1019056-21-3

Basic information

• Product Name: dimethyl 4-(diphenylamino)phenylboronate
• Synonyms: dimethyl 4-(diphenylamino)phenylboronate
• CAS NO: 1019056-21-3
• Molecular Weight: 317.195
• Mol File: 1019056-21-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: dimethyl 4-(diphenylamino)phenylboronate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 4-(diphenylamino)phenylboronate(1019056-21-3)
• EPA Substance Registry System: dimethyl 4-(diphenylamino)phenylboronate(1019056-21-3)

Safety Data

• Hazardous Substances Data: 1019056-21-3(Hazardous Substances Data)

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 122-39-4 diphenylamine 
• 106-40-1 4-bromo-aniline 
• 121-43-7 Trimethyl borate 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 

Downstream Products

• 201802-67-7 4-(diphenylamino)phenyl boronic acid 
• 1143507-65-6 1-(4'-(diphenylamino)-[1,1'-biphenyl]-4-yl)ethanone 
• 1096156-19-2 ethyl 4'-(diphenylamino)biphenyl-4-carboxylate 
• 554458-97-8 4'-(diphenylamino)-[1,1'-biphenyl]-4-carboxylic acid 
• 1258948-07-0 1-(3',5'-dibromophenyl)-4-diphenylaminobenzene 
• 1285686-71-6 C₂₈H₂₃NO₂ 
• 1285686-72-7 C₃₃H₂₅NO₂ 
• 1285686-74-9 C₃₂H₂₉N₃O₂ 
• 1160294-75-6 1-(4'-(N,N-diphenylamino)phenyl)naphthalene 

Relevant articles and documents

Violet-blue-or pure-blue-emitting triphenylamine derivatives: Synthesis and properties

We report the synthesis and optoelectronic properties of a series of nine triphenylamine derivatives. They were synthesized by Suzuki cross-coupling reactions and characterized by elemental analysis, nuclear magnetic resonance, ultraviolet visible absorpt

Novel organic dyes with anchoring group of quinoxaline-2, 3-diol and the application in dye-sensitized solar cells

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Efficient and stable dye-sensitized solar cells based on phenothiazine sensitizers with thiophene units

Three new phenothiazine organic dyes containing thiophene, 3-(5-(3-(4-(bis(4-methoxy phenyl)amino)phenyl)-10-octyl-10H-phenothiazin-7-yl) thiophen-2-yl)-2-cyanoacrylic acid (P1), 3-(5-(3-(4-(diphenylamino)phenyl)-10- octyl-10H-phenothiazin-7-yl)thiophen-2-yl)-2-cyanoacrylic acid (P2) and 2-cyano-3-(5-(10-octyl-3-(4-(2,2-diphenylvinyl)phenyl)-10H-phenothiazin-7-yl) thiophen-2-yl) acrylic acid (P3) were designed and synthesized as sensitizers for application in dye-sensitized solar cells (DSSCs). For these dyes, the phenothiazine derivative moiety and the cyanoacetic acid take the roles of electron donor and electron acceptor, respectively. The absorption spectra, electrochemical and photovoltaic properties of P1-P3 and the cell long-term stability were extensively investigated. It was found that HOMO and LUMO energy level tuning can be conveniently accomplished by alternating the donor moiety. The DSSCs based on dye P2 showed the best photovoltaic performance: a maximum monochromatic incident photon-to-current conversion efficiency (IPCE) of 84.9%, a short-circuit photocurrent density (Jsc) of 10.84 mA cm -2, an open-circuit photovoltage (Voc) of 592 mV, and a fill factor (ff) of 0.69, corresponding to an overall conversion efficiency of 4.41% under standard global AM 1.5 solar light conditions. These results demonstrated that the DSSCs based on phenothiazine dyes could achieve both high performance and good stability.