95205-55-3

Basic information

• Product Name: (1S,5R,7R)-3-Benzyloxymethyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol
• CAS NO: 95205-55-3
• Molecular Weight: 264.321
• Mol File: 95205-55-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,5R,7R)-3-Benzyloxymethyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,5R,7R)-3-Benzyloxymethyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol(95205-55-3)
• EPA Substance Registry System: (1S,5R,7R)-3-Benzyloxymethyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol(95205-55-3)

Safety Data

• Hazardous Substances Data: 95205-55-3(Hazardous Substances Data)

Upstream product

• 50409-12-6 cis,cis-1,3,5-trihydroxycyclohexane 
• 50409-13-7 2,5,11-trioxatricyclo[4.3.1.14,8 ] undecan-3-one 
• 100-39-0 benzyl bromide 
• 130323-27-2 (1S,5R,7R)-3-Hydroxymethyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol 

Downstream Products

• 130256-33-6 (1R,5S,7R)-7-Benzyloxy-3-benzyloxymethyl-2,4-dioxa-bicyclo[3.3.1]nonane 
• 130256-43-8 (S)-5-(benzyloxymethyl)-3-methylcyclohex-2-enone 
• 130256-49-4 (R)-5-(benzyloxymethyl)-3-methylcyclohex-2-enone 
• 130256-41-6 (R)-3-Benzyloxymethyl-cyclohexanone 
• 130256-47-2 (S)-3-Benzyloxymethyl-cyclohexanone 
• 130256-40-5 (R)-5-benzyloxymethyl-2-cyclohexenone 
• 130256-48-3 5(S)-benzyloxymethyl-2-cyclohexenone 
• 130256-35-8 Butyric acid (1R,3R,5S)-3-benzyloxy-5-butyryloxy-cyclohexyl ester 
• 130256-42-7 (3R,5R)-5-Benzyloxymethyl-3-methyl-2-phenylselanyl-cyclohexanone 
• 130256-38-1 cis-5-benzyloxymethyl-1,3-diacetoxycyclohexane 
• 130256-34-7 meso-1,3-cis,3,5-cis-1,3-diacetoxy-5-benzyloxycyclohexane 
• 130256-39-2 Acetic acid (1S,3S,5R)-3-benzyloxymethyl-5-hydroxy-cyclohexyl ester 
• 130256-37-0 (1S,5R)-3-Benzyloxymethyl-7-methylene-2,4-dioxa-bicyclo[3.3.1]nonane 
• 130256-36-9 Acetic acid (1R,3S,5R)-3-benzyloxy-5-hydroxy-cyclohexyl ester 

Relevant articles and documents

ENANTIOTOPOSELECTIVE PLE-CATALYZED HYDROLYSIS OF CIS-5-SUBSTITUTED-1,3-DIACYLOXYCYCLOHEXANES. PREPARATION OF SOME USEFUL CHIRAL BUILDING BLOCKS

PLE-catalyzed hydrolysis of prochiral cis-5-benzyloxymethyl-1,3-diacetoxycyclohexane and cis-5-benzyloxy-1,3-diacetoxycyclohexane proceeds with high enantiotoposelectivity.The preparation of some useful chiral building blocks is described.