Cyclooctyl 2-methylpropanoate

Base Information

Chemical Name:Cyclooctyl 2-methylpropanoate
CAS No.:91165-04-7
Molecular Formula:C12H22O2
Molecular Weight:198.305
Hs Code.:
DSSTox Substance ID:DTXSID90530462
Wikidata:Q82401602

Synonyms:Cyclooctyl 2-methylpropanoate;91165-04-7;SCHEMBL26822901;DTXSID90530462

Suppliers and Price of Cyclooctyl 2-methylpropanoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Cyclooctyl 2-methylpropanoate

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:198.161979940
Heavy Atom Count:14
Complexity:167

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)C(=O)OC1CCCCCCC1

Technology Process of Cyclooctyl 2-methylpropanoate

There total 5 articles about Cyclooctyl 2-methylpropanoate 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: 62.0%

: 696-71-9
cyclooctanol

: 79-30-1
isobutyryl chloride

: 91165-04-7
cyclo-octyl isobutyrate

Guidance literature:: cyclooctanol; With triethylamine; In dichloromethane; at 0 ℃; for 0.0833333h;

isobutyryl chloride; In dichloromethane; at 0 - 20 ℃; for 3h;
DOI:10.1039/c9cc02060h

Reference yield:

: 772-60-1
cyclooctyl acetate

: 91165-04-7
cyclo-octyl isobutyrate

Guidance literature:: Multi-step reaction with 2 steps

1: 1) bromomagnesium diisopropylamide; 2) methyl iodide, 15 percent HCl / 1) -40 deg C, ether, 2 h; 2) benzene, reflux, 2 h; RT, 15 min

2: DMAP / pyridine

With hydrogenchloride; dmap; bromomagnesium diisopropylamide; methyl iodide; In pyridine;
DOI:10.1016/S0040-4020(01)88162-X

Reference yield:

: 42463-67-2
Cyclooctyl-phenylacetat

: 91165-04-7
cyclo-octyl isobutyrate

Guidance literature:: Multi-step reaction with 2 steps

1: 1) LDA; 2) methyl iodide, 15 percent HCl / 1) THF, -78 deg C; 2) THF, reflux 2 h; RT, 15 min

2: DMAP / pyridine

With hydrogenchloride; dmap; lithium diisopropyl amide; methyl iodide; In pyridine;
DOI:10.1016/S0040-4020(01)88162-X