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methyl 4-(2-iodoethyl)benzoate

Base Information Edit
  • Chemical Name:methyl 4-(2-iodoethyl)benzoate
  • CAS No.:1065269-88-6
  • Molecular Formula:C10H11IO2
  • Molecular Weight:290.101
  • Hs Code.:
  • Mol file:1065269-88-6.mol
methyl 4-(2-iodoethyl)benzoate

Synonyms:methyl 4-(2-iodoethyl)benzoate

Suppliers and Price of methyl 4-(2-iodoethyl)benzoate
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
  • TRC
  • Methyl4-(2-Iodoethyl)benzoate
  • 2.5g
  • $ 1320.00
  • Medical Isotopes, Inc.
  • Methyl4-(2-Iodoethyl)benzoate
  • 2.5 g
  • $ 2200.00
  • Medical Isotopes, Inc.
  • Methyl4-(2-Iodoethyl)benzoate
  • 250 mg
  • $ 650.00
  • A1 Biochem Labs
  • Methyl4-(2-iodoethyl)benzoate 95%
  • 5 g
  • $ 1300.00
Total 2 raw suppliers
Chemical Property of methyl 4-(2-iodoethyl)benzoate Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Methyl4-(2-Iodoethyl)benzoate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Methyl 4-(2-Iodoethyl)benzoate is is a 2-pyridone derivative as EP4 receptor agonist for the treatment of peripheral arterial disease. Methyl 4-(2-Iodoethyl)benzoate is a 2-pyridone derivative as EP4 receptor agonist for the treatment of peripheral arterial disease.
Technology Process of methyl 4-(2-iodoethyl)benzoate

There total 2 articles about methyl 4-(2-iodoethyl)benzoate 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 potassium iodide; In acetonitrile; for 72h; Reflux;
Guidance literature:
With 1H-imidazole; iodine; triphenylphosphine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1021/ja100185p
Guidance literature:
With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃;
Refernces Edit
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