82769-20-8

Basic information

• Product Name: (+/-)-6-epimesembranol
• Synonyms: (+/-)-6-epimesembranol
• CAS NO: 82769-20-8
• Molecular Weight: 291.39
• Mol File: 82769-20-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (+/-)-6-epimesembranol(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-6-epimesembranol(82769-20-8)
• EPA Substance Registry System: (+/-)-6-epimesembranol(82769-20-8)

Safety Data

• Hazardous Substances Data: 82769-20-8(Hazardous Substances Data)

Upstream product

• 82769-19-5 (+/-)-mesembranol 
• 125032-05-5 (1R^*,2S^*,4R^*)-4-(benzyloxy)-2-bromo-1-(3,4-dimethoxyphenyl)cyclohexan-1-ol 
• 92829-83-9 1,4-dioxaspiro<4,5>decan-8-ol benzyl ether 
• 82732-16-9 4-(benzyloxy)-1-(3,4-dimethoxyphenyl)cyclohex-1-ene 
• 2987-06-6 4-(benzyloxy)cyclohexanone 
• 22428-87-1 4,4-ethylenedioxycyclohexan-1-ol 
• 50-00-0 formaldehyd 
• 82732-19-2 1-methyl-3a-(3,4-dimethoxyphenyl)-6-(benzyloxy)-cis-octahydroindole 
• 21104-32-5 (3aR,7aR)-3a-(3,4-Dimethoxy-phenyl)-6-hydroxy-1-methyl-octahydro-indol-2-one 
• 6023-73-0 mesembrine 
• 82732-24-9 (1S,6R)-4-Benzyloxy-8,8-dichloro-1-(3,4-dimethoxy-phenyl)-bicyclo[4.2.0]octan-7-one 
• 82732-18-1 1-methyl-3a-(3,4-dimethoxyphenyl)-6-(benzyloxy)-cis-octahydroindol-2-one 
• 82732-17-0 1-(3,4-dimethoxyphenyl)-4-(benzyloxy)-cis-bicyclo<4.2.0>octan-7-one 
• 125032-07-7 (1S^*,2R^*,5R^*)-N-<5-(benzyloxy)-2-hydroxy-2-(3,4-dimethoxyphenyl)cyclohex-1-yl>-α,α-dichloro-N-methylacetamide 

Downstream Products

• 6023-73-0 mesembrine 

Relevant articles and documents

A general efficient strategy for cis-3a-aryloctahydroindole alkaloids via stereocontrolled ZnBr2-catalyzed rearrangement of 2,3-aziridino alcohols

(Matrix presented) A short and general approach to the cis-3a-aryloctahydroindole alkaloids has been developed on the basis of a key stereocontrolled ZnBr2-catalyzed rearrangement of 2,3-aziridino alcohols. Two representative members, (±)-crina

Synthesis of (+/-)-Mesembranol by Radical Cyclisation of α,α-Dichloroacetamides

(+/-)-Mesembranol was synthesised in a highly stereoselective manner using Bu3SnH mediated radical cyclisation of α,α-dichloroacetamide as the key step.