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5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide

Base Information
  • Chemical Name:5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide
  • CAS No.:20271-34-5
  • Molecular Formula:C10H11N5S
  • Molecular Weight:233.297
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10405143
  • Nikkaji Number:J3.403.882A
  • NSC Number:111591
5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide

Synonyms:5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide;20271-34-5;5-amino-1-benzyltriazole-4-carbothioamide;NSC111591;5-amino-1-benzyl-triazole-4-carbothioamide;C10H11N5S;DTXSID10405143;NSC 111591;NSC-111591;EN300-297926

Suppliers and Price of 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide
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 6 raw suppliers
Chemical Property of 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide
Chemical Property:
  • Vapor Pressure:2.95E-10mmHg at 25°C 
  • Boiling Point:503.3°Cat760mmHg 
  • Flash Point:258.2°C 
  • Density:1.46g/cm3 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:233.07351655
  • Heavy Atom Count:16
  • Complexity:254
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CN2C(=C(N=N2)C(=S)N)N
Technology Process of 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide

There total 3 articles about 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carbothioamide 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 ethanol; hydrogen sulfide; ammonia;
DOI:10.1021/ja01603a033
Guidance literature:
Multi-step reaction with 2 steps
1: ethanolic sodium ethylate
2: ethanol; NH3; H2S
With ethanol; hydrogen sulfide; ammonia; sodium ethanolate;
DOI:10.1021/ja01603a033

Reference yield:

Guidance literature:
4-Amino-3-benzyl-5-cyano-1,2,3-triazol/H2S in Et3N u.Py.;
DOI:10.1039/P19770000210
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