3112-01-4

Usage

Uses

Used in Pharmaceutical Industry:
3-Phenylbenzoylmethide is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and composition make it a valuable building block in the development of new drugs and therapeutic agents.
Used in Chemical Research:
3-Phenylbenzoylmethide is used as a research compound in the field of organic chemistry. Its properties and reactivity can be studied to gain insights into the behavior of similar compounds and to develop new synthetic methods and strategies.
Used in Industrial Chemistry:
3-Phenylbenzoylmethide is used as a specialty chemical in various industrial processes. Its unique properties may be harnessed to improve the performance of certain materials or to develop new products with specific applications in various industries.

Upstream product

• 595-90-4 tetraphenyltin(IV) 
• 2142-63-4 1-(3-Bromophenyl)ethanone 
• 591-50-4 iodobenzene 
• 214360-49-3 1-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-ethanone 
• 99-90-1 para-bromoacetophenone 
• 98-80-6 phenylboronic acid 
• 603-33-8 triphenylbismuthane 
• 138313-22-1 3-acetylphenyl trifluoromethanesulfonate 

Downstream Products

• 23948-77-8 1,1'-biphenyl-3-ylacetic acid 
• 110826-97-6 m-phenyl-α-methylbenzylamine 
• 1314023-84-1 ethyl 5-(1,1'-biphenyl-3-yl)-isoxazole-3-carboxylate 
• 1314023-87-4 5-(1,1'-biphenyl-3-yl)-isoxazole-3-carboxylic acid 
• 1314024-02-6 N-(2-(benzo[d][1,3]dioxol-5-yl)ethyl)-5-(1,1'-biphenyl-3-yl)-isoxazole-3-carboxamide 
• 1026960-36-0 3-[3-biphenyl-3-yl-1-(3-trifluoromethyl-phenyl)-1H-pyrazol-4-yl]-acrylic acid 
• 19163-31-6 1-(biphenyl-4-yl)-3-(5-phenylthiophen-2-yl)prop-2-en-1-one 
• 1198168-44-3 N-(2-(biphenyl-3-yl)imidazo[1,2-a]pyridin-8-yl)pyrazine-2-carboxamide 
• 1198170-78-3 2-(biphenyl-3-yl)-8-nitroimidazo[1,2-a]pyridine 
• 1198170-80-7 2-(biphenyl-3-yl)imidazo[1,2-a]pyridin-8-amine 

Relevant academic research and scientific papers

Electron-deficient olefin ligands enable generation of quaternary carbons by Ni-catalyzed cross-coupling

A Ni-catalyzed Negishi cross-coupling with 1,1-disubstituted styrenyl aziridines has been developed. This method delivers valuable β-substituted phenethylamines via a challenging reductive elimination that affords a quaternary carbon. A novel electron-deficient olefin ligand, Fro-DO, proved crucial for achieving high rates and chemoselectivity for C-C bond formation over β-H elimination. This ligand is easy to access, is stable, and presents a modular framework for reaction discovery and optimization. We expect that these attributes, combined with the fact that the ligands impart distinct electronic properties to a metal, will support the invention of new transformations not previously possible using established ligands.

Formation of cine-substitution products in the Suzuki-Miyaura cross-coupling reaction catalyzed by dinuclear palladium complexes

The Suzuki-Miyaura coupling reaction catalyzed by dinuclear palladium complexes gave cine-substitution products along with ordinary ipso-substitution products. In the reaction in (D6)benzene, the ipso position of the cine-substitution product was highly deuterated. The H/D exchange also occurred in various positions of benzene rings. Copyright

Direct conversion of arylamines to pinacol boronates: A metal-free borylation process

Leave the metal out: Arylboronates are produced In moderate to good yields by direct borylation of readily available aryl amines (see scheme). The reaction can be carried out under air at room temperature and transition-metal catalysis is not required. The boronate products can be used without purification in SuzukiMiyaura cross-coupling reactions. Chemical equation representation

Pd(PPh3)4-PEG 400 catalyzed protocol for the atom-efficient stille cross-coupling reaction of organotin with aryl bromides

(Chemical Equation Presented) Aryl bromides (4 equiv) were coupled efficiently with organotin (1 equiv) in an atom-efficient way using the tetra(triphenylphosphine)palladium/polyethylene glycol 400 (Pd(PPh 3)4/PEG 400) catalytic syst

A new palladium catalyzed protocol for atom-efficient cross-coupling reactions of?triarylbismuths with aryl halides and triflates

A new palladium catalyzed protocol for an atom-efficient cross-coupling reaction of triarylbismuths with aryl halides and triflates has been described. The palladium catalytic system with Cs2CO3 base was found to be very efficient in DMA solvent to furnish excellent yields of cross-coupled functionalized biaryls in short reaction times.