Ethyl 2-methylnonanoate

Base Information

Chemical Name:Ethyl 2-methylnonanoate
CAS No.:2458-99-3
Molecular Formula:C12H24O2
Molecular Weight:200.321
Hs Code.:
DSSTox Substance ID:DTXSID101286773

Synonyms:ethyl 2-methylnonanoate;2458-99-3;2-Methylnonanoic acid ethyl ester;SCHEMBL6117662;DTXSID101286773;MFCD11555091;Nonanoic acid, 2-methyl-, ethyl ester;2-Methylnonanoic acid ethyl ester, 97%

Suppliers and Price of Ethyl 2-methylnonanoate

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

Total 5 raw suppliers

Chemical Property of Ethyl 2-methylnonanoate

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:9
Exact Mass:200.177630004
Heavy Atom Count:14
Complexity:143

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC(C)C(=O)OCC

Technology Process of Ethyl 2-methylnonanoate

There total 1 articles about Ethyl 2-methylnonanoate 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:

: 124-11-8
non-1-ene

: 64-17-5
ethanol

: 201230-82-2
carbon monoxide

: 110-38-3
decanoic acid ethyl ester

: 2458-99-3
2-methyl-nonanoic acid ethyl ester

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; tin(ll) chloride; In acetone; for 6h; under 9880 Torr; Product distribution; influence of additions of SnCl₂ on the yield and regioselectivity of the hydrocarboalkoxylation reaction;
DOI:10.1007/BF00955804