1378024-76-0

Basic information

• Product Name: N-(4-(10H-phenothiazine-10-yl)phenyl)-4-methyl-N-(p-tolyl)aniline
• Synonyms: N-(4-(10H-phenothiazine-10-yl)phenyl)-4-methyl-N-(p-tolyl)aniline
• CAS NO: 1378024-76-0
• Molecular Weight: 470.638
• Mol File: 1378024-76-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(4-(10H-phenothiazine-10-yl)phenyl)-4-methyl-N-(p-tolyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-(10H-phenothiazine-10-yl)phenyl)-4-methyl-N-(p-tolyl)aniline(1378024-76-0)
• EPA Substance Registry System: N-(4-(10H-phenothiazine-10-yl)phenyl)-4-methyl-N-(p-tolyl)aniline(1378024-76-0)

Safety Data

• Hazardous Substances Data: 1378024-76-0(Hazardous Substances Data)

Upstream product

• 20440-95-3 N-phenyl-di-p-tolylamine 
• 92-84-2 10H-phenothiazine 
• 58047-43-1 N,N-bis(4-methylphenyl)-N-(4-iodophenyl) amine 
• 58047-42-0 4-bromo-N,N-di-p-tolylaniline 

Downstream Products

• 1378024-68-0 C₃₆H₂₇BrN₂S₂ 
• 1361587-76-9 C₅₅H₄₁N₃OS 
• 1361587-78-1 C₅₉H₄₃N₃OS₂ 
• 1361587-80-5 C₅₉H₄₃N₃OS₂ 
• 1361587-71-4 C₅₈H₄₂N₄O₂S 
• 1361587-73-6 C₆₂H₄₄N₄O₂S₂ 
• 1361587-72-5 C₆₂H₄₄N₄O₂S₂ 
• 1378025-41-2 4-(3,7-dibromo-10H-phenothiazin-10-yl)-N,N-di-p-tolylaniline 
• 1361587-81-6 C₃₃H₂₅BrN₂OS 

Relevant articles and documents

Semiconducting Polymer Dots with Dual-Enhanced NIR-IIa Fluorescence for Through-Skull Mouse-Brain Imaging

Fluorescence probes in the NIR-IIa region show drastically improved imaging owing to the reduced photon scattering and autofluorescence in biological tissues. Now, NIR-IIa polymer dots (Pdots) are developed with a dual fluorescence enhancement mechanism.

Phenothiazine derivatives as organic sensitizers for highly efficient dye-sensitized solar cells

A series of organic dyes containing a phenothiazine central unit were synthesized and were used effectively in the fabrication of dye-sensitized solar cells (DSSCs). A cyanoacrylate moiety was added at the C(3) position of the phenothiazine as an electron acceptor, and a triarylamine moiety was attached at the C(7) position as an electron donor. The DSSCs made with these dyes displayed remarkable quantum efficiency, ranging from 4.2-6.2% under an AM 1.5 solar condition (100 mW cm-2). A variety of substituents, i.e., methyl, hexyl and triphenylamino groups, were added at the N(10) of phenothiazine in order to optimize the incident photon-to-current conversion efficiency. Along the main chromophore a thiophenylene group was inserted at different positions to examine its influence on the properties of devices. The best performance was found in compound NSPt-C6, in which a hexyl group was attached at the N(10) of phenothiazine and a thiophenylene at the C(7) position. It displayed a short-circuit current (Jsc) of 14.42 mA cm -2, an open-circuit voltage (Voc) of 0.69 V, and a fill factor (ff) of 0.63, corresponding to an overall conversion efficiency of 6.22%. Their photophysical properties were analyzed with the aid of a time-dependent density functional theory (TDDFT) model with the B3LYP functional. Their photovoltaic behavior was further elucidated by the electrochemical impedance spectroscopy.