291541-68-9

Basic information

• Product Name: (1R,2R,1'R,5'R)-2-(2'-aza-bicyclo[3.3.0]oct-2'-yl)-cyclohexan-1-ol
• Synonyms: (1R,2R,1'R,5'R)-2-(2'-aza-bicyclo[3.3.0]oct-2'-yl)-cyclohexan-1-ol
• CAS NO: 291541-68-9
• Molecular Weight: 209.332
• Mol File: 291541-68-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,2R,1'R,5'R)-2-(2'-aza-bicyclo[3.3.0]oct-2'-yl)-cyclohexan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,1'R,5'R)-2-(2'-aza-bicyclo[3.3.0]oct-2'-yl)-cyclohexan-1-ol(291541-68-9)
• EPA Substance Registry System: (1R,2R,1'R,5'R)-2-(2'-aza-bicyclo[3.3.0]oct-2'-yl)-cyclohexan-1-ol(291541-68-9)

Safety Data

• Hazardous Substances Data: 291541-68-9(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 156473-27-7 (3aR,6aR)-octahydrocyclopentapyrrole 
• 133696-29-4 (1R,5R)-2-(1-Cyclohexen-1-yl)-2-azabicyclo<3.3.0>octan 

Relevant articles and documents

Diastereoselective hydroboration of chiral enamines using an enantiomerically pure amine from an industrial waste material as the source of chirality

By a hydroboration/oxidation procedure trans-aminoalcohols with dr values from 74:26 to ≥95:5 were obtained. A bicyclic amine derived from the unnatural amino acid 2-azabicyclic[3.3.0]octane-3-carboxylic acid was used as the chiral precursor. The absolute