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Technology Process of 2-chloro-N-(5-methylsulfanyl-1,2,4-thiadiazol-3-yl)acetamide

2-chloro-N-(5-methylsulfanyl-1,2,4-thiadiazol-3-yl)acetamide

Base Information
  • Chemical Name:2-chloro-N-(5-methylsulfanyl-1,2,4-thiadiazol-3-yl)acetamide
  • CAS No.:78429-98-8
  • Molecular Formula:C5H6 Cl N3 O S2
  • Molecular Weight:223.7
  • Hs Code.:2934999090
  • DSSTox Substance ID:DTXSID70375691
  • Wikidata:Q82164316
  • Mol file:78429-98-8.mol
2-chloro-N-(5-methylsulfanyl-1,2,4-thiadiazol-3-yl)acetamide

Synonyms:78429-98-8;2-chloro-N-(5-methylsulfanyl-1,2,4-thiadiazol-3-yl)acetamide;2-Chloro-N-[5-(methylsulfanyl)-1,2,4-thiadiazol-3-yl]acetamide;2-chloro-N-(5-(methylthio)-1,2,4-thiadiazol-3-yl)acetamide;2-CHLORO-N-(5-METHYLTHIO-1,2,4-THIADIAZOL-3-YL)ACETAMIDE;DTXSID70375691;Acetamide,2-chloro-N-[5-(methylthio)-1,2,4-thiadiazol-3-yl]-;MFCD06658063;3-(2-Chloroacetamido)-5-(methylthio)-1,2,4-thiadiazole

Suppliers and Price of 2-chloro-N-(5-methylsulfanyl-1,2,4-thiadiazol-3-yl)acetamide
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
  • 2-CHLORO-N-(5-METHYLTHIO-1,2,4-THIADIAZOL-3-YL)ACETAMIDE 95.00%
  • 5MG
  • $ 504.81
Total 4 raw suppliers
Chemical Property of 2-chloro-N-(5-methylsulfanyl-1,2,4-thiadiazol-3-yl)acetamide
Chemical Property:
  • Refractive Index:1.619 
  • PKA:9.67±0.70(Predicted) 
  • PSA：108.42000 
  • Density:1.53g/cm3 
  • LogP:1.51030 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:3
  • Exact Mass:222.9640819
  • Heavy Atom Count:12
  • Complexity:171
Purity/Quality:

98%Min *data from raw suppliers

2-CHLORO-N-(5-METHYLTHIO-1,2,4-THIADIAZOL-3-YL)ACETAMIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CSC1=NC(=NS1)NC(=O)CCl
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