1307863-29-1

Basic information

• Product Name: ((2S,3S)-3-chloro-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone
• Synonyms: ((2S,3S)-3-chloro-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone
• CAS NO: 1307863-29-1
• Molecular Weight: 336.766
• Mol File: 1307863-29-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((2S,3S)-3-chloro-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone(CAS DataBase Reference)
• NIST Chemistry Reference: ((2S,3S)-3-chloro-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone(1307863-29-1)
• EPA Substance Registry System: ((2S,3S)-3-chloro-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone(1307863-29-1)

Safety Data

• Hazardous Substances Data: 1307863-29-1(Hazardous Substances Data)

Upstream product

• 342-23-4 bis(fluorophenyl)methanone 
• 1307862-95-8 C₁₈H₁₆F₂O₂ 

Relevant articles and documents

Organocatalytic asymmetric halogenation/semipinacol rearrangement: Highly efficient synthesis of chiral α-oxa-quaternary β-haloketones

A novel asymmetric halogenation/semipinacol rearrangement reaction catalyzed by cinchona alkaloid derivatives was developed. Two types of β-haloketones (X = Br, Cl) were obtained with up to 95% yield and 99% enantiomeric excess. The desired (+) and (-) enantiomers of the β-haloketones were readily obtained.