2-Ethyl-2-methylvaleric acid methyl ester

Base Information

Chemical Name:2-Ethyl-2-methylvaleric acid methyl ester
CAS No.:37974-23-5
Molecular Formula:C9H18O2
Molecular Weight:158.241
Hs Code.:2915900090
Mol file:37974-23-5.mol

Synonyms:2-Ethyl-2-methylpentansaeuremethylester;Pentanoic acid,2-ethyl-2-methyl-,methyl ester;2-ethyl-2-methyl-valeric acid methyl ester;2-Aethyl-2-methyl-valeriansaeure-methylester;

Suppliers and Price of 2-Ethyl-2-methylvaleric acid methyl ester

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
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price

Total 1 raw suppliers

Chemical Property of 2-Ethyl-2-methylvaleric acid methyl ester

Chemical Property:

PSA：26.30000
LogP:2.37580

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-Ethyl-2-methylvaleric acid methyl ester

There total 5 articles about 2-Ethyl-2-methylvaleric acid methyl ester 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:

Reference yield:

: 868-57-5
methyl 2-methylbutanoate

: 107-08-4
1-iodo-propane

: 37974-23-5
2-ethyl-2-methyl-valeric acid methyl ester

Guidance literature:: methyl 2-methylbutanoate; With lithium diisopropyl amide; at -78 ℃; for 1h;

1-iodo-propane; at -78 - 20 ℃;
DOI:10.1021/ja413131m

Reference yield:

: 15726-15-5
3-methyl-4-heptanone

: 37974-23-5
2-ethyl-2-methyl-valeric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: bromine

2: diethyl ether

With diethyl ether; bromine;
DOI:10.1021/ja01254a024