733-83-5

Basic information

• Product Name: BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL
• Synonyms: 1,1-BIS(4(FLUOROPHENYL)TRIFLUOROETHANOL);BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL;2,2,2-trifluoro-1,1-bis(4-fluorophenyl)ethanol;Bis(4-fluorophenyl)trifluoromethylcarbinol97%
• CAS NO: 733-83-5
• Molecular Formula: C₁₄H₉F₅O
• Molecular Weight: 288.21
• Mol File: 733-83-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 111-114°C 3mm
• Flash Point: >110°C
• Appearance: /
• Density: 1.382 g/cm³
• Vapor Pressure: 9.97E-05mmHg at 25°C
• Refractive Index: 1.504
• CAS DataBase Reference: BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL(733-83-5)
• EPA Substance Registry System: BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL(733-83-5)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 733-83-5(Hazardous Substances Data)

Usage

General Description

BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL is a chemical compound that is formed by two 4-fluorophenyl groups attached to a trifluoromethyl carbinol group. It is a colorless liquid that is used in various chemical reactions and synthesis processes. The compound has potential applications in pharmaceutical and agrochemical industries due to its unique chemical properties. BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL is also known for its role as a reagent in organic chemistry, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. The compound is considered to be a valuable building block for the synthesis of various organic molecules, making it an important component in the field of chemical research and development.

InChI:InChI=1/C14H9F5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H

Upstream product

• 383-63-1 ethyl trifluoroacetate, 
• 352-13-6 4-flourophenylmagnesium bromide 
• 407-25-0 trifluoroacetic anhydride 
• 75-46-7 trifluoromethan 
• 1586-73-8 tris(trimethylsilyl)amine 
• 345-92-6 4,4'-Difluorobenzophenone 
• 345959-36-6 1-(4-benzylpiperazin-1-yl)-2, 2, 2-trifluoroethanol 

Downstream Products

• 789-03-7 1,1,1-trifluoro-2,2-bis(p-fluorophenyl)ethane 
• 2247-78-1 N-<1,1-Bis-(4-fluor-phenyl)-2,2,2-trifluor-aethyl>-acetamid 
• 192826-37-2 toluene-4-sulfonic acid 2,2,2-trifluoro-1,1-bis-(4-fluoro-phenyl)-ethyl ester 
• 361-63-7 2,2-bis(4-fluorophenyl)acetic acid 
• 386-99-2 ethyl 2,2-bis(4-fluorophenyl)acetate 

Relevant articles and documents

Trifluoromethylation of nonenolizable carbonyl compounds with a stable piperazino hemiaminal of trifluoroacetaldehyde

A new stable hemiaminal of fluoral (1) can easily be obtained from the methyl hemiketal of fluoral and N-benzylpiperazine. This white crystalline compound can be used under basic conditions as an efficient nucleophilic trifluoromethylating reagent towards nonenolizable carbonyl compounds.

Substituent Effects on the Solvolysis of 1,1-Diphenyl-2,2,2-trifluoroethyl Tosylates: Comparison between Symmetrically Disubstituted and Monosubstituted Systems

The solvolysis rates of 1-(substituted phenyl)-1-phenyl-2,2,2-trifluoroethyl and 1,1-bis(substituted phenyl)-2,2,2-trifluoroethyl tosylates or bromides were conductimetrically measured at 25.0 °C in 80% aqueous ethanol. The substituent effects on these so