236743-96-7

Basic information

• Product Name: (S)-1-(O-benzyl-N-tert-butoxycarbonyl-L-threonine)-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)propane
• Synonyms: (S)-1-(O-benzyl-N-tert-butoxycarbonyl-L-threonine)-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)propane
• CAS NO: 236743-96-7
• Molecular Weight: 887.126
• Mol File: 236743-96-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-1-(O-benzyl-N-tert-butoxycarbonyl-L-threonine)-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)propane(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(O-benzyl-N-tert-butoxycarbonyl-L-threonine)-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)propane(236743-96-7)
• EPA Substance Registry System: (S)-1-(O-benzyl-N-tert-butoxycarbonyl-L-threonine)-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)propane(236743-96-7)

Safety Data

• Hazardous Substances Data: 236743-96-7(Hazardous Substances Data)

Upstream product

• 236743-75-2 (S)-1-azido-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)propane 
• 236743-61-6 (S)-1-azido-3-(tri-O-benzyl-α-L-fucopyranosyl)-2-propanol 
• 236743-51-4 1,2-epoxy-3-(tri-O-benzyl-α-L-fucopyranosyl)-propane 
• 167990-42-3 3-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-1-propene 
• 15260-10-3 N-Boc-O-benzyl-L-threonine 
• 236743-87-6 (S)-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)-1-propyl amine 

Downstream Products

• 204458-74-2 (S)-1-(O-benzyl-2-monobenzylsuccinimidyl-L-threonine)-2-(2-phenethoxy)-3-(tri-O-benzyl-α-L-fucopyranosyl)propane 

Relevant articles and documents

Design, synthesis and biological evaluation of aryl-substituted sialyl Lewis X mimetics prepared via cross-metathesis of C-fucopeptides

Several aryl substituted C-fucopeptides have been developed as sialyl Lewis X mimetics. Although the compounds have a much simpler structure compared to SLe(x), up to 3-times higher binding affinity toward E-selectin and >1000 times toward P-selectin was observed. Furthermore, a convenient strategy for generating a number of analogues from a SLe(x) mimetic template at a very late stage of the synthesis was introduced, using a ruthenium catalyzed cross olefin metathesis under benchtop conditions. Copyright (C) 1999 Elsevier Science Ltd.