194149-25-2

Basic information

• Product Name: [bis-(3,5-dimethylphenyl)](diethylamino)phosphine
• Synonyms: [bis-(3,5-dimethylphenyl)](diethylamino)phosphine
• CAS NO: 194149-25-2
• Molecular Weight: 313.423
• Mol File: 194149-25-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: [bis-(3,5-dimethylphenyl)](diethylamino)phosphine(CAS DataBase Reference)
• NIST Chemistry Reference: [bis-(3,5-dimethylphenyl)](diethylamino)phosphine(194149-25-2)
• EPA Substance Registry System: [bis-(3,5-dimethylphenyl)](diethylamino)phosphine(194149-25-2)

Safety Data

• Hazardous Substances Data: 194149-25-2(Hazardous Substances Data)

Upstream product

• 1069-08-5 diethylphosphoramidous dichloride 
• 34696-73-6 3,5-dimethyphenylmagnesium bromide 

Downstream Products

• 660-68-4 diethyl amine hydrochloride 
• 74289-57-9 bis-(3,5-dimethylphenyl)chlorophosphine 
• 158214-06-3 methyl 2,6-di-O-benzoyl-3,4-bis-O-(bis(3,5-dimethylphenyl)phosphino)-α-D-glucopyranoside 
• 137219-83-1 (3-(chloro(3,5-dimethylphenyl)phosphoryl)-5-methylphenyl)methylium 
• 137219-84-2 2,2'-bis[di-(3,5-dimethylphenyl)phosphoryl]-1,1'-binaphthyl 
• 137219-86-4 2,2'-bis[di(3,5-dimethylphenyl)phosphino]-1,1'-binaphthyl 

Relevant articles and documents

Enantioselective hydrogenation of α-dehydroamino acid esters catalyzed by rhodium complexes with chiral bisaminophosphine ligands

A highly efficient strategy for the synthesis of a series of chiral bisaminophosphine ligands was well established with several remarkable features. The synthetic utility of these ligands was explored for rhodium-catalyzed asymmetric hydrogenations of α-d

Chiral diphosphorus compounds and their transition metal complexes

The present invention relates to chiral diphosphorus compounds and their transition metal complexes, to a process for preparing chiral diphosphorus compounds and their transition metal complexes and also to their use in asymmetric syntheses.

Stereospecific deoxygenation of phosphine oxides with retention of configuration using triphenylphosphine or triethyl phosphite as an oxygen acceptor

(Chemical Equation Presented) A new protocol for deoxygenation of various phosphine oxides with retention of configuration is described. The advantage of the new method includes milder conditions and considerably shortened reaction times. Mechanistic studies about the oxygen transfer between the starting phosphine oxide and the sacrificial triphenylphosphine are also presented.