869201-28-5

Basic information

• Product Name: allyl 3,6-di-O-benzyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranoside
• Synonyms: allyl 3,6-di-O-benzyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranoside
• CAS NO: 869201-28-5
• Molecular Weight: 574.886
• Mol File: 869201-28-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: allyl 3,6-di-O-benzyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 3,6-di-O-benzyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranoside(869201-28-5)
• EPA Substance Registry System: allyl 3,6-di-O-benzyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranoside(869201-28-5)

Safety Data

• Hazardous Substances Data: 869201-28-5(Hazardous Substances Data)

Upstream product

• 287922-84-3 allyl 3-O-benzyl-4,6-O-benzylidene-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside 

Downstream Products

• 1179813-95-6 allyl 4-O-[3-O-(4-azido-3-chlorobenzyl)-4,6-O-benzylidene-2-O-benzyl-β-D-mannopyranosyl]-3,6-di-O-benzyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside 
• 1186302-38-4 allyl 3,6-di-O-benzyl-4-O-9-fluorenylmethyloxycarbonyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside 
• 1025449-58-4 allyl-3,6-di-O-benzyl-4-O-(dibenzyloxyphosphoryl)-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside 
• 1262956-57-9 C₄₉H₅₂Cl₆N₂O₁₃ 

Relevant articles and documents

Efficient procedure for reductive opening of sugar 4,6-O-benzylidene acetals in a microfluidic system

An efficient procedure for the reductive opening of 4,6-O-benzylidene acetals was established under microfluidic conditions. 4,6-O-Benzylidene acetals of the glucose, glucosamine, and galactose derivatives were selectively converted into the corresponding

Towards glucosamine building blocks: Regioselective one-pot protection and deallylation procedures

Glucosamine building blocks have been prepared by an efficient regioselective one-pot protection approach. This synthetic route enabled the straightforward preparation of a glucosamine disaccharide in 73% yield. The system Pd(PPh3)4/