1252027-51-2

Basic information

• Product Name: (2-acetamido-3,4-di-O-benzyl-6-O-chloroacetyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-[tert-butyl (2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-N-(4-nitro)benzenesulfonyl-L-iditol)uronate]
• Synonyms: (2-acetamido-3,4-di-O-benzyl-6-O-chloroacetyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-[tert-butyl (2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-N-(4-nitro)benzenesulfonyl-L-iditol)uronate]
• CAS NO: 1252027-51-2
• Molecular Weight: 1058.6
• Mol File: 1252027-51-2.mol

Chemical Properties

• CAS DataBase Reference: (2-acetamido-3,4-di-O-benzyl-6-O-chloroacetyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-[tert-butyl (2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-N-(4-nitro)benzenesulfonyl-L-iditol)uronate](CAS DataBase Reference)
• NIST Chemistry Reference: (2-acetamido-3,4-di-O-benzyl-6-O-chloroacetyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-[tert-butyl (2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-N-(4-nitro)benzenesulfonyl-L-iditol)uronate](1252027-51-2)
• EPA Substance Registry System: (2-acetamido-3,4-di-O-benzyl-6-O-chloroacetyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-[tert-butyl (2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-N-(4-nitro)benzenesulfonyl-L-iditol)uronate](1252027-51-2)

Safety Data

• Hazardous Substances Data: 1252027-51-2(Hazardous Substances Data)

Upstream product

• 1207750-82-0 (2-azido-3,4-di-O-benzyl-2-deoxy-6-O-chloroacetyl-α-D-glucopyranosyl)-(1->4)-[tert-butyl [2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-N-(4-nitro)benzenesulfonyl-L-iditol]uronate] 
• 108-24-7 acetic anhydride 

Downstream Products

• 1252027-52-3 (2-acetamido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-[tert-butyl (2,3-di-O-benzyl-1,5-dideoxy-1,5-imino-N-(4-nitro)benzenesulfonyl-L-iditol)uronate] 

Relevant articles and documents

Synthesis of glycosaminoglycan oligosaccharides. Part 4: Synthesis of aza-l-iduronic acid-containing analogs of heparan sulfate oligosaccharides as heparanase inhibitors

The synthesis of three azasugar-containing analogs of the disaccharide units of heparan sulfate, which are potential inhibitors of the enzyme heparanase, is reported. Synthetic routes were developed for the preparation of l-ido-nojirimycin type glycosyl a