159420-94-7

Basic information

• Product Name: 2,3,4-Tri-O-benzyl-β-D-glucopyranosiduronic Acid Benzyl Ester, Trichloroacetimidate
• Synonyms: 2,3,4-Tris-O-(phenylMethyl)-D-glucopyranuronic Acid PhenylMethyl Ester, 2,2,2-TrichloroethaniMidate;2,3,4-Tri-O-benzyl-β-D-glucopyranosiduronic Acid Benzyl Ester, Trichloroacetimidate
• CAS NO: 159420-94-7
• Molecular Formula: C36H34Cl3NO7
• Molecular Weight: 699.01666
• Product Categories: Carbohydrates & Derivatives
• Mol File: 159420-94-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer, Under Inert Atmosphere
• Solubility: Chloroform, Methanol
• CAS DataBase Reference: 2,3,4-Tri-O-benzyl-β-D-glucopyranosiduronic Acid Benzyl Ester, Trichloroacetimidate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4-Tri-O-benzyl-β-D-glucopyranosiduronic Acid Benzyl Ester, Trichloroacetimidate(159420-94-7)
• EPA Substance Registry System: 2,3,4-Tri-O-benzyl-β-D-glucopyranosiduronic Acid Benzyl Ester, Trichloroacetimidate(159420-94-7)

Safety Data

• Hazardous Substances Data: 159420-94-7(Hazardous Substances Data)

Usage

Chemical Properties

Pale Yellow Thick Oil

Uses

This compound is generally an alpha/beta mixture.

Upstream product

• 4539-78-0 2,3,4-tri-O-benzyl-D-glucopyranosideuronic acid benzyl ester 
• 545-06-2 trichloroacetonitrile 

Downstream Products

• 1607445-05-5 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose 
• 1607444-93-8 [benzyl (2,3,4-tri-O-benzyl-β-D-glucopyranosyl)uronate]-(1→ 2)-1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-β-D-mannopyranose 
• 1607444-94-9 [benzyl (2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]-(1→ 2)-1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-β-D-mannopyranose 
• 1599469-73-4 C₆₉H₆₂O₁₄ 
• 41945-43-1 (+)-Naproxen glucuronide 

Relevant articles and documents

Identification of the positional isomers of 2-fluorobenzoic acid 1-O-acyl glucuronide by directly coupled HPLC-NMR

Directly coupled HPLC-1H NMR was used in the "stop-flow" mode to separate and rapidly identify an equilibrated mixture of ester glucuronide isomers formed spontaneously by intramolecular rearrangement reactions (internal acyl migration and muta

Stereoselective synthesis of regioisomers of aldobiouronic acid

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