131245-85-7

Basic information

• Product Name: (1S,3R,5S)-5-Benzyloxy-cyclohexane-1,3-diol
• Synonyms: (1S,3R,5S)-5-Benzyloxy-cyclohexane-1,3-diol
• CAS NO: 131245-85-7
• Molecular Weight: 222.284
• Mol File: 131245-85-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1S,3R,5S)-5-Benzyloxy-cyclohexane-1,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3R,5S)-5-Benzyloxy-cyclohexane-1,3-diol(131245-85-7)
• EPA Substance Registry System: (1S,3R,5S)-5-Benzyloxy-cyclohexane-1,3-diol(131245-85-7)

Safety Data

• Hazardous Substances Data: 131245-85-7(Hazardous Substances Data)

Upstream product

• 95205-55-3 (1S,5R,7R)-3-Benzyloxymethyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol 
• 130323-27-2 (1S,5R,7R)-3-Hydroxymethyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol 
• 50409-12-6 cis,cis-1,3,5-trihydroxycyclohexane 
• 50409-13-7 2,5,11-trioxatricyclo[4.3.1.14,8 ] undecan-3-one 
• 100-44-7 benzyl chloride 
• 130256-33-6 (1R,5S,7R)-7-Benzyloxy-3-benzyloxymethyl-2,4-dioxa-bicyclo[3.3.1]nonane 
• 130256-34-7 meso-1,3-cis,3,5-cis-1,3-diacetoxy-5-benzyloxycyclohexane 

Downstream Products

• 130256-45-0 (R)-5-Benzyloxy-cyclohex-2-enone 
• 130256-46-1 cis-5-(benzyloxy)-3-cyclohexen-1-ol 
• 130256-34-7 (1R,3R,5R)-1,3-diacetoxy-5-benzyloxycyclohexane 
• 130256-36-9 (1S,3S,5R)-1-acetoxy-5-benzyloxy-3-cyclohexanol 
• 137767-18-1 (3R,5S)-5-benzyloxy-1-cyclohexen-3-ol 
• 131245-96-0 (2S,4R)-dimethyl 2-acetoxy-4-benzyloxyhexanedioate 
• 131245-97-1 (2S,4R)-dimethyl 4-benzyloxy-2-hydroxyhexanedioate 
• 131245-92-6 (4S,6R)-6-Benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-oxepan-2-one 
• 131245-93-7 (4R,6S)-4-Benzyloxy-6-(tert-butyl-dimethyl-silanyloxy)-oxepan-2-one 
• 131245-89-1 (3S,5R)-5-acetoxy-3-benzoyloxy-1-cyclohexene 
• 131245-98-2 (4R,6S)-4-benzyloxy-6-methoxycarbonyltetrahydro-2-pyranone 
• 131245-91-5 (3R,5S)-3-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-cyclohexanone 
• 131245-90-4 (1R,3S,5R)-3-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-cyclohexanol 
• 131245-99-3 (S,S)-1,3-dibenzyloxycyclohexane 

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.