α-[4-(Trifluoromethyl)phenyl]benzhydryl alcohol

Base Information

Chemical Name:α-[4-(Trifluoromethyl)phenyl]benzhydryl alcohol
CAS No.:21856-96-2
Molecular Formula:C20H15F3O
Molecular Weight:328.334
Hs Code.:
Mol file:21856-96-2.mol

Synonyms:4-(Trifluoromethyl)trityl alcohol;Diphenyl(α,α,α-trifluoro-p-tolyl)methanol;α-[4-(Trifluoromethyl)phenyl]benzhydryl alcohol

Suppliers and Price of α-[4-(Trifluoromethyl)phenyl]benzhydryl alcohol

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 α-[4-(Trifluoromethyl)phenyl]benzhydryl alcohol

Chemical Property:

PSA：20.23000
LogP:4.98960

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of α-[4-(Trifluoromethyl)phenyl]benzhydryl alcohol

There total 9 articles about α-[4-(Trifluoromethyl)phenyl]benzhydryl alcohol 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: 73.0%

: 119-61-9
benzophenone

: 402-43-7
p-trifluoromethylphenyl bromide

: 21856-96-2
Diphenyl<4-(trifluormethyl)phenyl>methanol

Guidance literature:: p-trifluoromethylphenyl bromide; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 2h;

benzophenone; In tetrahydrofuran; hexane; at 20 ℃; for 4h;

Reference yield:

: 76-84-6
triphenylmethyl alcohol

: 21856-96-2
Diphenyl<4-(trifluormethyl)phenyl>methanol

Guidance literature:: Multi-step reaction with 2 steps

1: Cs₂CO₃; Pd(OAc)2; PCy₃ / o-xylene / Heating

With palladium diacetate; caesium carbonate; tricyclohexylphosphine; In o-xylene;
DOI:10.1021/jo0344034