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1,3,4,6-tetra-O-acetylhexopyranose

Base Information
  • Chemical Name:1,3,4,6-tetra-O-acetylhexopyranose
  • CAS No.:13036-15-2
  • Molecular Formula:C14H20 O10
  • Molecular Weight:348.307
  • Hs Code.:
1,3,4,6-tetra-O-acetylhexopyranose

Synonyms:Glucopyranose,1,3,4,6-tetraacetate, b-D- (8CI); 1,3,4,6-Tetra-O-acetyl-b-D-glucopyranose; NSC 231870

Suppliers and Price of 1,3,4,6-tetra-O-acetylhexopyranose
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
Total 4 raw suppliers
Chemical Property of 1,3,4,6-tetra-O-acetylhexopyranose
Chemical Property:
  • Vapor Pressure:5.03E-09mmHg at 25°C 
  • Boiling Point:425.5°Cat760mmHg 
  • Flash Point:148.7°C 
  • Density:1.33g/cm3 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1,3,4,6-tetra-O-acetylhexopyranose

There total 4 articles about 1,3,4,6-tetra-O-acetylhexopyranose 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:
Multi-step reaction with 2 steps
1: ammonium cerium (IV) nitrate / acetonitrile / 3 h / 20 °C / Molecular sieve
2: water / acetonitrile / 6 h / 20 °C
With ammonium cerium (IV) nitrate; water; In acetonitrile;
DOI:10.1039/c8ob00477c
Guidance literature:
Multi-step reaction with 2 steps
1: silver nitrate / acetonitrile / 0.08 h / 20 °C / Molecular sieve
2: water / acetonitrile / 6 h / 20 °C
With water; silver nitrate; In acetonitrile;
DOI:10.1039/c8ob00477c
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