1007834-86-7

Basic information

• Product Name: (S)-1-fluoro-4-(1-(4-methoxyphenyl)ethyl)benzene
• Synonyms: (S)-1-fluoro-4-(1-(4-methoxyphenyl)ethyl)benzene
• CAS NO: 1007834-86-7
• Molecular Weight: 230.282
• Mol File: 1007834-86-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-1-fluoro-4-(1-(4-methoxyphenyl)ethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-fluoro-4-(1-(4-methoxyphenyl)ethyl)benzene(1007834-86-7)
• EPA Substance Registry System: (S)-1-fluoro-4-(1-(4-methoxyphenyl)ethyl)benzene(1007834-86-7)

Safety Data

• Hazardous Substances Data: 1007834-86-7(Hazardous Substances Data)

Upstream product

• 456-16-6 1-(1-chloroethyl)-4-fluorobenzene 
• 1007834-93-6 C₁₆H₁₅FO₂ 
• 405-99-2 para-fluorostyrene 
• 5720-07-0 4-methoxyphenylboronic acid 

Relevant articles and documents

Nickel-catalyzed Enantioselective Hydroarylation and Hydroalkenylation of Styrenes

We have developed a Ni-catalyzed enantioselective hydroarylation of styrenes with arylboronic acids using MeOH as the hydrogen source, providing an efficient method to access 1,1-diarylalkanes, which are essential structural units in many biologically active compounds. In addition, Ni-catalyzed enantioselective hydrovinylation of styrenes with vinylboronic acids is also realized with good yields and enantioselectivities. The synthetic utility was demonstrated by the efficient synthesis of (R)-(-)-ibuprofen.

Enantioselective preparation of 1,1-diarylethanes: Aldehydes as removable steering groups for asymmetric synthesis

Cut it out! Convenient procedures have been delineated for the synthesis of optically active, functionalized 1,1-diaryl-ethanes by decarbonylation of β,β-diaryl-propionaldehydes. The process can be conducted as a one-pot 1,4-addition/decarbonylation sequence. Aldehydes are used as removable steering groups in this new strategy for the preparation of optically active building blocks. (Chemical Equation Presented)