2595-41-7

Basic information

• Product Name: 2,3,4-tri-O-acetyl-1-S-carbamimidoyl-1-thiopentopyranose
• CAS NO: 2595-41-7
• Molecular Formula: BrH*C₁₂H₁₈N₂O₇S
• Molecular Weight: 334.3455
• Mol File: 2595-41-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 425.1°C at 760 mmHg
• Flash Point: 210.9°C
• Density: 1.51g/cm³
• Vapor Pressure: 1.96E-07mmHg at 25°C
• Refractive Index: 1.59
• CAS DataBase Reference: 2,3,4-tri-O-acetyl-1-S-carbamimidoyl-1-thiopentopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4-tri-O-acetyl-1-S-carbamimidoyl-1-thiopentopyranose(2595-41-7)
• EPA Substance Registry System: 2,3,4-tri-O-acetyl-1-S-carbamimidoyl-1-thiopentopyranose(2595-41-7)

Safety Data

• Hazardous Substances Data: 2595-41-7(Hazardous Substances Data)

Upstream product

• 3068-31-3 2,3,4-tri-O-acetyl-α-D-xylopyranosyl bromide 
• 17356-08-0 thiourea 
• 3068-31-3 1-bromo-2,3,4-tri-O-acetyl-α-D-xylopyranose 

Downstream Products

• 359407-47-9 C₅₀H₅₀O₁₈S₂ 
• 359407-45-7 C₃₁H₃₄O₁₃S 
• 82040-50-4 1,2,3-tri-O-benzoyl-4-S-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-4-thio-α-D-xylopyranose 
• 77164-46-6 p-nitrophenyl 2,3,4-tri-O-acetyl-1-thio-β-D-xylopyranoside 

Relevant articles and documents

S -Glycosides: Synthesis of S -linked arabinoxylan oligosaccharides

S-Glycosides are important tools for the elucidation of specific protein-carbohydrate interactions and can significantly aid structural and functional studies of carbohydrate-active enzymes, as they are often inert or act as enzyme inhibitors. In this con

Stereoselective synthesis of thioxylooligosaccharides from S-glycosyl isothiourea precursors

A stereoselective synthesis of thioxylo-di-, -tri-, -tetra- and -penta-saccharides from S-glycosyl isothiourea precursors is described. The synthesis was performed starting from 2,3,4-tri-O-acetyl-β-D-xylopyranosyl isothiouronium bromide using a triethylamine promoted reaction with 1,2,3-tri-O-benzoyl-4-O-trifluoromethanesulphonyl-β-L-arabinopyranose. The resulting 4-thioxylobiose was then converted into the corresponding isothiouronium bromide and used for the synthesis of 4,4′-dithioxylotriose. Higher homologues of the series and their α-methyl glycosides were also prepared.