1-(3-Fluorophenyl)cyclohexanecarbonitrile

Base Information Edit

Chemical Name:1-(3-Fluorophenyl)cyclohexanecarbonitrile
CAS No.:214262-91-6
Molecular Formula:C13H14FN
Molecular Weight:203.259
Hs Code.:
DSSTox Substance ID:DTXSID20352932
Wikidata:Q82130364
Mol file:214262-91-6.mol

Synonyms:1-(3-FLUOROPHENYL)CYCLOHEXANECARBONITRILE;214262-91-6;1-(3-fluorophenyl)cyclohexane-1-carbonitrile;6-(3-FLUOROPHENYL)CYCLOHEXANECARBONITRILE;Cyclohexanecarbonitrile,1-(3-fluorophenyl)-;SCHEMBL1020648;DTXSID20352932;AKOS009265988;AB90643;FT-0704409

Suppliers and Price of 1-(3-Fluorophenyl)cyclohexanecarbonitrile

Supply Marketing:Edit

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

American Custom Chemicals Corporation
1-(3-FLUOROPHENYL)CYCLOHEXANE-1-CARBONITRILE 95.00%
5MG
$ 501.73

Acrotein
1-(3-Fluorophenyl)cyclohexanecarbonitrile 97%
1g
$ 91.66

ACHEMBLOCK
1-(3-Fluorophenyl)cyclohexanecarbonitrile 95%
25G
$ 975.00

ACHEMBLOCK
1-(3-Fluorophenyl)cyclohexanecarbonitrile 95%
1G
$ 125.00

Total 9 raw suppliers

Chemical Property of 1-(3-Fluorophenyl)cyclohexanecarbonitrile Edit

Chemical Property:

Vapor Pressure:0.000182mmHg at 25°C
Refractive Index:1.529
Boiling Point:329 °C at 760 mmHg
Flash Point:142.2 °C
PSA：23.79000
Density:1.09 g/cm³
LogP:3.55118
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:203.111027613
Heavy Atom Count:15
Complexity:259

Purity/Quality:

98%Min ^*data from raw suppliers

1-(3-FLUOROPHENYL)CYCLOHEXANE-1-CARBONITRILE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)(C#N)C2=CC(=CC=C2)F

Technology Process of 1-(3-Fluorophenyl)cyclohexanecarbonitrile

There total 2 articles about 1-(3-Fluorophenyl)cyclohexanecarbonitrile 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: 97.0%