1415218-05-1

Basic information

• Product Name: p-tolyl 2,3-di-O-benzoyl-4-benzyl-1-thio-β-D-xylopyranose
• Synonyms: p-tolyl 2,3-di-O-benzoyl-4-benzyl-1-thio-β-D-xylopyranose
• CAS NO: 1415218-05-1
• Molecular Weight: 554.664
• Mol File: 1415218-05-1.mol

Chemical Properties

• CAS DataBase Reference: p-tolyl 2,3-di-O-benzoyl-4-benzyl-1-thio-β-D-xylopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: p-tolyl 2,3-di-O-benzoyl-4-benzyl-1-thio-β-D-xylopyranose(1415218-05-1)
• EPA Substance Registry System: p-tolyl 2,3-di-O-benzoyl-4-benzyl-1-thio-β-D-xylopyranose(1415218-05-1)

Safety Data

• Hazardous Substances Data: 1415218-05-1(Hazardous Substances Data)

Upstream product

• 1269466-59-2 p-methylphenyl 4-O-benzyl-1-thio-β-D-xylopyranoside 
• 98-88-4 benzoyl chloride 
• 1415218-04-0 p-tolyl 2,3-isopropylidene-4-benzyl-1-thio-β-D-xylopyranose 
• 1415218-00-6 1-(4-tolyl)thio-2,3-O-isopropylidene-β-D-xylopyranoside 
• 67803-94-5 4-methylphenyl 1-thio-β-D-xylopyranoside 
• 61025-08-9 p-methylphenyl 2,3,4-tri-O-acetyl-1-thio-β-D-xylopyranoside 

Downstream Products

• 1415218-09-5 4-methylphenyl 2,3-di-O-benzoyl-1-thio-β-D-xylopyranoside 
• 1426447-50-8 p-tolyl 2,3-di-O-benzoyl-4-O-tert-butyldimethylsilyl-1-thio-β-D-xylopyranoside 
• 1415218-12-0 N-fluorenylmethyloxycarbonyl-O-(2,3-di-O-benzoyl-4-O-tert-butyldimethylsilyl-β-D-xylopyranosyl)-L-serine benzyl ester 
• 1415218-13-1 N-fluorenylmethyloxycarbonyl-O-(2,3-di-O-benzoyl-β-D-xylopyranosyl)-L-serine benzyl ester 
• 1415218-10-8 N-fluorenylmethyloxycarbonyl-O-(2,3-di-O-benzoyl-4-O-benzyl-β-D-xylopyranosyl)-L-serine benzyl ester 

Relevant articles and documents

Chemical synthesis of a heparan sulfate glycopeptide: Syndecan-1

Finishing first: The highly complex structure of the title compound (see picture) was assembled. The protective groups utilized, as well as the sequences for formation of the glycosyl linkages and protecting group removal are critical to the success of the synthesis. This first preparation of a heparan sulfate glycopeptide lays the foundation for accessing other members of this class of molecules. Copyright