1263145-39-6

Basic information

• Product Name: 4-(5-fluoropyridin-2-yl)-N,N-diphenylaniline
• Synonyms: 4-(5-fluoropyridin-2-yl)-N,N-diphenylaniline
• CAS NO: 1263145-39-6
• Molecular Weight: 340.4
• Mol File: 1263145-39-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-(5-fluoropyridin-2-yl)-N,N-diphenylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(5-fluoropyridin-2-yl)-N,N-diphenylaniline(1263145-39-6)
• EPA Substance Registry System: 4-(5-fluoropyridin-2-yl)-N,N-diphenylaniline(1263145-39-6)

Safety Data

• Hazardous Substances Data: 1263145-39-6(Hazardous Substances Data)

Upstream product

• 41404-58-4 2-bromo-5-fluoropyridine 
• 201802-67-7 4-(diphenylamino)phenyl boronic acid 

Downstream Products

• 1496617-69-6 C₄₆H₃₂Cl₂F₂N₄Pt₂ 

Relevant articles and documents

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

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,

Palladium-catalyzed ligand-free and aqueous Suzuki reaction for the construction of (hetero)aryl-substituted triphenylamine derivatives

This paper reports an efficient synthesis of triphenylamine (TPA) derivatives via a palladium-catalyzed Suzuki reaction of (hetero)aryl halides with 4-(diphenylamino)phenylboronic acid (DPBA) in aqueous ethanol under aerobic and ligand-free conditions. Heteroaryl halides, namely pyridyl bromides, quinolyl bromides, pyrimidinyl bromides, 2-chloropyrazine and sulfur-containing heteroaryl bromides, could react smoothly with DPBA, affording good to excellent yields under mild conditions. In addition, aryl bromides were also successfully employed in the cross-couplings with DPBA and furnished the products in high yields at room temperature. The cross-coupling of 4-bromobenzonitrile with DPBA gave the desired product in a quantitative yield within 2 min, resulting in a TOF up to 5820 h-1.