Fluoromethyl Cyclohexanecarboxylate

Base Information

Chemical Name:Fluoromethyl Cyclohexanecarboxylate
CAS No.:166331-85-7
Molecular Formula:C₈H₁₃FO₂
Molecular Weight:160.188
Hs Code.:
DSSTox Substance ID:DTXSID40453354
Mol file:166331-85-7.mol

Synonyms:Fluoromethyl Cyclohexanecarboxylate;166331-85-7;Cyclohexanecarboxylic acid, fluoromethyl ester (9CI);SCHEMBL13080625;DTXSID40453354

Suppliers and Price of Fluoromethyl Cyclohexanecarboxylate

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 2 raw suppliers

Chemical Property of Fluoromethyl Cyclohexanecarboxylate

Chemical Property:

Boiling Point:202.2±15.0 °C(Predicted)
PSA：26.30000
Density:1.071±0.06 g/cm3(Predicted)
LogP:2.03690
XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:160.08995782
Heavy Atom Count:11
Complexity:130

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)C(=O)OCF

Technology Process of Fluoromethyl Cyclohexanecarboxylate

There total 1 articles about Fluoromethyl Cyclohexanecarboxylate 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: 50.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 1977-87-3
cyclohexanecarbonyl fluoride

: 166331-85-7
fluoromethyl cyclohexanecarboxylate

: (cyclohexanecarbonyloxy)methyl cyclohexanecarboxylate

Guidance literature:: With potassium fluoride; 18-crown-6 ether; In tetrahydrofuran; for 4h; Product distribution; reactions of acylfluorides with CH₂O under var. conditions;
DOI:10.1016/0040-4020(95)00251-3