76303-17-8

Basic information

• Product Name: methyl 2-O-benzoyl-4,6-O-benzylidene-3-O-selenobenzoyl-α-D-glucopyranoside
• CAS NO: 76303-17-8
• Molecular Weight: 553.47
• Mol File: 76303-17-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-O-benzoyl-4,6-O-benzylidene-3-O-selenobenzoyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-O-benzoyl-4,6-O-benzylidene-3-O-selenobenzoyl-α-D-glucopyranoside(76303-17-8)
• EPA Substance Registry System: methyl 2-O-benzoyl-4,6-O-benzylidene-3-O-selenobenzoyl-α-D-glucopyranoside(76303-17-8)

Safety Data

• Hazardous Substances Data: 76303-17-8(Hazardous Substances Data)

Upstream product

• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 2397-26-4 N,N-dimethyl(chlorophenylmethylene)ammonium chloride 
• 64713-83-3 methyl 4,6-O-benzylidene-3-O-selenobenzoyl-α-D-glucopyranoside 
• 98-88-4 benzoyl chloride 
• 611-74-5 N,N-dimethylbenzamide 

Relevant articles and documents

Reactions of Relevance to the Chemistry of Aminoglycoside Antibiotics. Part 13. A Novel Synthesis of Benzyl Ethers

Benzyl ethers were prepared from alcohols by reaction with chloro(phenylmethyl)dimethylammonium chloride and sodium hydrogen telluride in sequence.The salt (1) 1)OR2Cl-; R1=H, R2=cholest-5-en-3β-yl> and sodium borohydride gave the borane complex of 3β-dimethylaminomethoxycholest-5-ene.Salt (1; R1=Ph, R2=cholest-5-en-3β-yl or 5α-cholestan-3β-yl) and ammonia or hydrazine gave the steroidal benzimidates or benzhydrazonate.