1-Trifluoromethyl-1,2-diphenylethylene

Base Information

Chemical Name:1-Trifluoromethyl-1,2-diphenylethylene
CAS No.:76280-44-9
Molecular Formula:C₁₅H₁₁F₃
Molecular Weight:248.248
Hs Code.:
Nikkaji Number:J587.249I,J1.965.127D
Mol file:76280-44-9.mol

Synonyms:1,1-TFMDE;1-trifluoromethyl-1,2-diphenylethylene

Suppliers and Price of 1-Trifluoromethyl-1,2-diphenylethylene

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
Packaging
price

Total 3 raw suppliers

Chemical Property of 1-Trifluoromethyl-1,2-diphenylethylene

Chemical Property:

Boiling Point:293.8oC at 760 mmHg
Flash Point:113.8oC
PSA：0.00000
Density:1.188g/cm3
LogP:4.78950
XLogP3:5.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:248.08128484
Heavy Atom Count:18
Complexity:279

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=C(C2=CC=CC=C2)C(F)(F)F
Isomeric SMILES:C1=CC=C(C=C1)/C=C(\C2=CC=CC=C2)/C(F)(F)F

Technology Process of 1-Trifluoromethyl-1,2-diphenylethylene

There total 37 articles about 1-Trifluoromethyl-1,2-diphenylethylene 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: 93.0%

: 13652-07-8
phenyltrifluorodiazoethane

: 100-39-0
benzyl bromide

: 76280-44-9,76280-42-7,77542-08-6
(E)-(3,3,3-trifluoroprop-1-ene-1,2-diyl)dibenzene

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trifuran-2-yl-phosphane; triethylamine; lithium tert-butoxide; In toluene; at 80 ℃; for 5h; Reagent/catalyst; Solvent; Temperature; stereoselective reaction; Inert atmosphere; Sealed tube;
DOI:10.1002/chem.201304143