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tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate

Base Information Edit
  • Chemical Name:tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate
  • CAS No.:1256584-74-3
  • Molecular Formula:
  • Molecular Weight:416.29
  • Hs Code.:
  • Mol file:1256584-74-3.mol
tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate

Synonyms:tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate

Suppliers and Price of tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate
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
  • tert-?Butyl4-?(4-?Ethyl-?3-?iodophenyl)?-?4-?methyl-?3-?oxopentanoate
  • 1mg
  • $ 165.00
Total 5 raw suppliers
Chemical Property of tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate Edit
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

tert-?Butyl4-?(4-?Ethyl-?3-?iodophenyl)?-?4-?methyl-?3-?oxopentanoate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses tert-?Butyl 4-?(4-?Ethyl-?3-?iodophenyl)?-?4-?methyl-?3-?oxopentanoate is an intermediate of Alectinib (C183360), a highly selective and potent anaplastic lymphoma kinase (ALK) inhibitor capable of blocking the resistant gatekeeper mutant, which results in reduced cell growth.
Technology Process of tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate

There total 7 articles about tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoate 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:
mono-tert-butyl malonate; With triethylamine; magnesium chloride; In tetrahydrofuran; at 10 - 30 ℃; for 2h; Inert atmosphere;
2-(4-ethyl-3-iodophenyl)-2-methylpropanoic acid; With 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 10 - 65 ℃; for 7h; Inert atmosphere;
Guidance literature:
With sodium methylate; In methanol; at 50 ℃; for 6h;
Guidance literature:
Multi-step reaction with 5 steps
1.1: aluminum (III) chloride / 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran / -10 °C
2.1: zinc dibromide / 95 °C
3.1: sodium hydroxide; water / methanol / Reflux
4.1: N-iodo-succinimide; methanesulfonic acid / acetonitrile / 15 - 25 °C
5.1: magnesium chloride; triethylamine / tetrahydrofuran / 2 h / 10 - 30 °C / Inert atmosphere
5.2: 7 h / 10 - 65 °C / Inert atmosphere
With aluminum (III) chloride; N-iodo-succinimide; methanesulfonic acid; water; triethylamine; sodium hydroxide; magnesium chloride; zinc dibromide; In tetrahydrofuran; methanol; 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; acetonitrile;
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