1263145-40-9

Basic information

• Product Name: N,N-diphenyl-4-(5-methylpyridinyl-2-yl)aniline
• Synonyms: N,N-diphenyl-4-(5-methylpyridinyl-2-yl)aniline
• CAS NO: 1263145-40-9
• Molecular Weight: 336.436
• Mol File: 1263145-40-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N,N-diphenyl-4-(5-methylpyridinyl-2-yl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diphenyl-4-(5-methylpyridinyl-2-yl)aniline(1263145-40-9)
• EPA Substance Registry System: N,N-diphenyl-4-(5-methylpyridinyl-2-yl)aniline(1263145-40-9)

Safety Data

• Hazardous Substances Data: 1263145-40-9(Hazardous Substances Data)

Upstream product

• 3510-66-5 2-Bromo-5-methylpyridine 
• 201802-67-7 4-(diphenylamino)phenyl boronic acid 

Downstream Products

• 1496617-68-5 C₄₈H₃₈Cl₂N₄Pt₂ 

Relevant articles and documents

Bis-cyclometalated Ir(III) complexes with a diphenylamino group: design, synthesis, and application in oxygen sensing

A series of C?N type bis-cyclometalated Ir(III) complexes (Ir1-Ir4) with a diphenylamino group at the 4-position of the phenyl ring of 2-phenylpyridine (ppy) have been prepared and fully characterized. The influences of substituents (-H, -CH3,

Novel triphenylamine-based cyclometalated platinum(II) complexes for efficient luminescent oxygen sensing

Novel triphenylamine-based cyclometalated Pt(II) complexes containing a pyridyl moiety have been synthesized and fully characterized. The cyclometalating ligands were prepared via an efficient palladium-catalyzed ligand-free Suzuki reaction of 4-(diphenyl

Very fast, ligand-free and aerobic protocol for the synthesis of 4-aryl-substituted triphenylamine derivatives

A fast, convenient and ligand-free protocol for the synthesis of a series of 4-aryl-substituted triphenylamine derivatives by a palladium-catalysed aerobic Suzuki reaction of aryl halides with [4-(diphenylamino)phenyl]boronic acid in aqueousiPrOH is described. Importantly, both aryl bromides and heteroaryl halides afforded good to excellent yields under mild conditions. A facile, efficient and general ligand-free Suzuki reaction in aqueous iPrOH is described. Under the optimized conditions, both aryl bromides and heteroaryl halidesreacted rapidly with [4-(diphenylamino)phenyl]boronic acid, providing a series of 4-aryl-substituted triphenylamine derivatives in good to excellent yields.