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5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, monohydrochloride

Base Information
  • Chemical Name:5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, monohydrochloride
  • CAS No.:71205-32-8
  • Molecular Formula:C7H8ClN5S
  • Molecular Weight:229.6899
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20887774
  • Mol file:71205-32-8.mol
5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, monohydrochloride

Synonyms:71205-32-8;5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, monohydrochloride;1-(3-Aminophenyl)-1H-tetrazole-5-thiol hydrochloride;5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, hydrochloride (1:1);1-(3-aminophenyl)-2H-tetrazole-5-thione;hydrochloride;5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, hydrochloride;14124-34-6;1-(3-aminophenyl)-2H-tetrazole-5-thione hydrochloride;C7H7N5S.ClH;C7-H7-N5-S.Cl-H;SCHEMBL8020291;DTXSID20887774;BMRLZHWIMPOGRN-UHFFFAOYSA-N;1-(3-aminophenyl)-5-mercaptotetrazole hydrochloride;1-(3-aminophenyl)- 5-mercaptotetrazole hydrochloride;1-(3-aminophenyl)-5-mercaptotetrazole hydrochloric acid salt;5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,4-dihydro-, monohydrochloride

Suppliers and Price of 5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, monohydrochloride
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
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Total 4 raw suppliers
Chemical Property of 5H-Tetrazole-5-thione, 1-(3-aminophenyl)-1,2-dihydro-, monohydrochloride
Chemical Property:
  • Vapor Pressure:8.72E-05mmHg at 25°C 
  • Boiling Point:340.2°C at 760 mmHg 
  • Flash Point:159.6°C 
  • PSA:104.61000 
  • LogP:2.29030 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:229.0188941
  • Heavy Atom Count:14
  • Complexity:241
Purity/Quality:

98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC(=C1)N2C(=S)N=NN2)N.Cl
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