98837-46-8

Basic information

• Product Name: N-benzylidenediphenylphosphinamide
• Synonyms: N-benzylidenediphenylphosphinamide
• CAS NO: 98837-46-8
• Molecular Weight: 305.316
• Mol File: 98837-46-8.mol
• Article Data: 33

Chemical Properties

• CAS DataBase Reference: N-benzylidenediphenylphosphinamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzylidenediphenylphosphinamide(98837-46-8)
• EPA Substance Registry System: N-benzylidenediphenylphosphinamide(98837-46-8)

Safety Data

• Hazardous Substances Data: 98837-46-8(Hazardous Substances Data)

Upstream product

• 1079-66-9 chloro-diphenylphosphine 
• 932-90-1 Benzaldoxime 
• 27127-08-8 N-benzyl-P,P-diphenylphosphinic amide 
• 5994-87-6 diphenylphosphinamide 
• 100-52-7 benzaldehyde 
• 1499-21-4 Diphenylphosphinic chloride 
• 18856-91-2 C₁₂H₁₀NO₂PS 
• 932-90-1 syn-benzaldehyde oxime 
• 774-48-1 (diethoxymethyl)benzene 

Downstream Products

• 122167-14-0 1-Diphenylphosphinylamino-1-phenyl-methanthiophosphonsaeure-O,O-diethylester 
• 106651-16-5 N-(1-phenylpropyl)-diphenylphosphinamide 
• 106651-15-4 (S)-N-(1-phenylpropyl)-P,P-diphenylphosphinamide 
• 67764-54-9 N-(cyano(phenyl)methyl)-P,P-diphenylphosphinic amide 
• 154675-31-7 N-[1-(phenyl)propyl]-P,P-diphenylphosphinoylamide 
• 67764-56-1 (RS)-N-(1-phenylethyl)-P,P-diphenylphosphinamide 
• 807610-78-2 N-(2-Nitro-1-phenylethyl)-P,P-diphenylphosphinic amide 
• 441012-04-0 (S)-(-)-N-(2-nitro-1-phenylethyl)diphenylphosphine amide 
• 349451-17-8 (E)-N-(1-phenylhept-2-enyl)-P,P-diphenylphosphinamide 

Relevant articles and documents

Ni(0)-Catalyzed Three-Component Coupling Reaction of Tetrafluoroethylene and N-Sulfonyl-Substituted Imines with Silanes via Aza-Nickelacycles

A nickel-catalyzed three-component coupling reaction of tetrafluoroethylene (TFE) and N-sulfonyl-substituted imines with silanes that furnishes a variety of fluorine-containing amines is disclosed. Stoichiometric experiments revealed that the aza-nickelac

Enantioselective Synthesis of anti-1,2-Diamines by Cu-Catalyzed Reductive Couplings of Azadienes with Aldimines and Ketimines

Here we report highly efficient and chemoselective azadiene-imine reductive couplings catalyzed by (Ph-BPE)Cu-H that afford anti-1,2-diamines. In all cases, reactions take place with either aldimine or ketimine electrophiles to deliver a single diastereom

Single or Synergistic Kinetic Resolutions of Chiral Allylalanes: Two Complementary Routes for the Asymmetric Synthesis of Syn Homoallylamines

Two strategies based on kinetic resolution(s) of chiral alanes and providing enantioenriched syn homoallylamines are reported. The first implies a single kinetic resolution of the alane using camphor; the second requires two sequential kinetic resolutions using the synergistic combination of (-)-camphor/(R)-tert-butylsulfinamide-derived imines. This syn selectivity, specific to the use of allyaluminum, opens the way to the preparation of valuable building blocks as illustrated by the synthesis of (+)-epilupinamine.