130065-37-1

Basic information

• Product Name: (S)-1-(4-(1-phenylethyl)phenyl)ethan-1-one
• Synonyms: (S)-1-(4-(1-phenylethyl)phenyl)ethan-1-one
• CAS NO: 130065-37-1
• Molecular Weight: 224.302
• Mol File: 130065-37-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (S)-1-(4-(1-phenylethyl)phenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(4-(1-phenylethyl)phenyl)ethan-1-one(130065-37-1)
• EPA Substance Registry System: (S)-1-(4-(1-phenylethyl)phenyl)ethan-1-one(130065-37-1)

Safety Data

• Hazardous Substances Data: 130065-37-1(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 109613-00-5 4-acetophenyl triflate 
• 149104-90-5 4-acetylphenylboronic acid 
• 99-90-1 para-bromoacetophenone 
• 672-65-1 (1-chloroethyl)benzene 
• 13329-40-3 4-Iodoacetophenone 
• 174090-36-9 4,4,5,5-tetramethyl-2-(1-phenyl-ethyl)-[1,3,2]dioxaborolane 
• 257298-92-3 (R)-4,4,5,5-tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolane 

Relevant articles and documents

Nickel-Catalyzed Regiodivergent Reductive Hydroarylation of Styrenes

We report a ligand-controlled nickel-catalyzed reductive hydroarylation of styrenes with predictable and controllable regioselectivity. With a diamine ligand, the reaction produces selective linear hydroarylation products. Alternatively, with a chiral PyrOx ligand, branch-selective enantioenriched 1,1-diarylalkane products are obtained. Preliminary mechanistic results are consistent with a reductive Heck process.

Enantioselective Reductive Cross-Coupling of Aryl/Alkenyl Bromides with Benzylic Chlorides via Photoredox/Biimidazoline Nickel Dual Catalysis

The asymmetric reductive arylation and alkenylation of benzylic chloride under photoredox/nickel dual catalysis using chiral biimidazoline (BiIm) ligand is reported to access 1,1-diaryl alkanes and aryl allylic compounds with good yield as well as stereo-

Highly chemoselective and enantiospecific Suzuki-Miyaura cross-couplings of benzylic organoboronic esters

The use of potassium carbonate in addition to silver oxide is shown to increase the enantiospecificity of the Suzuki-Miyaura cross-coupling reaction of chiral secondary benzylic boronic esters. From mechanistic studies, it is shown that the reaction is co