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D-tagaturonic acid

Base Information Edit
  • Chemical Name:D-tagaturonic acid
  • CAS No.:6812-01-7
  • Molecular Formula:C6H10O7
  • Molecular Weight:194.141
  • Hs Code.:
  • DSSTox Substance ID:DTXSID001344855
  • Nikkaji Number:J1.367.593G
  • Wikidata:Q27109371
  • Metabolomics Workbench ID:53822
  • Mol file:6812-01-7.mol
D-tagaturonic acid

Synonyms:D-tagaturonic acid;D-arabino-hex-5-ulosonic acid;(2S,3R,4S)-2,3,4,6-tetrahydroxy-5-oxohexanoic acid;6812-01-7;SCHEMBL5802682;CHEBI:21099;DTXSID001344855;LMFA05000654;Q27109371

Suppliers and Price of D-tagaturonic acid
Supply Marketing:Edit
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 0 raw suppliers
Chemical Property of D-tagaturonic acid Edit
Chemical Property:
  • XLogP3:-3
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:5
  • Exact Mass:194.04265265
  • Heavy Atom Count:13
  • Complexity:201
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(=O)C(C(C(C(=O)O)O)O)O)O
  • Isomeric SMILES:C(C(=O)[C@H]([C@H]([C@@H](C(=O)O)O)O)O)O
Technology Process of D-tagaturonic acid

There total 2 articles about D-tagaturonic 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:
With water; bromine; Unter Ausschluss von Licht; Erwaermen der von Brom und Bromid befreiten Reaktionsloesung mit Bariumcarbonat.;
DOI:10.1021/ja01876a052
Guidance literature:
at 25 ℃; Equilibrium constant; Katalysierte Isomerisierung; pH 7.;
upstream raw materials:

L-galactonic acid

L-Rhamnose

Downstream raw materials:

D-galacturonic acid

Refernces Edit
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