1307862-95-8

Basic information

• Product Name: C₁₈H₁₆F₂O₂
• Synonyms: C₁₈H₁₆F₂O₂
• CAS NO: 1307862-95-8
• Molecular Weight: 302.321
• Mol File: 1307862-95-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₈H₁₆F₂O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₁₆F₂O₂(1307862-95-8)
• EPA Substance Registry System: C₁₈H₁₆F₂O₂(1307862-95-8)

Safety Data

• Hazardous Substances Data: 1307862-95-8(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 342-23-4 bis(fluorophenyl)methanone 

Downstream Products

• 1307863-34-8 ((2R,3R)-3-chloro-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone 
• 1307863-29-1 ((2S,3S)-3-chloro-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone 
• 1307863-20-2 ((2R,3R)-3-bromo-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone 
• 1307863-08-6 ((2S,3S)-3-bromo-2-(2-fluorophenyl)-tetrahydro-2H-pyran-2-yl)-2-fluorophenylmethanone 

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.