42134-71-4

Basic information

• Product Name: 1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97
• Synonyms: 1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97;1,2-[Bis-(4-trifluoromethyl)phenyl]ethane 97%
• CAS NO: 42134-71-4
• Molecular Formula: C₁₆H₁₂F₆
• Molecular Weight: 318.2588
• Mol File: 42134-71-4.mol
• Article Data: 24

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97(42134-71-4)
• EPA Substance Registry System: 1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97(42134-71-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 42134-71-4(Hazardous Substances Data)

Usage

Description

1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97 is a colorless liquid chemical compound with a molecular formula of C16H12F6 and a molecular weight of 314.25 g/mol. It is commonly used as a building block or intermediate in the synthesis of various organic compounds and is derived from the reaction of 1,2-dibromoethane and 4-trifluoromethylbenzene.

Uses

Used in Pharmaceutical Industry:
1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97 is used as a key intermediate in the synthesis of various pharmaceuticals for its versatility and stability.
Used in Agrochemical Industry:
1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97 is used as a building block in the production of agrochemicals, contributing to the development of effective and stable products for agricultural applications.
Used in Specialty Chemicals Industry:
1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97 is used as an intermediate in the synthesis of specialty chemicals, providing a foundation for the creation of unique and high-quality products.
Used in Plastics and Polymers Industry:
1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97 is used in the manufacturing of plastics, polymers, and other industrial products, enhancing their properties and performance.
Overall, 1,2-[BIS-(4-TRIFLUOROMETHYL)PHENYL]ETHANE 97 is a highly pure compound with a purity of at least 97% and is widely used across various industries due to its versatility and stability.

Upstream product

• 455-19-6 4-Trifluoromethylbenzaldehyde 
• 30932-37-7 phenyl(4-(trifluoromethyl)benzyl)sulfane 
• 939-99-1 4-trifluoromethylbenzyl chloride 
• 75-65-0 tert-butyl alcohol 
• 128732-39-8 p-(trifluoromethyl)benzyl diethyl phosphate 
• 108868-46-8 1,3-Bis<4-(trifluoromethyl)phenyl>acetone 
• 42134-74-7 (E)-1,2-bis(4-trifluoromethylphenyl)ethene 
• 349-95-1 4-(trifluoromethyl)benzylic alcohol 
• 98-56-6 4-chlorobenzotrifluoride 
• 402-49-3 4-bromomethyltrifluoromethylbenzene 
• 32857-62-8 4-Trifluoromethylphenylacetic acid 
• 119757-51-6 1,2-bis(4-(trifluoromethyl)phenyl)ethyne 
• 71740-33-5 N,N-dimethyl-1-(4-(trifluoromethyl)phenyl)methanamine 
• 110-83-8 cyclohexene 

Relevant articles and documents

Photochemical Organocatalytic Benzylation of Allylic C–H Bonds

We report a radical-based organocatalytic method for the direct benzylation of allylic C–H bonds. The process uses nonfunctionalized allylic substrates and readily available benzyl radical precursors and is driven by visible light. Crucial was the identification of a dithiophosphoric acid that performs two distinct catalytic roles, sequentially acting as a catalytic donor for the formation of photoactive electron donor–acceptor (EDA) complexes and then as a hydrogen atom abstractor. By mastering these orthogonal radical generation paths, the organic catalyst enables the formation of benzylic and allylic radicals, respectively, to then govern their selective coupling. The protocol was also used to design a three-component radical process, which increased the synthetic potential of the chemistry.

Iron-Based Catalyst for Borylation of Unactivated Alkyl Halides without Using Highly Basic Organometallic Reagents

The mild borylation of alkyl bromides and chlorides with bis(neopentylglycolato)diborane (B2neop2) mediated by iron-bis amide is described. The reaction proceeds with a broad substrate scope and good functional group compatibility. Moreover, sufficient ca

Use of Isopropyl Alcohol as a Reductant for Catalytic Dehydoxylative Dimerization of Benzylic Alcohols Utilizing Ti?O Bond Photohomolysis

Photohomolysis of Ti?O bonds is utilized in photocatalytic generation of titanium(III) species for dehydroxylative dimerization of benzylic alcohols under UV-light irradiation by using isopropyl alcohol (IPA) as a stoichiometric reductant. In this reaction, IPA works not as a single-electron donor as in the photo-redox catalyzed reactions but as an H-atom-donor. The reaction also proceeds under visible-light irradiation in the presence of thioglycolic acid as a ligand.