di-tert-butyl-4-hy-droxy-phen-yl)-3-phenyl-4,5-di-hydro-1H-pyrazole-1-carboxamide.</name><description>In the title compound, C24H31N3O2, the mean plane of the central pyrazole ring [r.m.s. deviation = 0.095?Å] makes dihedral angles of 11.93?(9) and 84.53?(8)°, respectively, with the phenyl and benzene rings. There is a short intra-molecular N-H?N contact, which generates an S(5) ring motif. In the crystal, pairs of N-H?O hydrogen bonds link inversion-related mol-ecules into dimers, generating an R 2 2(8) ring motif. The Hirshfeld surface analysis indicates that the most significant contribution involves H?H contacts of 68.6.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2021-03-13T08:08:38Z</modification><creation>2019-11-05T08:05:08Z</creation></dates><accession>S-EPMC6775746</accession><cross_references><pubmed>31636977</pubmed><doi>10.1107/S205698901901243X</doi></cross_references></HashMap>