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3-phenoxybenzyl beta-D-glucopyranosiduronic acid

Base Information
  • Chemical Name:3-phenoxybenzyl beta-D-glucopyranosiduronic acid
  • CAS No.:65658-93-7
  • Molecular Formula:C19H20 O8
  • Molecular Weight:376.3573
  • Hs Code.:
3-phenoxybenzyl beta-D-glucopyranosiduronic acid

Synonyms:

Suppliers and Price of 3-phenoxybenzyl beta-D-glucopyranosiduronic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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  • price
Total 1 raw suppliers
Chemical Property of 3-phenoxybenzyl beta-D-glucopyranosiduronic acid
Chemical Property:
  • Vapor Pressure:5.28E-16mmHg at 25°C 
  • Boiling Point:615.4°C at 760 mmHg 
  • Flash Point:221.6°C 
  • Density:1.48g/cm3 
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 3-phenoxybenzyl beta-D-glucopyranosiduronic acid

There total 2 articles about 3-phenoxybenzyl beta-D-glucopyranosiduronic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
methyl 2,3,4-tri-O-acetyl-1-(3-phenoxybenzyl)-β-D-glucopyranouronate; With sodium methylate; In methanol; at 20 ℃; for 24h;
With barium dihydroxide; In methanol; at 20 ℃; for 24h; Further stages.;
DOI:10.1021/jf063282g
Guidance literature:
Multi-step reaction with 3 steps
1.1: 76 percent / hydrobromic acid / CH2Cl2; acetic acid / 3 h / 20 °C
2.1: 55 percent / silver trifluoromethanesulfonate; tetramethylurea / CH2Cl2 / 12 h / -20 °C
3.1: sodium methoxide / methanol / 24 h / 20 °C
3.2: 40 percent / Ba(OH)2 / methanol / 24 h / 20 °C
With hydrogen bromide; sodium methylate; silver trifluoromethanesulfonate; tetramethylurea; In methanol; dichloromethane; acetic acid; 2.1: Koenigs-Knorr reaction;
DOI:10.1021/jf063282g
Guidance literature:
1-(3-phenoxybenzyl)-β-D-glucuronide; With 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 4 ℃;
[3-(2-aminoethyl)dithio]propionic acid hydrochloride; With triethylamine; In N,N-dimethyl-formamide; at 4 ℃; Further stages.;
DOI:10.1021/jf063282g
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