121197-53-3

Basic information

• Product Name: (C₆H₅)2PONCHC₁₀H₇
• Synonyms: (C₆H₅)2PONCHC₁₀H₇
• CAS NO: 121197-53-3
• Molecular Weight: 355.376
• Mol File: 121197-53-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (C₆H₅)2PONCHC₁₀H₇(CAS DataBase Reference)
• NIST Chemistry Reference: (C₆H₅)2PONCHC₁₀H₇(121197-53-3)
• EPA Substance Registry System: (C₆H₅)2PONCHC₁₀H₇(121197-53-3)

Safety Data

• Hazardous Substances Data: 121197-53-3(Hazardous Substances Data)

Upstream product

• 1499-21-4 Diphenylphosphinic chloride 
• 1707-03-5 diphenyl-phosphinic acid 
• 5994-87-6 diphenylphosphinamide 
• 66-77-3 1-naphthaldehyde 
• 18856-91-2 C₁₂H₁₀NO₂PS 
• 13504-46-6 α-naphthalenecarboaldoxime 
• 1079-66-9 chloro-diphenylphosphine 

Downstream Products

• 1215194-85-6 N-(2-(9H-fluoren-9-ylideneamino)-1-(naphthalen-1-yl)ethyl)-P,P-diphenylphosphinic amide 
• 121197-62-4 2-(diphenylphosphinoyl)-3-(1-naphthyl)oxaziridine 

Relevant articles and documents

AN EFFICIENT METHOD FOR THE PREPARATION OF N-PHOSPHINOYL AND N-SULPHONYL IMINES DIRECTLY FROM AROMATIC ALDEHYDES

Reaction of phosphinamides and sulphonamides with aromatic aldehydes at 0 deg C in the presence of titanium tetrachloride and triethylamine provides a simple one-step preparation of N-phosphinoyl and N-sulphonyl imines.

Highly Diastereo- and Enantioselective Cu-Catalyzed Borylative Coupling of 1,3-Dienes and Aldimines

A Cu-catalyzed diastereo- and enantioselective borylative coupling reaction of 1,3-dienes with imines was realized. Branched homoallylic amines are readily prepared in a syn-selective manner with high regio-, diastereo- and enantioselectivity. Moreover, t

Synthesis of N-diphenylphosphinoylimines using the Kresze reaction

The synthesis of N-diphenylphosphinoylimines involving the treatment of aldehydes with P,P-diphenyl N-sulfmylphosphoramidate (Ph2P(O)NSO) is described. The reagent is prepared from P,P-diphenylphosphinic amide, thionyl chloride, and imidazole.