85820-98-0

Upstream product

• 163668-94-8 1-O-allyl-2-O-benzyl-3-O-triphenylmethylglycerol 
• 95870-54-5 1-O-allyl-3-O-triphenylmethylglycerol 

Downstream Products

• 163668-85-7 1-O-allyl-2-O-benzyl-3-O-trifluoromethanesulfonylglycerol 
• 163668-87-9 methyl 3,4,6-tri-O-benzyl-2-O-(2-benzyloxy-3-hydrtoxypropyl)-α-D-glucopyranoside 
• 163668-86-8 methyl 2-O-(3-allyloxy-2-benzyloxypropyl)-3,4,6-tri-O-benzyl-α-D-glucopyranoside 
• 163668-91-5 methyl 3,4,6-tri-O-benzyl-2-O-(2-benzyloxy-6,7-epoxy-4-oxaheptyl)-α-D-glucopyranoside 
• 163668-92-6 methyl 3,4,6-tri-O-benzyl-2-O-(2-benzyloxy-6,7-dihydroxy-4-oxaheptyl)-α-D-glucopyranoside 
• 163668-93-7 2-benzyloxy-1,3-bis(methyl 3,4,6-tri-O-benzyl-α-D-glucopyranosid-2-O-yl)propane 

Relevant academic research and scientific papers

The reaction between epichlorohydrin and polysaccharides: Part 1, syntheses of some model substances with non-cyclic substituents

Five derivatives of methyl α-D-glucopyranoside, in which the substituents form noncyclic structures, have been prepared as model substances for possible structural elements formed on reaction of polysaccharides with epichlorohydrin.The substances were converted into the permethylated alditol-1-d derivatives and characterised by CIMS and EIMS.