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Thiazafluron

Base Information Edit
  • Chemical Name:Thiazafluron
  • CAS No.:25366-23-8
  • Molecular Formula:C6H7 F3 N4 O S
  • Molecular Weight:240.209
  • Hs Code.:29349990
  • European Community (EC) Number:246-901-4
  • UNII:WX8ID0K28Q
  • DSSTox Substance ID:DTXSID20180010
  • Nikkaji Number:J3.477K
  • Wikidata:Q22808962
  • Mol file:25366-23-8.mol
Thiazafluron

Synonyms:N,N-dimethyl-N'-(5-trifluromethyl-1,3,4-thiadiazol-2-yl)urea;thiazafluron;thiazaflurone

Suppliers and Price of Thiazafluron
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
  • aablocks
  • THIAZAFLURON
  • 250mg
  • $ 278.00
Total 11 raw suppliers
Chemical Property of Thiazafluron Edit
Chemical Property:
  • Melting Point:136.5°C 
  • Boiling Point:°Cat760mmHg 
  • PKA:13.14±0.46(Predicted) 
  • Flash Point:°C 
  • PSA:86.36000 
  • Density:1.507g/cm3 
  • LogP:1.72340 
  • Water Solubility.:2.096g/L(20 oC) 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:1
  • Exact Mass:240.02926652
  • Heavy Atom Count:15
  • Complexity:249
Purity/Quality:

98% *data from raw suppliers

THIAZAFLURON *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn,N 
  • Statements: 22-50/53 
  • Safety Statements: 60-61 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CNC(=O)N(C)C1=NN=C(S1)C(F)(F)F
Technology Process of Thiazafluron

There total 3 articles about Thiazafluron 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 triethylamine; In toluene; at 30 - 75 ℃; for 5h; Temperature; Reagent/catalyst;
Guidance literature:
2-Dimethylamino-5-trifluormethyl-1,3,4-thiadiazol, HNCO;
Refernces Edit
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