<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>45</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>65(Pt 10)</volume><submitter>Cibian M</submitter><pubmed_abstract>The title compound, 2C(17)H(20)N(2)O·CH(2)Cl(2), was obtained by N-oxidation of the parent formamidine with m-chloro-peroxy-benzoic acid (m-CPBA). This is the first use of the above-mentioned synthetic route for the preparation of hydroxy-amidines. The title compound crystallizes as a cyclic dimer resulting from the presence of O-H?O and N-H?N hydrogen bonds.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o2485</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2970452</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>N,N-Bis-(2,6-di-methyl-phen-yl)-N-hydroxyformamidine N,N'-bis-(2,6-dimethyl-phen-yl)-N-oxidoformamidinium dichloro-methane solvate.</pubmed_title><pmcid>PMC2970452</pmcid><pubmed_authors>Derossi S</pubmed_authors><pubmed_authors>Hanan GS</pubmed_authors><pubmed_authors>Cibian M</pubmed_authors><view_count>45</view_count></additional><is_claimable>false</is_claimable><name>N,N-Bis-(2,6-di-methyl-phen-yl)-N-hydroxyformamidine N,N'-bis-(2,6-dimethyl-phen-yl)-N-oxidoformamidinium dichloro-methane solvate.</name><description>The title compound, 2C(17)H(20)N(2)O·CH(2)Cl(2), was obtained by N-oxidation of the parent formamidine with m-chloro-peroxy-benzoic acid (m-CPBA). This is the first use of the above-mentioned synthetic route for the preparation of hydroxy-amidines. The title compound crystallizes as a cyclic dimer resulting from the presence of O-H?O and N-H?N hydrogen bonds.</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Sep</publication><modification>2021-02-21T07:32:34Z</modification><creation>2019-03-27T00:00:15Z</creation></dates><accession>S-EPMC2970452</accession><cross_references><pubmed>21577936</pubmed><doi>10.1107/S1600536809036708</doi></cross_references></HashMap>