117514-02-0

Basic information

• Product Name: methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-vinyl-α-D-erythro-hex-2-enopyranoside
• Synonyms: methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-vinyl-α-D-erythro-hex-2-enopyranoside
• CAS NO: 117514-02-0
• Molecular Weight: 274.317
• Mol File: 117514-02-0.mol

Chemical Properties

• CAS DataBase Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-vinyl-α-D-erythro-hex-2-enopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-vinyl-α-D-erythro-hex-2-enopyranoside(117514-02-0)
• EPA Substance Registry System: methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-vinyl-α-D-erythro-hex-2-enopyranoside(117514-02-0)

Safety Data

• Hazardous Substances Data: 117514-02-0(Hazardous Substances Data)

Upstream product

• 3150-15-0 methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside 
• 27200-84-6 methyl triphenylphosphonium bromide 
• 117513-99-2 methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-formyl-α-D-erythro-hex-2-enopyranoside 

Downstream Products

• 130222-79-6 (2aR,6S,8R,8aS,8bS)-8-Benzyloxymethyl-6-methoxy-2a,4,6,8,8a,8b-hexahydro-2H,3H-furo[2,3,4-de]isochromene 
• 130222-79-6 (2aS,6S,8R,8aS,8bS)-8-Benzyloxymethyl-6-methoxy-2a,4,6,8,8a,8b-hexahydro-2H,3H-furo[2,3,4-de]isochromene 
• 130222-81-0 (2R,3S,6S)-3-Allyloxy-2-benzyloxymethyl-6-methoxy-5-vinyl-3,6-dihydro-2H-pyran 
• 130222-80-9 (2R,3S,6S)-2-Benzyloxymethyl-6-methoxy-5-vinyl-3,6-dihydro-2H-pyran-3-ol 

Relevant articles and documents

Efficient routes to pyranosidic homologated conjugated enals and dienes from monosaccharides

Three new processes for the obtention of pyranosidic dienes type B, and D and homologated conjugated enals A, have been designed in the context of the preparation of useful chiral building blocks from monosaccharides. Addition of vinylmagnesium bromide on

Straightforward Route to 2- and 3-Formyl Hex-1- and -2-enopyranosides and Their highly Stereoselective Hetero Diels-Alder Reaction with Ethyl Vinyl Ether

A straightforward route from D-glucose to conjugated enal and diene pyranoses through a dithiane-based methodology is disclosed; hetero Diels-Alder reaction of the enals with ethyl vinyl ether occurs with high stereoselectivity.