1296883-60-7

Basic information

• Product Name: bis(2-isopropylaminophenyl)amine
• Synonyms: bis(2-isopropylaminophenyl)amine
• CAS NO: 1296883-60-7
• Molecular Weight: 283.417
• Mol File: 1296883-60-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: bis(2-isopropylaminophenyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: bis(2-isopropylaminophenyl)amine(1296883-60-7)
• EPA Substance Registry System: bis(2-isopropylaminophenyl)amine(1296883-60-7)

Safety Data

• Hazardous Substances Data: 1296883-60-7(Hazardous Substances Data)

Upstream product

• 38919-26-5 bis(2-aminophenyl)amine 
• 67-64-1 acetone 
• 122-39-4 diphenylamine 
• 1493-27-2 ortho-nitrofluorobenzene 
• 88-74-4 2-nitro-aniline 
• 18264-71-6 bis(2-nitrophenyl)amine 

Relevant articles and documents

Reversible intermolecular E-H oxidative addition to a geometrically deformed and structurally dynamic phosphorous triamide

The synthesis and reactivity of geometrically constrained tricoordinate phosphorus (σ3-P) compounds supported by tridentate triamide chelates (N[o-NR-C6H4]23-; R = Me or iPr) are reported.

A structure-activity study of Ni-catalyzed alkyl-alkyl kumada coupling. Improved catalysts for coupling of secondary alkyl halides

A structureactivity study was carried out for Ni catalyzed alkylalkyl Kumada-type cross coupling reactions. A series of new nickel(II) complexes including those with tridentate pincer bis(amino)amide ligands (RN2N) and those with bidentate mixed amino-amide ligands (RNN) were synthesized and structurally characterized. The coordination geometries of these complexes range from square planar, tetrahedral, to square pyramidal. The complexes had been examined as precatalysts for cross coupling of nonactivated alkyl halides, particularly secondary alkyl iodides, with alkyl Grignard reagents. Comparison was made to the results obtained with the previously reported Ni pincer complex [( MeN2N)NiCl]. A transmetalation site in the precatalysts is necessary for the catalysis. The coordination geometries and spin-states of the precatalysts have a small or no influence. The work led to the discovery of several well-defined Ni catalysts that are significantly more active and efficient than the pincer complex [(MeN2N)NiCl] for the coupling of secondary alkyl halides. The best two catalysts are [(HNN)Ni(PPh3)Cl] and [(HNN)Ni(2,4-lutidine)Cl]. The improved activity and efficiency was attributed to the fact that phosphine and lutidine ligands in these complexes can dissociate from the Ni center during catalysis. The activation of alkyl halides was shown to proceed via a radical mechanism.