384-94-1

Usage

Chemical structure

Dibenzene derivative with a trifluoroethane bridge

Explanation

The compound consists of two benzene rings connected by a trifluoroethane (CF3-CH2-CH2-CF3) bridge, which is a part of the 1,1-ethanediyl group.

Explanation

The compound appears as a colorless solid with a crystalline structure.

Explanation

The compound does not dissolve in water but can dissolve in organic solvents like alcohols, ethers, and hydrocarbons.

Explanation

Due to its chemical properties and structure, 1,1'-(2,2,2-trifluoro-1,1-ethanediyl)dibenzene is used as a starting material or intermediate in the synthesis of various polymers, pharmaceuticals, and agrochemicals.

Explanation

The compound serves as a versatile building block in the synthesis of other organic compounds, making it valuable in the field of organic chemistry.

Explanation

The compound's properties and structure make it useful in various industrial processes and research applications, such as the development of new materials and the study of chemical reactions.

Physical state

Colorless, crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Applications

Production of polymers, pharmaceuticals, and agrochemicals

Synthesis

Building block for other organic compounds

Industrial and research applications

Wide range of uses

Upstream product

• 119-61-9 benzophenone 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 5350-57-2 benzophenone hydrazone 
• 908093-98-1 diazodiphenylmethane 
• 431-46-9 2,2,2-trifluoro-1-methoxy-ethanol 
• 71-43-2 benzene 
• 434-45-7 2,2,2-Trifluoroacetophenone 
• 340-04-5 1-phenyl-2,2,2-trifluoromethylethanol 
• 433-27-2 ethyl trifluoroacetaldehyde hemiacetal 
• 379-18-0 1,1-diphenyl-2,2,2-trifluoroethanol 

Downstream Products

• 1033-26-7 4,4'-dinitrobenzophenone 
• 102139-48-0 1-fluoro-2,2-bis-(4-nitrophenyl)-1-(pyrrolidin-1-yl)ethene 
• 102139-49-1 1-fluoro-2,2-bis-(4-nitrophenyl)-1-piperidinoethene 
• 102139-50-4 2,2-bis-(4-nitrophenyl)-1,1-bis-(propylamino)ethene 
• 102139-51-5 2,2-bis-(4-nitrophenyl)-1,1-bis-(butylamino)ethene 
• 72837-38-8 1-(1-fluoro-2,2-diphenylvinyl)-1H-imidazole 
• 83004-37-9 4,4'-(2,2-difluoroethenylidene)bis(nitrobenzene) 
• 118446-37-0 1-fluoro-1-phenoxy-2,2-di(4-nitrophenyl)ethene 
• 64416-13-3 1,1,1-trifluoro-2,2-bis-(4-nitrophenyl) ethane 
• 3468-99-3 ethyl diphenylacetate 
• 3469-00-9 methyl 2,2-diphenylacetate 

Relevant academic research and scientific papers

Chemoselective Homologation-Deoxygenation Strategy Enabling the Direct Conversion of Carbonyls into (n+1)-Halomethyl-Alkanes

The sequential installation of a carbenoid and a hydride into a carbonyl, furnishing halomethyl alkyl derivatives, is reported. Despite the employment of carbenoids as nucleophiles in reactions with carbon-centered electrophiles, sp3-type alkyl halides remain elusive materials for selective one-carbon homologations. Our tactic levers on using carbonyls as starting materials and enables uniformly high yields and chemocontrol. The tactic is flexible and is not limited to carbenoids. Also, diverse carbanion-like species can act as nucleophiles, thus making it of general applicability.

Copper-catalyzed gem -difluoroolefination of diazo compounds with TMSCF3 via C-F bond cleavage

A novel Cu-catalyzed gem-difluoroolefination of diazo compounds is described. This transformation starts from readily available TMSCF3 and diazo compounds, via trifluoromethylation followed by C-F bond cleavage, to afford the desired 1,1-difluoroalkene products.

Fluoroanalogs of DDT: Superacidic BF3-H2O catalyzed facile synthesis of 1,1,1-trifluoro-2,2-diarylethanes and 1,1-difluoro-2,2- diarylethanes

The one-pot synthesis of 1,1,1-trifluoro- and 1,1-difluoro-2,2- diarylethanes from arenes and fluorinated hemiacetals in the BF 3-H2O system is described. The reaction is simple, clean, and convenient, eliminating the use of organic

The Kinetics of Proton and Deuteron Transfer from Ethyl bis-(4-nitrophenyl) Acetate to 1.5-Diazabicyclonon-5-ene in Polar Aprotic Solvents

The kinetics and isotope effects of the proton transfer reaction between ethyl bis-(4-nitrophenyl)acetate and 1,5.diazabicyclonon-5-ene in acetonitrile, benzonitrile, dimethyl sulphoxide, N,N-dimethylformamide and hexamethylphosphoramide solvents h

KINETICS, MECHANISM AND DEUTERIUM ISOTOPE EFFECT OF THE REACTION OF 1,1,1-TRIFLUORO-2,2-DI(4-NITROPHENYL)ETHANE WITH SODIUM PHENOLATE IN ALCOHOLS. INFLUENCE OF CROWN ETHERS AND CRYPTANDS

The reaction of 1,1,1-trifluoro-2,2-di(4-nitrophenyl)ethane with sodium phenolate in ethanol, n-propanol, iso-propanol, n-butanol, sec-butanol and t-butanol has been investigated. 1-Fluoro-1-phenoxy-2,2-di(4-nitrophenyl)ethane formed from the intermediate

Kinetics, Isotope Effects, and Mechanism of the Reaction of 1,1,1-Trifluoro-2,2-bis-(4-nitrophenyl)ethane with Piperidine and Pyrrolidine Bases in Dipolar Aprotic Solvents

The kinetics of the reaction of 1,1,1-trifluoro-2,2-bis-(4-nitrophenyl)ethane with piperidine and pyrrolidine bases in a series of solvents are reported.The reaction is complex, le

FLUORAL HEMIACETAL, A NEW REAGENT FOR AROMATIC TRIFLUORO ALKYLATION

α trifluoroalkylation of benzene was carried out in various conditions (catalyst and solvent) by using the readily available fluoral hemiacetal 1 as reagent.The good selectivity observed during the reaction was explained by the HSAB concept.

The kinetics, isotope effects, and mechanism of the reaction of 2,2-di(4-nitrophenyl)-1,1,1-trifluoroethane with alkoxide bases in alcohol solvents

The reaction between 2,2-di(4-nitrophenyl)-1,1,1-trifluoroethane and the alkoxide bases O-CH3, O-C2H5, O-nC4H9, O-CH(CH3)2 and O-C(CH3)3 in their corresponding alcohol solvents is a multistep reaction