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Terrazole mixt. with Thiophanate-methyl

Base Information
  • Chemical Name:Terrazole mixt. with Thiophanate-methyl
  • CAS No.:64491-74-3
  • Molecular Formula:C12H14N4O4S2•C5H5Cl3N2OS
  • Molecular Weight:589.95
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00897356
  • Mol file:64491-74-3.mol
Terrazole mixt. with Thiophanate-methyl

Synonyms:Terrazole mixt. with Thiophanate-methyl;64491-74-3;Thiophanate-methyl mixt. with terrazole;Carbamic acid, (1,2-phenylenebis(iminocarbonothioyl))bis-, dimethyl ester, mixt. with 5-ethoxy-3-(trichloromethyl)-1,2,4-thiadiazole;Carbamic acid, [1,2-phenylenebis(iminocarbonothioyl)]bis-, dimethyl ester, mixt. with 5-ethoxy-3-(trichloromethyl)-1,2,4-thiadiazole;DTXSID00897356;C12H14N4O4S2.C5H5Cl3N2OS;LS-50543;C12-H14-N4-O4-S2.C5-H5-Cl3-N2-O-S

Suppliers and Price of Terrazole mixt. with Thiophanate-methyl
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
  • American Custom Chemicals Corporation
  • (1,2-PHENYLENEBIS(IMINOCARBONOTHIO-YL))BISCARBAMIC ACID DIMETHYL ESTER MIXED WITH 5-ETHOXY-3-(TRICHLOROMETHYL)-1,2,4-THIADIAZOLE 95.00%
  • 5MG
  • $ 498.71
Total 3 raw suppliers
Chemical Property of Terrazole mixt. with Thiophanate-methyl
Chemical Property:
  • Vapor Pressure:9.18E-15mmHg at 25°C 
  • Boiling Point:608.8°C at 760 mmHg 
  • Flash Point:322°C 
  • PSA:249.21000 
  • LogP:5.40550 
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:6
  • Exact Mass:587.964464
  • Heavy Atom Count:34
  • Complexity:561
Purity/Quality:

99% *data from raw suppliers

(1,2-PHENYLENEBIS(IMINOCARBONOTHIO-YL))BISCARBAMIC ACID DIMETHYL ESTER MIXED WITH 5-ETHOXY-3-(TRICHLOROMETHYL)-1,2,4-THIADIAZOLE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC1=NC(=NS1)C(Cl)(Cl)Cl.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC
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