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.beta.-D-Glucopyranuronic acid, 5-C-bromo-, methyl ester, tetraacetate

Base Information
  • Chemical Name:.beta.-D-Glucopyranuronic acid, 5-C-bromo-, methyl ester, tetraacetate
  • CAS No.:65615-69-2
  • Molecular Formula:C15H19BrO11
  • Molecular Weight:455.213
  • Hs Code.:
.beta.-D-Glucopyranuronic acid, 5-C-bromo-, methyl ester, tetraacetate

Synonyms:methyl (5R)-1,2,3,4-tetra-O-acetyl-5-C-bromo-β-D-glucopyranuronate

Suppliers and Price of .beta.-D-Glucopyranuronic acid, 5-C-bromo-, methyl ester, tetraacetate
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
  • Packaging
  • price
  • TRC
  • 5-Bromo-β-D-glucopyranuronicAcidMethylEsterTetraacetate
  • 1g
  • $ 105.00
Total 3 raw suppliers
Chemical Property of .beta.-D-Glucopyranuronic acid, 5-C-bromo-, methyl ester, tetraacetate
Chemical Property:
  • Melting Point:>130°C (dec.) 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
Purity/Quality:

99% *data from raw suppliers

5-Bromo-β-D-glucopyranuronicAcidMethylEsterTetraacetate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 5-Bromo-β-D-glucopyranuronic Acid Methyl Ester Tetraacetate is an intermediate in the synthesis of heparin building blocks.
Technology Process of .beta.-D-Glucopyranuronic acid, 5-C-bromo-, methyl ester, tetraacetate

There total 2 articles about .beta.-D-Glucopyranuronic acid, 5-C-bromo-, methyl ester, tetraacetate 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:
entspr. Ester 4, N-Bromsuccinimid;
Guidance literature:
With tri-n-butyl-tin hydride; In toluene; for 30h; Product distribution; Heating; variation of scale and reaction time; practical conversion of a D-glucuronic acid derivative into L-iduronic acid derivative by reductive epimerization (after a photobromination);
DOI:10.1016/S0008-6215(00)90357-4
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