1229-68-1

Usage

Uses

Used in Pharmaceutical Industry:
1-(2,2-diphenylethenyl)-2-fluorobenzene is used as a starting material for the synthesis of complex organic molecules, particularly in the pharmaceutical industry. Its unique structure and properties contribute to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
1-(2,2-diphenylethenyl)-2-fluorobenzene is used as a building block in the production of agrochemicals. Its chemical properties allow for the creation of compounds that can be utilized in the development of pesticides, herbicides, and other agricultural products.
Used in Specialty Chemicals:
1-(2,2-diphenylethenyl)-2-fluorobenzene is also used in the production of specialty chemicals, which are tailored for specific applications and industries. Its unique properties make it a valuable component in the development of these specialized compounds.
Used in Research and Development:
1-(2,2-diphenylethenyl)-2-fluorobenzene is employed in research and development processes to create new materials and compounds with potential industrial and commercial applications. Its unique structure and properties make it an essential tool in the discovery and innovation of novel chemical entities.

Upstream product

• 2023-52-1 1,1-Diphenyl-2--aethanol 
• 446-52-6 2-Fluorobenzaldehyde 
• 17507-57-2 (diphenylphosphinyl)phenyldiazomethane 
• 588-68-1 1,2-di(benzylidene)hydrazine 
• 27329-60-8 diethyl (diphenylmethyl)phosphonate 
• 345-35-7 2-fluorobenzyl chloride 

Downstream Products

• 796-12-3 1-Brom-1-(2-fluor-phenyl)-2,2-diphenyl-aethylen 

Relevant academic research and scientific papers

Microwave-assisted periselective annulation of triarylphosphenes with aldehydes and ketones

The reaction of diazo(aryl)methyl(diaryl)phosphine oxides with aldehydes and ketones generates benzo-δ-phosphinolactones in low to good yields with 1,1-diarylalk-1-enes as byproducts under microwave irradiation. Diazo(aryl)methyl(diaryl)phosphine oxides first undergo a Wolff rearrangement to form diaryl(aryl)phosphenes, which further react with aldehydes and ketones to afford benzo-δ-phosphinolactones and β-phosphinolactones. The latter are unstable under heating and fragment into the corresponding 1,1-diarylalk-1-enes and arylphosphine dioxides under reaction conditions. The arylphosphine dioxides become arylphosphonic acids during workup. The periselectivity in the annulation shows that the reaction of diaryl(aryl)phosphenes with most aldehydes and ketones favors phosphene phenyl participation in (4 + 2) annulation(2 + 2) annulation. This journal is

Electrochemical Aziridination by Alkene Activation Using a Sulfamate as the Nitrogen Source

The first direct aziridination of triaryl-substituted alkenes was achieved by means of an electrochemical process that could extend to multisubstituted styrenes. Specifically, hexafluoroisopropanol sulfamate was used as a nucleophilic nitrogen source. Mechanistic experiments suggest that this electrochemical process proceeds by stepwise formation of two C?N bonds through reactions between cationic carbon species and the sulfamate.