1404053-06-0

Basic information

• Product Name: N,N-diphenyl-4-[2-[4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)phenyl]ethenyl]-benzenamine
• Synonyms: N,N-diphenyl-4-[2-[4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)phenyl]ethenyl]-benzenamine
• CAS NO: 1404053-06-0
• Molecular Weight: 473.423
• Mol File: 1404053-06-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N,N-diphenyl-4-[2-[4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)phenyl]ethenyl]-benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diphenyl-4-[2-[4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)phenyl]ethenyl]-benzenamine(1404053-06-0)
• EPA Substance Registry System: N,N-diphenyl-4-[2-[4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)phenyl]ethenyl]-benzenamine(1404053-06-0)

Safety Data

• Hazardous Substances Data: 1404053-06-0(Hazardous Substances Data)

Upstream product

• 219987-44-7 N-{4-[2-(4-bromophenyl)vinyl]phenyl}-diphenylamine 
• 73183-34-3 bis(pinacol)diborane 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 38257-52-2 4-(N,N-diphenylamino)iodobenzene 

Downstream Products

• 1404053-08-2 4,7-bis{5-{4-{2-[4-(N,N-diphenylamino)phenyl]-1-ethenyl}phenyl}-2-thienyl}-5,6,-bis(otcyloxy)-2,1,3-benzothiadiazole 
• 1607819-44-2 C₈₂H₇₈N₄O₂S₂ 

Relevant articles and documents

Linkage effects of linear D-π-A-π-D type diketopyrrolopyrrole- triphenylamine based solution-processable organic small molecule photovoltaic materials

Four novel D-π-A-π-D-type small molecules (SMs) were synthesized and their π-linkage effects were investigated. Among them, SM2 with vinylene as the π-linkage exhibited better molecular coplanarity, reaching a relatively higher power conversion efficiency (PCE) of 3.76%. SM3 and SM4 with acetylene and acrylonitrile as π-linkages exhibited relatively higher open-circuit voltages (VOC) of 0.93 V and 0.90 V, respectively, owing to their deep-lying HOMO levels. These results gave an important guide for developing new materials in solution-processed small molecule solar cells.