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Cyclooctyl 2-methylpropanoate

Base Information Edit
  • 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
  • Mol file:91165-04-7.mol
Cyclooctyl 2-methylpropanoate

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

Suppliers and Price of Cyclooctyl 2-methylpropanoate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of Cyclooctyl 2-methylpropanoate Edit
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:
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
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
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
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