126004-02-2

Basic information

• Product Name: (1R,2R,5R)-3-[(E)-(S)-2-(3-Methoxy-phenyl)-1-phenyl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol
• CAS NO: 126004-02-2
• Molecular Weight: 377.527
• Mol File: 126004-02-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,2R,5R)-3-[(E)-(S)-2-(3-Methoxy-phenyl)-1-phenyl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,5R)-3-[(E)-(S)-2-(3-Methoxy-phenyl)-1-phenyl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(126004-02-2)
• EPA Substance Registry System: (1R,2R,5R)-3-[(E)-(S)-2-(3-Methoxy-phenyl)-1-phenyl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(126004-02-2)

Safety Data

• Hazardous Substances Data: 126004-02-2(Hazardous Substances Data)

Upstream product

• 126003-96-1 C₁₇H₂₃NO 

Downstream Products

• 67553-41-7 pinanone oxime 
• 109430-87-7 (S)-(+)-2-(3-methoxyphenyl)-1-phenylethylamine 

Relevant articles and documents

ASYMMETRIC SYNTHESIS VIII: ENANTIONSELECTIVE SYNTHESIS OF (R) OR (S)-α-SUBSTITUTED BENZYLAMINES VIA CHIRAL PINANONE KETIMINE TEMPLATE

An excellent asymmetric synthesis of both (R) and (S)-α-substituted benzylamines in optical purity 90.4 - 99.9percent has been achieved by alkylation of a chiral ketimine, prepared from pinanone and benzylamine.Diastereoselectivity in the alkylation is not dependent on the alkyl halides.