890415-62-0

Basic information

• Product Name: (+)-1-(N-benzylamino)-1-(4-pyridyl)-(S)-methyl-tert-butylphenyl-(S)-phosphine oxide
• CAS NO: 890415-62-0
• Molecular Weight: 378.454
• Mol File: 890415-62-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+)-1-(N-benzylamino)-1-(4-pyridyl)-(S)-methyl-tert-butylphenyl-(S)-phosphine oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-1-(N-benzylamino)-1-(4-pyridyl)-(S)-methyl-tert-butylphenyl-(S)-phosphine oxide(890415-62-0)
• EPA Substance Registry System: (+)-1-(N-benzylamino)-1-(4-pyridyl)-(S)-methyl-tert-butylphenyl-(S)-phosphine oxide(890415-62-0)

Safety Data

• Hazardous Substances Data: 890415-62-0(Hazardous Substances Data)

Upstream product

• 72954-83-7 N-<(pyridin-4-yl)methylidene>benzylamine 
• 82945-11-7 (R_p)-t-butyl(phenyl)phosphine oxide 
• 100-46-9 benzylamine 
• 872-85-5 pyridine-4-carbaldehyde 

Downstream Products

• 85656-12-8 tert-butylphenylphosphinic acid methyl ester 
• 82945-11-7 (R_p)-t-butyl(phenyl)phosphine oxide 
• 73325-67-4 4-<(N-benzylamino)methyl>pyridine 
• 4923-86-8 t-butyl(phenyl)phosphinic acid 

Relevant articles and documents

Aminophosphine oxides in a pyridine series. Studies on the cleavage of pyridine-2- and pyridine-4-yl-(N-benzylamino)-methyldiphenylphosphine oxides in acidic solutions

The synthesis and reactions of 1-(N-benzylamino)-1-(2-pyridyl)- and 1-(N-benzylamino)-1-(4-pyridyl)-methyldiphenylphosphine oxides are described. It was found that these compounds were exceptionally easy to cleave in aqueous sulfuric acid solutions to form diphenylphosphinic acid and the corresponding N-(pyridylmethyl)-benzylamines. The structure of a single diastereoisomer, that is, the (R)-(+)-1-[N-(α-methylbenzylamino)]-1-(4-pyridyl)-(S)-methyldiphen ylphosphine oxide was determined by X-ray crystallography. The acidic alcoholysis of the selected model chiral pyridine aminophosphine oxides was investigated by means of 31P NMR spectroscopy. The cleavage kinetics were also studied. On the basis of the obtained results, a mechanism of the cleavage was formulated.