143880-83-5

Basic information

• Product Name: (R)-(2,4-dichlorophenyl)(phenyl)methanol
• Synonyms: (R)-(2,4-dichlorophenyl)(phenyl)methanol
• CAS NO: 143880-83-5
• Molecular Weight: 253.128
• Mol File: 143880-83-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (R)-(2,4-dichlorophenyl)(phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(2,4-dichlorophenyl)(phenyl)methanol(143880-83-5)
• EPA Substance Registry System: (R)-(2,4-dichlorophenyl)(phenyl)methanol(143880-83-5)

Safety Data

• Hazardous Substances Data: 143880-83-5(Hazardous Substances Data)

Upstream product

• 19811-05-3 2,4-dichlorobenzophenone 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 98-80-6 phenylboronic acid 
• 3262-89-3 triphenylboroxine 

Relevant articles and documents

Axially chiral C2-symmetric N-heterocyclic carbene (NHC) palladium complexes-catalyzed asymmetric arylation of aldehydes with arylboronic acids

Chiral C2-symmetric N-heterocyclic carbene (NHC) palladium diaquo complexes 5ac and the chiral C2-symmetric NHC-palladium complexes 5d and 5e prepared from (R)-BINAM or H8-(R)-BINAM could be used as the catalysts for the e

Asymmetric Hydrogenation of Polysubstituted Aromatic Ketones Catalyzed by the DIPSkewphos/PICA Derivative–Ruthenium(II) Complexes

The DIPSkewphos/PICA derivative-Ru(II) complexes catalyzed asymmetric hydrogenation of significantly sterically hindered 2’,3’,4’,5’,6’-pentamethylacetophenone, which was not reduced with NaBH4 at 25 °C, with a substrate-to-catalyst molar ratio

Catalyzed asymmetric aryl transfer reactions to aldehydes with boroxines as aryl source

Asymmetric aryl transfer of triphenylboroxin to a set of aryl aldehydes has been carried out in the presence of chiral amino alcohols derived from (S)-proline with high enantioselectivity. Substituted phenyl boroxins were also used as aryl source in asymmetric arylation of benzaldehyde.