Synthesis and Conformational Study of Stereoisomeric 2-Phenyl-4a,5,6,7,8,8a-hexahydro-4H-1,3,4-benzoxadiazines was written by Rosling, Ari;Fulop, Ferenc;Askolin, Curt-Peter;Mattinen, Jorma. And the article was included in Journal of Chemical Research, Synopses in 1998.SDS of cas: 40571-86-6 This article mentions the following:
New stereoisomeric hexahydro-4H-1,3,4-benzoxadiazines were synthesized and their conformational behavior, ring and nitrogen inversion, was investigated by means of NMR spectroscopy and 1H NMR simulation. In the experiment, the researchers used many compounds, for example, Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6SDS of cas: 40571-86-6).
Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 40571-86-6
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts