1356856-79-5

Basic information

• Product Name: (5R,7R)-[3,3,0']-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-hydroxybicyclooctane
• Synonyms: (5R,7R)-[3,3,0']-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-hydroxybicyclooctane
• CAS NO: 1356856-79-5
• Molecular Weight: 407.553
• Mol File: 1356856-79-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (5R,7R)-[3,3,0']-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-hydroxybicyclooctane(CAS DataBase Reference)
• NIST Chemistry Reference: (5R,7R)-[3,3,0']-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-hydroxybicyclooctane(1356856-79-5)
• EPA Substance Registry System: (5R,7R)-[3,3,0']-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-hydroxybicyclooctane(1356856-79-5)

Safety Data

• Hazardous Substances Data: 1356856-79-5(Hazardous Substances Data)

Upstream product

• 923985-59-5 (2R,4R)-4-hydroxyproline-N-ethyl carbamate methyl ester 

Downstream Products

• 1379466-19-9 (5R,7R)-[3,3,0]-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-(ethylcarbamoyloxy)bicyclooctane 
• 1379466-21-3 (5R,7R)-[3,3,0]-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-(octylcarbamoyloxy)bicyclooctane 
• 1379466-22-4 (2R,4R)-2-(bis-(4'-t-butylphenyl)methyl)-4-(octylcarbamoyloxy)pyrrolidine 
• 1379466-23-5 (5R,7R)-[3,3,0]-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-(diphenylcarbamoyloxy)bicyclooctane 
• 1379466-24-6 (2R,4R)-2-(bis-(4'-t-butylphenyl)methyl)-4-(diphenylcarbamoyloxy)pyrrolidine 
• 1379466-20-2 (2R,4R)-2-(bis-(4'-t-butylphenyl)methyl)-4-(ethylcarbamoyloxy)pyrrolidine 
• 1379466-15-5 (5R,7R)-[3,3,0]-1-aza-2-oxo-3-oxa-4,4-bis-(4'-t-butylphenyl)-7-(butylcarbamoyloxy)bicyclooctane 

Relevant articles and documents

METHOD FOR MANUFACTURING OPTICALLY ACTIVE MENTHOL

An object of the present invention is to provide a method for manufacturing an optically active menthol having fewer steps, which generates less environmentally polluting waste because a catalytic reaction is involved in all of the steps, and is capable of saving a production cost. The present invention relates to a method for manufacturing an optically active menthol, including the following steps: A-1) asymmetrically hydrogenating at least one of geranial and neral to thereby obtain an optically active citronellal, B-1) conducting a ring-closure reaction of the optically active citronellal in the presence of an acid catalyst to thereby obtain an optically active isopulegol, and C-1) hydrogenating the optically active isopulegol to thereby obtain an optically active menthol.