10238-27-4

Usage

Uses

Used in Organic Synthesis:
2-NITROPHENYL-BETA-D-XYLOPYRANOSIDE is used as a synthetic building block for the creation of various complex organic molecules. Its unique structure allows chemists to manipulate and modify it to synthesize a wide range of compounds with specific properties and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-NITROPHENYL-BETA-D-XYLOPYRANOSIDE is used as a key intermediate in the synthesis of drugs targeting specific biological pathways. Its structural diversity and compatibility with various functional groups make it a valuable component in the development of novel therapeutic agents.
Used in Chemical Research:
2-NITROPHENYL-BETA-D-XYLOPYRANOSIDE is also employed as a research tool in chemical laboratories. Its unique properties and reactivity enable scientists to study various chemical reactions and mechanisms, contributing to the advancement of chemical knowledge and the development of new synthetic strategies.
Used in Material Science:
In the field of material science, 2-NITROPHENYL-BETA-D-XYLOPYRANOSIDE can be used as a component in the development of novel materials with specific properties, such as improved mechanical strength, thermal stability, or biocompatibility. Its incorporation into polymers or other materials can lead to the creation of innovative products with enhanced performance characteristics.

InChI:InChI=1/C11H13NO7/c13-7-5-18-11(10(15)9(7)14)19-8-4-2-1-3-6(8)12(16)17/h1-4,7,9-11,13-15H,5H2/t7-,9+,10-,11+/m1/s1

Upstream product

• 10256-24-3 o-nitrophenyl 2,3,4,6-tetra-O-acetyl-β-D-xylopyranoside 
• 88-75-5 2-hydroxynitrobenzene 
• 3068-31-3 1-bromo-2,3,4-tri-O-acetyl-α-D-xylopyranose 

Downstream Products

• 173468-05-8 2-nitrophenyl 4-O-chloroacetyl-β-D-xylopyranoside 
• 88-75-5 2-hydroxynitrobenzene 
• 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 
• 173468-07-0 2-nitrophenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-β-D-xylopyranoside 
• 173468-28-5 2-nitrophenyl O-β-D-xylopyranosyl-(1<*>4)-O-β-D-xylopyranosyl-(1<*>4)-β-D-xylopyranoside 
• 173468-34-3 2-nitrophenyl O-β-D-xylopyranosyl-(1<*>4)-bis4)>-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 
• 173468-24-1 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 
• 173468-30-9 2-nitrophenyl O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-(1<*>4)-bis4)>-2,3-di-O-benzoyl-β-D-xylopyranoside 
• 162088-91-7 2'-nitrophenyl 2,3-di-O-acetyl-β-D-xylopyranoside 
• 162088-90-6 2'-nitrophenyl 2,3-di-O-acetyl-4-O-triethylsilyl-β-D-xylopyranoside 
• 162088-92-8 2-nitrophenyl O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-(1<*>4)-2,3-di-O-acetyl-β-D-xylopyranoside 
• 2460-44-8 β-D-xylopyranoside 

Relevant academic research and scientific papers

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.