95722-13-7

Basic information

• Product Name: 1,2,3,4-tetra-O-acetyl-α-D-galactopyranosiduronic acid
• CAS NO: 95722-13-7
• Molecular Weight: 362.29
• Mol File: 95722-13-7.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 1,2,3,4-tetra-O-acetyl-α-D-galactopyranosiduronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-tetra-O-acetyl-α-D-galactopyranosiduronic acid(95722-13-7)
• EPA Substance Registry System: 1,2,3,4-tetra-O-acetyl-α-D-galactopyranosiduronic acid(95722-13-7)

Safety Data

• Hazardous Substances Data: 95722-13-7(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 14984-34-0 sodium D-glucuronate 
• 104-15-4 toluene-4-sulfonic acid 
• 6556-12-3 D-glucuronic acid 
• 489-91-8 D-glucuronic acid 
• 474426-72-7 acetic 1,2,3,4-tetra-O-acetyl-β-D-glucopyranuronic anhydride 
• 24016-65-7 D-glucuronic acid sodium salt 
• 18281-92-0 β-D-glucurono-6,3-lactone 

Downstream Products

• 7355-18-2 (2S,3S,4S,5R,6S)-3,4,5,6-Tetraacetoxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 499-05-8 comanic acid 
• 110454-51-8 (2S,3R,4S)-2,3,4-triacetoxy-3,4-dihydro-2H-pyran-6-carboxylic acid 
• 474426-79-4 Acetic acid (2S,3S,4S,5R,6S)-4,5,6-triacetoxy-2-phenylcarbamoyl-tetrahydro-pyran-3-yl ester 
• 474426-82-9 1,2,3,4-tetra-O-acetyl-β-D-glucopyranuron-N-methyl-N-phenylamide 
• 1345853-98-6 N-(2-chloro-4-nitrophenyl)-1,2,3-tri-O-acetyl-Δ4,5-β-D-glucopyranuronamide 
• 1345854-00-3 N-(2-chloro-4-nitrophenyl)-1,2,3,4-tetra-O-acetyl-β-D-glucopyranuronamide 
• 4310-12-7 1,2,3,4-tetra-O-acetyl-N-benzyl-β-D-glucopyranuronamide 
• 1345853-88-4 N-benzyl-1,2,3-tri-O-acetyl-Δ4,5-β-D-glucopyranuronamide 
• 1345853-94-2 N-(4-bromophenyl)-1,2,3-tri-O-acetyl-Δ4,5-β-D-glucopyranuronamide 
• 1345853-96-4 N-(4-bromophenyl)-1,2,3,4-tetra-O-acetyl-β-D-glucopyranuronamide 
• 10344-94-2 p-nitrophenyl-β-D-glucuronide 
• 34351-67-2 p-methoxybenzyl-2,3,4-tri-O-acetyl-beta-D-glucuronic acid methyl ester 
• 18472-49-6 methyl <4'-nitrophenyl 2,3,4-tri-O-acetyl-β-D-glucopyranosid>uronate 

Relevant articles and documents

Synthesis and structural analysis of the anilides of glucuronic acid and orientation of the groups on the carbohydrate scaffolding

The synthesis of anilides derived from glucuronic acid is described. Secondary anilides had a Z configuration in the solid state and showed intramolecular and intermolecular hydrogen bonding. However, on the basis of NMR and IR studies, there was generall

Preparation method of substituted benzyl or substituted phenyl beta-D-hexuronic acid glucoside

The invention relates to the technical field of pharmaceutical and chemical industries, and discloses a preparation method of substituted benzyl or substituted phenyl beta-D-hexuronic acid glucoside.The preparation method comprises the steps of taking hexuronic acid as a raw material, and performing acetylation, selective acyl removal, methyl esterification, bromization, aethrization and alkalinealcoholysis to form substituted benzyl or substituted phenyl beta-hexuronic acid glucoside with a structural formula as follows as shown in the description, wherein n is equal to 0-1; and R is o-, m-or para-hydrogen, nitryl, methoxy or halogen. The method is mild in reaction condition, simple in step and suitable for large-scale preparation, and a reaction reagent is easy to obtain.

Sweet anion receptors: Recognition of chiral carboxylate anions by d-glucuronic-acid-decorated diindolylmethane

Anion receptors containing glucuronic acid were synthesized, and their anion binding ability studied. Chirality of anionic guests derived from mandelic acid and amino acids can be distinguished not only in terms of stability constants but also by signific