7115-22-2

Basic information

• Product Name: 1-O-benzoyl-2,3:5,6-di-O-isopropylidene-D-mannitol
• Synonyms: 1-O-benzoyl-2,3:5,6-di-O-isopropylidene-D-mannitol
• CAS NO: 7115-22-2
• Molecular Weight: 366.411
• Mol File: 7115-22-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-O-benzoyl-2,3:5,6-di-O-isopropylidene-D-mannitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-benzoyl-2,3:5,6-di-O-isopropylidene-D-mannitol(7115-22-2)
• EPA Substance Registry System: 1-O-benzoyl-2,3:5,6-di-O-isopropylidene-D-mannitol(7115-22-2)

Safety Data

• Hazardous Substances Data: 7115-22-2(Hazardous Substances Data)

Upstream product

• 3969-61-7 2,3,5,6-di-isopropyIidene-1,4-dihydroxy-D-mannitol 
• 98-88-4 benzoyl chloride 

Downstream Products

• 102487-51-4 Benzoic acid (4R,5R)-5-[(tert-butyl-dimethyl-silanyloxy)-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester 
• 102487-51-4 Benzoic acid (4R,5R)-5-[(R)-(tert-butyl-dimethyl-silanyloxy)-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester 
• 28910-22-7 Benzoic acid (4R,5R)-5-((R)-2,2-dimethyl-[1,3]dioxolane-4-carbonyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester 
• 102487-65-0 (S)-3-{(2S,3R)-3-[(4R,5S)-5-(Benzyloxycarbonylamino-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-oxiranyl}-3-hydroxy-propionic acid tert-butyl ester 
• 102487-62-7 (R)-3-{(2S,3R)-3-[(4R,5S)-5-(Benzyloxycarbonylamino-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-oxiranyl}-3-hydroxy-propionic acid tert-butyl ester 
• 102487-62-7 3-{(2S,3R)-3-[(4R,5S)-5-(Benzyloxycarbonylamino-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-oxiranyl}-3-hydroxy-propionic acid tert-butyl ester 
• 102487-63-8 3-{(2R,3R)-3-[(4R,5S)-5-(Benzyloxycarbonylamino-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-oxiranyl}-3-(tert-butyl-dimethyl-silanyloxy)-propionic acid tert-butyl ester 
• 102487-56-9 {(4S,5R)-5-[(R)-(tert-Butyl-dimethyl-silanyloxy)-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl}-carbamic acid benzyl ester 
• 102487-59-2 Methanesulfonic acid (2R,3R)-3-[(4S,5S)-5-(benzyloxycarbonylamino-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2,3-dihydroxy-propyl ester 
• 102487-57-0 {(4S,5R)-5-[(1R,2R)-1-(tert-Butyl-dimethyl-silanyloxy)-2,3-dihydroxy-propyl]-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl}-carbamic acid benzyl ester 
• 102487-58-1 [(4S,5S)-2,2-Dimethyl-5-((1R,2R)-1,2,3-trihydroxy-propyl)-[1,3]dioxolan-4-ylmethyl]-carbamic acid benzyl ester 
• 102487-60-5 [(4S,5S)-5-((R)-Hydroxy-(R)-oxiranyl-methyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl]-carbamic acid benzyl ester 
• 102518-70-7 [(4S,5R)-5-((2R,3S)-3-Hydroxymethyl-oxiranyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl]-carbamic acid benzyl ester 
• 102487-61-6 [(4S,5R)-5-((2S,3R)-3-Formyl-oxiranyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl]-carbamic acid benzyl ester 

Relevant articles and documents

TOTAL SYNTHESIS OF (+)-CASTANOSPERMINE FROM D-MANNOSE

A total synthesis of (+)-castanospermine (2) has been achieved starting from D-mannose by a route adopting a double-cyclization process (5c-6) as the key step.

The Baylis-Hillman reaction: a strategic tool for the synthesis of higher-carbon sugars

The Baylis-Hillman reaction of acyclic sugar-derived aldehydes is invoked as an attractive synthetic strategy for ready access to higher-carbon sugars.