2,3,4-Trifluorobenzophenone

Base Information

Chemical Name:2,3,4-Trifluorobenzophenone
CAS No.:243448-18-2
Molecular Formula:C₁₃H₇F₃O
Molecular Weight:236.193
Hs Code.:
DSSTox Substance ID:DTXSID201282324
Nikkaji Number:J3.378.711A

Synonyms:2,3,4-Trifluorobenzophenone;243448-18-2;Methanone, phenyl(2,3,4-trifluorophenyl)-;Phenyl-(2,3,4-trifluorophenyl)methanone;phenyl(2,3,4-trifluorophenyl)methanone;o,m,p-Trifluorobenzophenone;SCHEMBL5613025;DTXSID201282324;MFCD00083550;AKOS009158093;Phenyl-(2,3,4-trifluoro-phenyl)-methanone

Suppliers and Price of 2,3,4-Trifluorobenzophenone

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2,3,4-Trifluorobenzophenone

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:236.04489933
Heavy Atom Count:17
Complexity:276

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C2=C(C(=C(C=C2)F)F)F

Technology Process of 2,3,4-Trifluorobenzophenone

There total 2 articles about 2,3,4-Trifluorobenzophenone 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: 55.0%

: 1620086-18-1
1,2,3-trifluoro-4-(1-phenylvinyl)benzene

: 243448-18-2
phenyl(2,3,4-trifluorophenyl)methanone

Guidance literature:: With 2,2'-azobis(isobutyronitrile); oxygen; In nitromethane; at 60 ℃; for 12h; Schlenk technique;
DOI:10.1021/jo501203a

Reference yield:

: 536-74-3
phenylacetylene

: 226396-32-3
(2,3,4-trifluorophenyl)boronic acid

: 243448-18-2
phenyl(2,3,4-trifluorophenyl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; acetic acid / 1,4-dioxane / 12 h / 80 °C / Schlenk technique; Inert atmosphere

2: 2,2'-azobis(isobutyronitrile); oxygen / nitromethane / 12 h / 60 °C / Schlenk technique

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; 2,2'-azobis(isobutyronitrile); oxygen; acetic acid; In 1,4-dioxane; nitromethane;
DOI:10.1021/jo501203a