250330-71-3

Basic information

• Product Name: N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-cellobioside
• Synonyms: N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-cellobioside
• CAS NO: 250330-71-3
• Molecular Weight: 739.769
• Mol File: 250330-71-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-cellobioside(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-cellobioside(250330-71-3)
• EPA Substance Registry System: N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-cellobioside(250330-71-3)

Safety Data

• Hazardous Substances Data: 250330-71-3(Hazardous Substances Data)

Upstream product

• 37860-51-8 tetraethylene glycol di(p-toluenesulfonate) 
• 5328-50-7 D-cellobiose octaacetate 
• 112-60-7 Tetraethylene glycol 
• 669556-37-0 17-(tetrahydro-2H-pyran-2-yloxy)-3,6,9,12,15-pentaoxaheptadecyl 4-methylbenzenesulfonate 
• 250330-58-6 benzyl N-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate 
• 250330-69-9 4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α/β-D-glucopyranosyl trichloroacetimidate 
• 86770-69-6 17-azido-3,6,9,12,15-pentaoxaheptadecan-1-ol 
• 39160-70-8 3,6,9,12,15,18-hexaoxa-1-octadecyl amine 
• 18464-08-9 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-glucopyranose 
• 250330-70-2 N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 

Relevant articles and documents

Synthesis of heparin-like antithrombotics having perphosphorylated thrombin binding domains

The synthesis of three heparin analogues (i.e. compounds VI-VIII) having perphosphorylated thrombin binding domains (TBDs) is reported. These compounds were tested in vitro for their antithrombin III (ATIII)-mediated anti-Xa and antithrombin activities. Conjugates VI and VIII show a remarkable increase in antithrombin activity compared to the structurally related conjugates with persulfated TBDs (i.e. compounds IV and V), whereas compound VII displays a diminished activity.