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ethyl 3-bromo-5-cyanobenzoate

Base Information Edit
  • Chemical Name:ethyl 3-bromo-5-cyanobenzoate
  • CAS No.:1229442-86-7
  • Molecular Formula:C10H8BrNO2
  • Molecular Weight:254.083
  • Hs Code.:
  • Mol file:1229442-86-7.mol
ethyl 3-bromo-5-cyanobenzoate

Synonyms:ethyl 3-bromo-5-cyanobenzoate

Suppliers and Price of ethyl 3-bromo-5-cyanobenzoate
Supply Marketing:Edit
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
  • Crysdot
  • Ethyl3-bromo-5-cyanobenzoate 95+%
  • 1g
  • $ 402.00
  • Alichem
  • Ethyl3-bromo-5-cyanobenzoate
  • 1g
  • $ 1579.40
Total 1 raw suppliers
Chemical Property of ethyl 3-bromo-5-cyanobenzoate Edit
Chemical Property:
Purity/Quality:

98%min *data from raw suppliers

Ethyl3-bromo-5-cyanobenzoate 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of ethyl 3-bromo-5-cyanobenzoate

There total 3 articles about ethyl 3-bromo-5-cyanobenzoate 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:
Guidance literature:
With tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 80 ℃; for 1h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.6b00829
Guidance literature:
Multi-step reaction with 2 steps
1: sulfuric acid / 5 h / 90 °C
2: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 1 h / 80 °C / Inert atmosphere
With tetrakis(triphenylphosphine) palladium(0); sulfuric acid; In N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.6b00829
Refernces Edit
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