175136-66-0

Basic information

• Product Name: 3,3',5,5'-TETRAKIS(TRIFLUOROMETHYL)BENZOPHENONE
• Synonyms: Bis[3,5-bis(trifluoromethyl)phenyl]methanone;DI[3,5-DI(TRIFLUOROMETHYL)PHENYL]METHANONE;3,3',5,5'-TETRAKIS(TRIFLUOROMETHYL)BENZOPHENONE;3,3',5,5'-Tetrakis(trifluoromethyl)benzophenone 97%;3,3',5,5'-Tetrakis(trifluoromethyl)benzophenone97%;3,3',5,5'-Tetra(trifluoromethyl)benzophenone;3,3',5,5'-Tetra(;3,5,3',5'-Tetrakis(trifluoromethyl)benzophenone
• CAS NO: 175136-66-0
• Molecular Formula: C17H6F12O
• Molecular Weight: 454.21
• Mol File: 175136-66-0.mol

Chemical Properties

• Melting Point: 139-140°C
• Boiling Point: 325.2±42.0 °C(Predicted)
• Appearance: /
• Density: 1.506±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• Water Solubility: Sparingly soluble in water.
• CAS DataBase Reference: 3,3',5,5'-TETRAKIS(TRIFLUOROMETHYL)BENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3',5,5'-TETRAKIS(TRIFLUOROMETHYL)BENZOPHENONE(175136-66-0)
• EPA Substance Registry System: 3,3',5,5'-TETRAKIS(TRIFLUOROMETHYL)BENZOPHENONE(175136-66-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 175136-66-0(Hazardous Substances Data)

Usage

Uses

3,3',5,5'-Tetrakis(trifluoromethyl)benzophenone, is used as reactive dye intermediates.

Upstream product

• 87901-76-6 Bis-(3,5-bis-trifluoromethyl-phenyl)-methanol 
• 328-70-1 3,6-bis(trifluoromethyl)bromobenzene 
• 98-86-2 acetophenone 

Downstream Products

• 1055316-03-4 [(Et₃P)2Rh(OC(3,5-(CF₃)2C₆H₃)2(vinyl))] 
• 1055315-89-3 [(Et₃P)3Rh(3,5-(CF₃)2C₆H₃)] 

Relevant articles and documents

Hierarchically Mesoporous o-Hydroxyazobenzene Polymers: Synthesis and Their Applications in CO2Capture and Conversion

The synthesis of hierarchically mesoporous polymers with multiple functionalities is challenging. Herein we reported a template-free strategy for synthesis of phenolic azo-polymers with hierarchical porous structures based on diazo-coupling reaction in aq

One-pot synthesis of diarylmethanones through palladium-catalyzed sequential coupling and aerobic oxidation of aryl bromides with acetophenone as a latent carbonyl donor

A one-pot palladium-catalyzed synthesis of symmetrical and unsymmetrical diarylmethanones using acetophenone and aryl bromides as raw materials has been developed. In this reaction, acetophenone acts as a latent carbonyl donor and two pathways of palladium-catalyzed sequential coupling and aerobic oxidation are identified. The reaction is applicable to a spectrum of substrates and delivers the products in moderate to good yields. This method can be used for the synthesis of ketoprofen, a nonsteroidal anti-inflammatory drug, in a two-step procedure and 45% overall yield.