303752-88-7

Basic information

• Product Name: Allyl 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranoside
• Synonyms: Allyl 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranoside
• CAS NO: 303752-88-7
• Molecular Weight: 488.58
• Mol File: 303752-88-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Allyl 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranoside(303752-88-7)
• EPA Substance Registry System: Allyl 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranoside(303752-88-7)

Safety Data

• Hazardous Substances Data: 303752-88-7(Hazardous Substances Data)

Upstream product

• 10343-15-4 allyl 2,3,4,6-tetra-O-acetyl-D-galactopyranoside 
• 2595-07-5 allyl D-galactopyranoside 
• 100-52-7 benzaldehyde 
• 25878-60-8 D-galactose pentaacetate 
• 3006-41-5 4,6-O-benzylidene-α,β-D-galactopyranose 
• 100-39-0 benzyl bromide 
• 20746-64-9 (2S,4aR,7R,8R,8aR)-6-Allyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 

Downstream Products

• 119237-99-9 <2S-(2α,4aβ,5α,6β,7α,7aβ)>-Hexahydro-5-methyl-2-phenyl-6,7-bis(phenylmethoxy)cyclopenta-1,3-dioxin 
• 119111-07-8 (S)-1,2-Dideoxy-3,4-bis-O-(phenylmethyl)-5,7-O-(phenylmethylene)-D-galacto-hept-1-enitol 
• 119111-36-3 Imidazole-1-carbothioic acid O-[(2S,4S,5R)-4-((1R,2S)-1,2-bis-benzyloxy-but-3-enyl)-2-phenyl-[1,3]dioxan-5-yl] ester 
• 303752-91-2 1-O-(2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-2-O-methanesulfonyl-D-arabino-1,2,3,4-octadecantetrol 
• 303752-86-5 (2S,3S,4R)-2-azido-1-(((2S,4aS,6S,7R,8S,8aR)-7,8-bis(benzyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-6-yl)oxy)octadecane-3,4-diol 
• 303752-87-6 O-(2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl) trichloroacetimidate 
• 168037-64-7 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranose 

Relevant articles and documents

Total synthesis of α-galactosyl cerebroside

A highly convergent synthetic approach was developed to obtain α- galactosyl cerebroside O-(α-D-galactopyranosyl)-2-hexacosylamino-D-ribo- 1,3,4-octadecantriol, which has previously been demonstrated to have immunostimulatory activity. Known 4,6-O-benzyli