<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>43</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>64(Pt 7)</volume><submitter>Zia-Ur-Rehman M</submitter><pubmed_abstract>In the mol-ecule of the title compound, C(10)H(9)N(3)O(2), the pyrazole ring is approximately coplanar with the amino and carboxyl groups. The phenyl group is twisted by 48.13 (3)° relative to this plane. An intra-molecular N-H⋯O hydrogen bond stabilizes the planar conformation of the mol-ecule. The mol-ecules are linked into two-dimensional sheets by two strong inter-molecular N-H⋯N and O-H⋯O hydrogen bonds. The latter forms the classic carboxylic acid dimer motif.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o1312-3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2961688</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>5-Amino-1-phenyl-1H-pyrazole-4-carboxylic acid.</pubmed_title><pmcid>PMC2961688</pmcid><pubmed_authors>Elsegood MR</pubmed_authors><pubmed_authors>Zia-Ur-Rehman M</pubmed_authors><pubmed_authors>Akbar N</pubmed_authors><pubmed_authors>Shah Zaib Saleem R</pubmed_authors><view_count>43</view_count></additional><is_claimable>false</is_claimable><name>5-Amino-1-phenyl-1H-pyrazole-4-carboxylic acid.</name><description>In the mol-ecule of the title compound, C(10)H(9)N(3)O(2), the pyrazole ring is approximately coplanar with the amino and carboxyl groups. The phenyl group is twisted by 48.13 (3)° relative to this plane. An intra-molecular N-H⋯O hydrogen bond stabilizes the planar conformation of the mol-ecule. The mol-ecules are linked into two-dimensional sheets by two strong inter-molecular N-H⋯N and O-H⋯O hydrogen bonds. The latter forms the classic carboxylic acid dimer motif.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Jun</publication><modification>2024-12-04T10:41:52.196Z</modification><creation>2019-03-27T00:00:01Z</creation></dates><accession>S-EPMC2961688</accession><cross_references><pubmed>21202940</pubmed><doi>10.1107/S1600536808018394</doi></cross_references></HashMap>