528610-00-6

Basic information

• Product Name: 4-methyl-N-(4-methylphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amine
• Synonyms: 4-methyl-N-(4-methylphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amine
• CAS NO: 528610-00-6
• Molecular Weight: 399.341
• Mol File: 528610-00-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-methyl-N-(4-methylphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-(4-methylphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amine(528610-00-6)
• EPA Substance Registry System: 4-methyl-N-(4-methylphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amine(528610-00-6)

Safety Data

• Hazardous Substances Data: 528610-00-6(Hazardous Substances Data)

Upstream product

• 106-40-1 4-bromo-aniline 
• 624-31-7 4-tolyl iodide 
• 589-87-7 1,4-bromoiodobenzene 
• 58047-42-0 4-bromo-N,N-di-p-tolylaniline 
• 73183-34-3 bis(pinacol)diborane 
• 94584-18-6 2-isopropoxy-4,4,5,5,-tetramethyl-1,3,2-dioxaborane 
• 620-93-9 di-p-tolylamine 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant articles and documents

Asymmetric push-pull small molecules with auxiliary electron-accepting unit for bulk heterojunction organic solar cells

Two small molecular donors (TPA-DPP and TPA-DPP-MDN) were designed with asymmetric push-pull structure, namely, donor-acceptor (D-A) and donor-acceptor-acceptor (D-A-A) systems. They were synthesized and investigated by thermogravimetric analysis, UV–vis spectra, X-ray diffraction, density functional theory (DFT) calculation, electrochemical and the photovoltaic (PV) measurement. The D-A-A architecture (TPA-DPP-MDN) exhibited lower highest occupied molecular orbital (HOMO) of –5.18 eV, narrower optical band gap of 1.52 eV, better thermal stability and higher degree of ordered aggregation than these of the D-A system (TPA-DPP). TPA-DPP-MDN based PV device showed better performance with higher open-circuit voltage (VOC) and short-circuit current density (JSC) than these of TPA-DPP based PV devices due to the low-lying HOMO level and wide spectral absorption range of TPA-DPP-MDN.

Additional donor bridge as a design approach for multi-anchoring dyes for highly efficient dye-sensitized solar cells

This work presents an approach for designing efficient multi-anchoring dyes for dye-sensitized solar cells by using additional donor as a bridging group between donor–acceptor (D–A) side arms. With triarylamine as the additional donor and phenothiazine-cyanoacrylic acid as the D–A side arm, the multi-anchoring dyes exhibited higher molar extinction coefficients in the intramolecular charge transfer bands, less dye aggregation on the TiO2 surface, and better DSSC performance than that of the mono-anchoring reference dye. The best cell efficiency of 7.06% was obtained from the di-anchoring dye with two additional donor units T2P2 showing the largest charge recombination resistance of 99.7 Ω, open circuit voltage of 0.83 V, and short-circuit photocurrent density of 12.72 mA cm?2. The improvement in performance of the designed dyes suggests that additional donor is a potential bridging group for efficient multi-anchoring sensitizers.

Synthesis of some green dopants for OLEDs based on arylamine 2,3-disubstituted bithiophene derivatives

A series of green dopants based on 2,2-diphenylvinyl end-capped bithiophene and three different arylamine moieties (9-phenylcarbazole, triphenylamine, and N,N'-di-(ptolyl) benzeneamine) were successfully synthesized by the Suzuki and Wittig coupling react