1235973-11-1

Basic information

• Product Name: allyl 3-O-(4-azido-3-chlorobenzyl)-4,6-O-benzylidene-α-D-mannopyranoside
• Synonyms: allyl 3-O-(4-azido-3-chlorobenzyl)-4,6-O-benzylidene-α-D-mannopyranoside
• CAS NO: 1235973-11-1
• Molecular Weight: 473.913
• Mol File: 1235973-11-1.mol

Chemical Properties

• CAS DataBase Reference: allyl 3-O-(4-azido-3-chlorobenzyl)-4,6-O-benzylidene-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 3-O-(4-azido-3-chlorobenzyl)-4,6-O-benzylidene-α-D-mannopyranoside(1235973-11-1)
• EPA Substance Registry System: allyl 3-O-(4-azido-3-chlorobenzyl)-4,6-O-benzylidene-α-D-mannopyranoside(1235973-11-1)

Safety Data

• Hazardous Substances Data: 1235973-11-1(Hazardous Substances Data)

Upstream product

• 81600-93-3 allyl 4,6-di-O-benzylidene-α-D-mannopyranoside 
• 193887-70-6 4-azido-3-chlorobenzyl bromide 

Downstream Products

• 1186302-51-1 allyl 3-O-(4-azido-3-chlorobenzyl)-4,6-O-benzylidene-2-O-benzyl-α-D-mannopyranoside 

Relevant articles and documents

Synthesis of a sialic acid containing complex-type n-glycan on a solid support

A new solid-phase synthesis of N-linked glycans featuring 1) highly ste-reoselective b-mannosylation and microfluidic a-sialylation and 2) efficient glycosylation of the N-phenyltrifluoroacetimidate units on JandaJel resin is reported. Reagent concentration effects by a fluorous solvent are effectively applied, and the use of these methods results in the first synthesis of a sialic acid containing complex-type N-glycan on a solid support.