270075-70-2

Basic information

• Product Name: 5-(methoxycarbonyl)pentyl 2-O-benzoyl-3-O-chloroacetyl-4-O-stearoyl-α-L-rhamnopyranoside
• Synonyms: 5-(methoxycarbonyl)pentyl 2-O-benzoyl-3-O-chloroacetyl-4-O-stearoyl-α-L-rhamnopyranoside
• CAS NO: 270075-70-2
• Molecular Weight: 739.387
• Mol File: 270075-70-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-(methoxycarbonyl)pentyl 2-O-benzoyl-3-O-chloroacetyl-4-O-stearoyl-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(methoxycarbonyl)pentyl 2-O-benzoyl-3-O-chloroacetyl-4-O-stearoyl-α-L-rhamnopyranoside(270075-70-2)
• EPA Substance Registry System: 5-(methoxycarbonyl)pentyl 2-O-benzoyl-3-O-chloroacetyl-4-O-stearoyl-α-L-rhamnopyranoside(270075-70-2)

Safety Data

• Hazardous Substances Data: 270075-70-2(Hazardous Substances Data)

Upstream product

• 270075-67-7 phenyl 2-O-benzoyl-3-O-chloroacetyl-4-O-stearoyl-1-thio-α-L-rhamnopyranoside 
• 270075-66-6 phenyl 2-O-benzoyl-4-O-stearoyl-1-thio-α-L-rhamnopyranoside 
• 270075-82-6 Octadecanoic acid (3aR,4S,6S,7S,7aR)-2,2,6-trimethyl-4-phenylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester 
• 270075-65-5 phenyl 4-O-stearoyl-1-thio-α-L-rhamnopyranoside 
• 707-07-3 orthobenzoic acid trimethyl ester 
• 131087-35-9 phenyl 2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside 
• 1214-98-8 phenyl 1-thio-α-L-rhamnopyranose 
• 4547-43-7 methyl 6-hydroxycaproate 
• 270075-69-9 2-O-benzoyl-3-O-chloroacetyl-4-O-stearoyl-L-rhamnopyranosyl trichloroacetimidate 

Downstream Products

• 270075-77-9 5-(methoxycarbonyl)pentyl (4,6-di-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-(1->3)-2-O-benzoyl-4-O-stearoyl-α-L-rhamnopyranoside 
• 270075-76-8 5-(methoxycarbonyl)pentyl (4,6-di-O-acetyl-2-azido-3-O-chloroacetyl-2-deoxy-α-D-glucopyranosyl)-(1->3)-2-O-benzoyl-4-O-stearoyl-α-L-rhamnopyranoside 
• 270075-71-3 5-(methoxycarbonyl)pentyl 2-O-benzoyl-4-O-stearoyl-α-L-rhamnopyranoside 

Relevant articles and documents

A new strategy in oligosaccharide synthesis using lipophilic protecting groups: synthesis of a tetracosasaccharide

The use of lipophilic, acyl-type protecting groups in the synthesis of higher-membered oligosaccharides is described by the example of oligosaccharides corresponding to the O-specific polysaccharide (O-SP) of Shigella dysenteriae type 1. Thus, O-stearoyla