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Technology Process of N7-(3-Chlorophenyl)-N2-phenylthiazolo[5,4-d]pyrimidine-2,7-diamine

N7-(3-Chlorophenyl)-N2-phenylthiazolo[5,4-d]pyrimidine-2,7-diamine

Base Information
  • Chemical Name:N7-(3-Chlorophenyl)-N2-phenylthiazolo[5,4-d]pyrimidine-2,7-diamine
  • CAS No.:871266-94-3
  • Molecular Formula:C17H12 Cl N5 S
  • Molecular Weight:353.83
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30467667
  • Wikidata:Q82294711
  • Mol file:871266-94-3.mol
N7-(3-Chlorophenyl)-N2-phenylthiazolo[5,4-d]pyrimidine-2,7-diamine

Synonyms:871266-94-3;N7-(3-Chlorophenyl)-N2-phenylthiazolo[5,4-d]pyrimidine-2,7-diamine;7-N-(3-chlorophenyl)-2-N-phenyl-[1,3]thiazolo[5,4-d]pyrimidine-2,7-diamine;DTXSID30467667;N~7~-(3-Chlorophenyl)-N~2~-phenyl[1,3]thiazolo[5,4-d]pyrimidine-2,7-diamine

Suppliers and Price of N7-(3-Chlorophenyl)-N2-phenylthiazolo[5,4-d]pyrimidine-2,7-diamine
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
  • N-7-(3-CHLOROPHENYL)-N-2-PHENYLTHIAZOLO-[5,4-D]PYRIMIDINE-2,7-DIAMINE 95.00%
  • 5MG
  • $ 500.96
Total 5 raw suppliers
Chemical Property of N7-(3-Chlorophenyl)-N2-phenylthiazolo[5,4-d]pyrimidine-2,7-diamine
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.791 
  • Boiling Point:551.757°C at 760 mmHg 
  • Flash Point:287.492°C 
  • PSA：90.97000 
  • Density:1.495g/cm3 
  • LogP:5.37290 
  • XLogP3:5.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:4
  • Exact Mass:353.0501943
  • Heavy Atom Count:24
  • Complexity:408
Purity/Quality:

97% *data from raw suppliers

N-7-(3-CHLOROPHENYL)-N-2-PHENYLTHIAZOLO-[5,4-D]PYRIMIDINE-2,7-DIAMINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)NC2=NC3=C(N=CN=C3S2)NC4=CC(=CC=C4)Cl
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