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7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE

Base Information
  • Chemical Name:7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE
  • CAS No.:160290-42-6
  • Molecular Formula:C11H7ClN4
  • Molecular Weight:0.00000
  • Hs Code.:
  • Mol file:160290-42-6.mol
7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE

Synonyms:

Suppliers and Price of 7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE
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
  • 7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 95.00%
  • 1MG
  • $ 647.61
Total 2 raw suppliers
Chemical Property of 7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE
Chemical Property:
  • Melting Point:226-228 °C(Solv: ethanol (64-17-5)) 
  • PKA:0.15±0.30(Predicted) 
  • PSA:0.00000 
  • Density:1.45±0.1 g/cm3(Predicted) 
  • LogP:0.00000 
Purity/Quality:

99% *data from raw suppliers

7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE

There total 7 articles about 7-(4-CHLOROPHENYL)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 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 sodium hydride; In N,N-dimethyl-formamide; for 12h; Ambient temperature;
DOI:10.1016/S0040-4020(01)89564-8
Guidance literature:
With potassium phosphate; copper(l) iodide; 1,10-Phenanthroline; Trimethylacetic acid; In 1,4-dioxane; at 140 ℃; for 24h; regioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1021/jacs.6b03890
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