173468-07-0

Basic information

• Product Name: 2-nitrophenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-β-D-xylopyranoside
• Synonyms: 2-nitrophenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-β-D-xylopyranoside
• CAS NO: 173468-07-0
• Molecular Weight: 555.925
• Mol File: 173468-07-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-nitrophenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-β-D-xylopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-nitrophenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-β-D-xylopyranoside(173468-07-0)
• EPA Substance Registry System: 2-nitrophenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-β-D-xylopyranoside(173468-07-0)

Safety Data

• Hazardous Substances Data: 173468-07-0(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 173468-05-8 2-nitrophenyl 4-O-chloroacetyl-β-D-xylopyranoside 
• 3068-31-3 1-bromo-2,3,4-tri-O-acetyl-α-D-xylopyranose 
• 88-75-5 2-hydroxynitrobenzene 
• 10256-24-3 o-nitrophenyl 2,3,4,6-tetra-O-acetyl-β-D-xylopyranoside 
• 10238-27-4 2-nitrophenyl β-D-xylopyranoside 

Downstream Products

• 173468-30-9 2-nitrophenyl O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-(1<*>4)-bis4)>-2,3-di-O-benzoyl-β-D-xylopyranoside 
• 173468-24-1 2-nitrophenyl O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-(1<*>4)-O-(2,3-di-O-acetyl-β-D-xylopyranosyl)-(1<*>4)-2,3-di-O-benzoyl-β-D-xylopyranoside 
• 173468-13-8 2-nitrophenyl O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-(1<*>4)-2,3-di-O-benzoyl-β-D-xylopyranoside 
• 173468-34-3 2-nitrophenyl O-β-D-xylopyranosyl-(1<*>4)-bis4)>-β-D-xylopyranoside 
• 173468-28-5 2-nitrophenyl O-β-D-xylopyranosyl-(1<*>4)-O-β-D-xylopyranosyl-(1<*>4)-β-D-xylopyranoside 
• 157956-98-4 2-nitrophenyl O-β-D-xylopyranosyl-(1<*>4)-β-D-xylopyranoside 
• 173468-08-1 2-nitrophenyl 2,3-di-O-benzoyl-β-D-xylopyranoside 

Relevant articles and documents

Synthesis of 2- and 4-nitrophenyl β-glycosides of β-(1 → 4)-D-xylo-oligosaccharides of dp 2-4

2- and 4-Nitrophenyl β-D-xylopyranosides (4 and 5) were transformed, via dibutyltin oxide-mediated acylation, into the corresponding 2,3-di-O-benzoyl derivatives 11 and 15. Xylobiose and xylotriose were easily isolated by charcoal column chromatography from a commercially available material and converted into the di- and trisaccharide methyl 1-thio-β-glycosides 36 and 37. The 2- and 4-nitrophenyl β-glycosides of the β-(1 → 4)-D-xylo-oligosaccharides of dp 2-4 were synthesized by N-iodosuccinimide-silver triflate-promoted condensation using 11 and 15 as the glycosyl acceptors and ethyl 1-thio-β-D-xylopyranoside triacetate 16, 36, and 37 as the glycosyl donors. Also described are an improved preparation of 4 and 5, and the synthesis of 1-naphthyl β-D-xylopyranoside, as well as an alternative approach to the 2- and 4-nitrophenyl β-xylobiosides.