160694-00-8

Basic information

• Product Name: (9S,13S)-5,6,8,14-Tetrahydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-8-hydroxy-3-methoxymorphinan-7-one
• Synonyms: (9S,13S)-5,6,8,14-Tetrahydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-8-hydroxy-3-methoxymorphinan-7-one
• CAS NO: 160694-00-8
• Molecular Weight: 523.585
• Mol File: 160694-00-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (9S,13S)-5,6,8,14-Tetrahydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-8-hydroxy-3-methoxymorphinan-7-one(CAS DataBase Reference)
• NIST Chemistry Reference: (9S,13S)-5,6,8,14-Tetrahydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-8-hydroxy-3-methoxymorphinan-7-one(160694-00-8)
• EPA Substance Registry System: (9S,13S)-5,6,8,14-Tetrahydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-8-hydroxy-3-methoxymorphinan-7-one(160694-00-8)

Safety Data

• Hazardous Substances Data: 160694-00-8(Hazardous Substances Data)

Upstream product

• 115-53-7 sinomenine 
• 100-51-6 benzyl alcohol 
• 164738-86-7 (6R,9S,13R,14S)-7,8-Didehydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-3,7-dimethoxymorphinan-6-ol 
• 160693-97-0 (6S,9S,13R,14S)-7,8-Didehydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-3,7-dimethoxymorphinan-6-ol 
• 160693-98-1 (6R,9S,13R,14S)-7,8-Didehydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-3,7-dimethoxy-6-<(2-nitrophenyl)seleno>morphinane 
• 164738-89-0 (6S,9S,13R,14S)-7,8-Didehydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-3,7-dimethoxy-6-<(2-nitrophenyl)seleno>morphinane 
• 160693-96-9 (9S,13R,14S)-7,8-Dehydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-3,7-dimethoxymorphinan-6-one 
• 160693-95-8 O-Benzylsinomenine 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 160693-99-2 (8S,9S,13R,14S)-5,6-Didehydro-4-(benzyloxy)-17-<(benzyloxy)carbonyl>-8-hydroxy-3-methoxymorphinan-7-one 

Relevant articles and documents

Syntheses of Antitumor Morphinane Alkaloids, Sinococuline and 6-epi-, 7-epi-, and 6-epi-7-epi-Sinococuline, from Sinomenine

An antitumor alkaloid, sinococuline 81), and its C-6 and/or C-7 epimeric analogs 3-5 have been synthesized from sinomenine (2).The carbonyl transposition from 9 to 8 using selenoxide chemistry proceeded in an efficient manner.Successive C-6 hydroxylation