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2,5-Thiazoledimethanol

Base Information
  • Chemical Name:2,5-Thiazoledimethanol
  • CAS No.:326850-61-7
  • Molecular Formula:C5H7NO2S
  • Molecular Weight:145.182
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40435938
  • Wikidata:Q82251080
  • Mol file:326850-61-7.mol
2,5-Thiazoledimethanol

Synonyms:2,5-Thiazoledimethanol;326850-61-7;thiazole-2,5-diyldimethanol;SCHEMBL2956791;DTXSID40435938;2,5-di(hydroxymethyl)-1,3-thiazole

Suppliers and Price of 2,5-Thiazoledimethanol
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 2 raw suppliers
Chemical Property of 2,5-Thiazoledimethanol
Chemical Property:
  • PSA:81.59000 
  • LogP:0.12770 
  • XLogP3:-0.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:145.01974964
  • Heavy Atom Count:9
  • Complexity:91
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(SC(=N1)CO)CO
Technology Process of 2,5-Thiazoledimethanol

There total 6 articles about 2,5-Thiazoledimethanol 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 sodium tetrahydroborate; In tetrahydrofuran; methanol; at 5 ℃; for 9h;
DOI:10.1134/S1070363215080113
Guidance literature:
With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 5 ℃; for 9h;
DOI:10.1134/S1070363215080113
Guidance literature:
Multi-step reaction with 3 steps
1: sodium tetrahydroborate
2: water; toluene-4-sulfonic acid / acetonitrile / 9 h / Reflux
3: sodium tetrahydroborate / tetrahydrofuran; methanol / 9 h / 5 °C
With sodium tetrahydroborate; water; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1134/S1070363215080113
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