7473-44-1

Basic information

• Product Name: β-L-Arabinopyranose tetrabenzoate
• Synonyms: β-L-Arabinopyranose tetrabenzoate;Nsc400283
• CAS NO: 7473-44-1
• Molecular Formula: C₃₃H₂₆O₉
• Molecular Weight: 566.5541
• Mol File: 7473-44-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 702.1°Cat760mmHg
• Flash Point: 294°C
• Appearance: /
• Density: 1.36g/cm³
• Vapor Pressure: 1.46E-19mmHg at 25°C
• Refractive Index: 1.639
• CAS DataBase Reference: β-L-Arabinopyranose tetrabenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: β-L-Arabinopyranose tetrabenzoate(7473-44-1)
• EPA Substance Registry System: β-L-Arabinopyranose tetrabenzoate(7473-44-1)

Safety Data

• Hazardous Substances Data: 7473-44-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C33H26O9/c34-29(22-13-5-1-6-14-22)39-26-21-38-33(42-32(37)25-19-11-4-12-20-25)28(41-31(36)24-17-9-3-10-18-24)27(26)40-30(35)23-15-7-2-8-16-23/h1-20,26-28,33H,21H2

Upstream product

• 87-72-9 L-xylopyranose 
• 98-88-4 benzoyl chloride 
• 609-06-3 L-xylose 
• 5328-37-0 L-arabinose 
• 30319-42-7 1,2,3,4-tetra-O-benzoyl-α-D-arabinopyranose 
• 1087699-39-5 1,2,3,4-tetra-O-benzoyl-α-L-arabinopyranose 
• 22434-99-7 1,2,3,4-tetra-O-benzoyl-β-D-arabinopyranose 
• 20235-19-2 arabinose 

Downstream Products

• 1207607-96-2 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl bromide 
• 7473-43-0 tetra-O-benzoyl-β-DL-arabinopyranose 
• 15356-05-5 N,N'-L-arabitol-1-ylidene-bis-benzamide 
• 202401-18-1 methyl 2,3,4-tri-O-benzoyl-α-L-arabinopyranoside 
• 73347-39-4 tri-O-benzoyl-1,5-anhydro-L_g-threo-pent-1-enitol 
• 125572-77-2 2-phenylethyl 1-O-α-L-arabinopyranosyl-(1->6)-β-D-glucopyranoside 
• 192827-22-8 geranyl 2,3,4,2',3',4'-O-hexabenzoyl-α-L-arabinopyranosyl-(1->6)-β-D-glucopyranoside 
• 192827-23-9 C₆₃H₆₀O₁₆ 
• 192827-20-6 C₆₀H₅₀O₁₆ 
• 152520-94-0 geraniol-1-O-α-L-arabinopyranosyl-(1->6)-β-D-glucopyranoside 
• 14206-56-5 2,3,4-tri-O-benzoyl-β-L-arabinopyranosyl bromide 

Relevant articles and documents

Synthesis of a Tridecasaccharide Lipooligosaccharide Antigen from the Opportunistic Pathogen Mycobacterium kansasii

The outer surfaces of mycobacteria, including the organism that causes tuberculosis, are decorated with an array of immunomodulatory glycans. Among these are lipooligosaccharides (LOSs), a class of molecules for which the function remains poorly understoo

Synthesis of two natural betulinic acid saponins containing α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranose and their analogues

A concise synthesis of naturally occurring betulinic acid saponins bearing an α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranoside moiety at the C-3 position is described. Betulinic acid 3β-O-α-l-rhamnopyranosyl-(1→2)-[β-d-glucopyranosyl- (1→4)]-α-l-arabinopyr