144147-62-6

Basic information

• Product Name: Cyclohexanone, 2-[(4-fluorophenyl)methyl]-
• CAS NO: 144147-62-6
• Molecular Formula: C13H15FO
• Molecular Weight: 206.26
• Mol File: 144147-62-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-[(4-fluorophenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-[(4-fluorophenyl)methyl]-(144147-62-6)
• EPA Substance Registry System: Cyclohexanone, 2-[(4-fluorophenyl)methyl]-(144147-62-6)

Safety Data

• Hazardous Substances Data: 144147-62-6(Hazardous Substances Data)

Upstream product

• 732306-64-8 bis(4-fluorophenyl)iodonium triflate 
• 39209-07-9 2-methylcyclohexanone O-methyl oxime 
• 502-00-1 p-fluorobenzyl acetate 
• 80522-46-9 1-triisopropylsiloxy-1-cyclohexene 
• 111729-74-9 (E)-2-(4-fluoro-phenylmethylene)-cyclohexanone 
• 459-57-4 4-fluorobenzaldehyde 
• 108-94-1 cyclohexanone 
• 121045-02-1 (E)-2-(4-fluoro-phenylmethylene)-cyclohexanol 

Downstream Products

• 144147-73-9 2-(2,2-Dimethoxy-acetyl)-6-(4-fluoro-benzyl)-cyclohexanone 
• 144149-41-7 (E)-3-[7-(4-Fluoro-benzyl)-2-(4-fluoro-phenyl)-4,5,6,7-tetrahydro-2H-indazol-3-yl]-propenal 
• 144148-18-5 7-(4-Fluoro-benzyl)-2-(4-fluoro-phenyl)-4,5,6,7-tetrahydro-2H-indazole-3-carbaldehyde 

Relevant articles and documents

β-Arylation of oxime ethers using diaryliodonium salts through activation of inert C(sp 3)-H bonds using a palladium catalyst

An efficient method of selective β-arylation of oxime ethers was realized by using a palladium catalyst with diaryliodonium salts as the key arylation reagents. The reaction proceeded smoothly through the activation of inert C(sp3)-H bonds to give corresponding ketones and aldehydes. This convenient procedure can be successfully applied to construct new C(sp3)-C(sp2) bonds on a number of complex molecules derived from natural products and thus serves as a practical synthetic tool for direct late-stage C(sp3)-H functionalization.

THE EFFECTS OF SUBSTITUENS AND SOLVENT POLARITY ON PHOTOCHEMICAL SIGMATROPIC SHIFTS. EXPERIMENTAL EVIDENCE IN FAVOUR OF THE OCCURRENCE OF SUDDEN POLARIZATION IN ACYCLIC ALKENES

Furher experimental evidence regarding the occurence of sudden polarization in acyclic alkenes is presented.It is shown that the yield of formation of the product derived from an intramolecular photochemical -OH shift in the 1 is dependent only on the polarity of the solvent employed.This result could be well explained in terms of a stabilization of the zwitterionic intermediate formed upon irradiation of 1 by reorientation polarization of the dipole solvent molecules.Besides this, it was found that replacement of the alkyl group at the terminal carbon atom of the C3-C9 exocyclic double bond in 1 by a phenyl substituent led to the occurence of a photochemical -H shift.This directive effect of the substituents at the exocyclic double bond could be well explained on the basis of the sudden polarization model.