107242-80-8

Basic information

• Product Name: 1-O-allyl-6-O-trityl-α-D-glucopyranoside
• Synonyms: 1-O-allyl-6-O-trityl-α-D-glucopyranoside
• CAS NO: 107242-80-8
• Molecular Weight: 462.543
• Mol File: 107242-80-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-O-allyl-6-O-trityl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-allyl-6-O-trityl-α-D-glucopyranoside(107242-80-8)
• EPA Substance Registry System: 1-O-allyl-6-O-trityl-α-D-glucopyranoside(107242-80-8)

Safety Data

• Hazardous Substances Data: 107242-80-8(Hazardous Substances Data)

Upstream product

• 76-83-5 trityl chloride 
• 48149-74-2 allyl D-glucopyranoside 
• 2280-44-6 D-Glucose 
• 7732-18-5 water 
• 7464-56-4 1-O-allyl-α-D-glucopyranoside 

Downstream Products

• 340964-46-7 allyl 3,4-di-O-benzoyl-α-D-glucopyranoside 
• 340964-33-2 allyl 3,4-di-O-benzoyl-2-O-tert-butyldimethylsilyl-6-O-triphenylmethyl-α-D-glucopyranoside 
• 340964-54-7 allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1->6)-3,4-di-O-benzoyl-α-D-glucopyranoside 
• 155786-55-3 allyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4,6,7-penta-O-acetyl-L-glycero-α-D-manno-heptopyranosyl)-α-D-glucopyranoside 
• 168608-17-1 allyl 2,3,4-tri-O-benzyl-6-O-trityl-α-D-glucopyranoside 
• 168319-51-5 2,2,2-Trichloro-acetimidic acid (2S,3S,4R,5R,6S)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yl ester 
• 168319-48-0 (2S,3S,4S,5R,6S)-6-Allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid tert-butyl ester 
• 168319-49-1 Allyl(5R)-5-acetoxy-2,3,4-tri-O-benzyl-α-D-xylopyranoside 
• 168319-50-4 Allyl(5S)-5-hydroxy-2,3,4-tri-O-benzyl-α-D-xylopyranoside 
• 125426-22-4 (allyl 2,3,4-tri-O-benzyl-α-D-glucopyranosid)uronic acid 
• 78184-40-4 1-O-allyl-2,3,4-tri-O-benzyl-α-D-glucopyranoside 

Relevant articles and documents

Probing myo-inositol 1-phosphate synthase with multisubstrate adducts

The synthesis of a series of carbohydrate-nucleotide hybrids, designed to be multisubstrate adducts mimicking myo-inositol 1-phosphate synthase first oxidative transition state, is reported. Their ability to inhibit the synthase has been assessed and resu

Prodrugs for enzyme mediated activation

Enzymatically clearable prodrugs with reduced Michaelis-Menten constant (Km) are described.

Synthesis of linear oligosaccharides: L-glycero-α-D-manno-heptopyranosyl derivatives of allyl α-glycosides of D-glucose, kojibiose, and 3-O-α-kojibiosyl-D-glucose, substrates for synthetic antigens

Synthesis of the title oligosaccharides was performed with the use of peracetylated L-glycero-β-D-manno-heptosyl trichloroacetamidate as the heptosyl donor and (oligo)glucosyl acceptors bearing acyl and acetal protecting groups.