288622-62-8

Basic information

• Product Name: 3(2H)-Indolizinone, hexahydro-6,7,8-trihydroxy-8a-methoxy-, (6S,7S,8S,8aS)- (9CI)
• Synonyms: 3(2H)-Indolizinone, hexahydro-6,7,8-trihydroxy-8a-methoxy-, (6S,7S,8S,8aS)- (9CI)
• CAS NO: 288622-62-8
• Molecular Formula: C9H15NO5
• Molecular Weight: 217.2191
• Product Categories: ALCOHOL
• Mol File: 288622-62-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3(2H)-Indolizinone, hexahydro-6,7,8-trihydroxy-8a-methoxy-, (6S,7S,8S,8aS)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3(2H)-Indolizinone, hexahydro-6,7,8-trihydroxy-8a-methoxy-, (6S,7S,8S,8aS)- (9CI)(288622-62-8)
• EPA Substance Registry System: 3(2H)-Indolizinone, hexahydro-6,7,8-trihydroxy-8a-methoxy-, (6S,7S,8S,8aS)- (9CI)(288622-62-8)

Safety Data

• Hazardous Substances Data: 288622-62-8(Hazardous Substances Data)

Upstream product

• 288622-59-3 8-azido-2,3,8-trideoxy-4,5-O-isopropylidene-α-L-erythro-oct-4,6-diulofuranosononitrile 
• 288622-60-6 8-azido-2,3,8-trideoxy-4,5-O-isopropylidene-α-L-ribo-oct-4-ulofuranosononitrile 
• 242129-66-4 8-azido-2,3,8-trideoxy-4,5-O-isopropylidene-α-L-xylo-oct-4-ulo-4,7-furanosononitrile 
• 67-56-1 methanol 
• 288622-61-7 8-azido-2,3,8-trideoxy-L-ribo-oct-4-ulosononitrile 

Relevant articles and documents

Synthesis of 4-octuloses, VI([≠]) - 4-Octulose derivatives, prepared from 1-sorbose, as key intermediates in the stereoselective synthesis of C- glycoside and polyhydroxyindolizidine analogues

Reactions of 1 and 12 with p-toluenesulfonyl chloride in pyridine gave the corresponding 1-O-p-toluenesulfonyl derivatives 2 and 13 in yields of 91% and 60%, respectively. Compound 12 was also transformed into 14 by treatment with I2/Ph3/