(2-Fluoro-1-phenylethenyl)benzene

Base Information Edit

Chemical Name:(2-Fluoro-1-phenylethenyl)benzene
CAS No.:390-75-0
Molecular Formula:C14H11F
Molecular Weight:198.24
Hs Code.:
DSSTox Substance ID:DTXSID40443053
Nikkaji Number:J469.797I
Mol file:390-75-0.mol

Synonyms:390-75-0;1,1-Diphenyl-2-fluoroethene;1,1-Diphenyl-2-fluoro-ethene;1,1-diphenyl-2-fluoroethylene;SCHEMBL10419768;DTXSID40443053;(2-fluoro-1-phenylethenyl)benzene;1,1'-(2-Fluoroethene-1,1-diyl)dibenzene

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

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Chemical Property of (2-Fluoro-1-phenylethenyl)benzene Edit

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:198.084478513
Heavy Atom Count:15
Complexity:187

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=CF)C2=CC=CC=C2

Technology Process of (2-Fluoro-1-phenylethenyl)benzene

There total 45 articles about (2-Fluoro-1-phenylethenyl)benzene 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: 95.0%

: 2-fluoro-3-hydroxy-3,3-diphenylpropionic acid

: 390-75-0
2-fluoro-1,1-diphenylethene

Guidance literature:: 2-fluoro-3-hydroxy-3,3-diphenylpropionic acid; With dmap; p-toluenesulfonyl chloride; In chloroform; at -50 - 0 ℃; for 2h;

In chloroform; at 65 ℃; for 15h;
DOI:10.1135/cccc20021325

Reference yield: 92.0%

: 1262431-36-6
(Z)-2-fluoro-1-phenylvinyl 4-methylbenzenesulfonate

: 98-80-6
phenylboronic acid

: 390-75-0
2-fluoro-1,1-diphenylethene

Guidance literature:: With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; potassium phosphate; tricyclohexylphosphine; In 1,4-dioxane; at 100 ℃; for 14h; stereoselective reaction; Inert atmosphere;
DOI:10.1021/ol102645g