1357150-79-8

Basic information

• Product Name: 12,12-dimethyl-10-phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10,12-di hydro-10-azaindeno[2,1-b]fluorene
• Synonyms: 12,12-dimethyl-10-phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10,12-di hydro-10-azaindeno[2,1-b]fluorene
• CAS NO: 1357150-79-8
• Molecular Weight: 485.434
• Mol File: 1357150-79-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 12,12-dimethyl-10-phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10,12-di hydro-10-azaindeno[2,1-b]fluorene(CAS DataBase Reference)
• NIST Chemistry Reference: 12,12-dimethyl-10-phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10,12-di hydro-10-azaindeno[2,1-b]fluorene(1357150-79-8)
• EPA Substance Registry System: 12,12-dimethyl-10-phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10,12-di hydro-10-azaindeno[2,1-b]fluorene(1357150-79-8)

Safety Data

• Hazardous Substances Data: 1357150-79-8(Hazardous Substances Data)

Upstream product

• 854952-58-2 N-phenyl-9H-carbazol-3-boronic acid 
• 583-55-1 1-Bromo-2-iodobenzene 
• 1190100-35-6 3-(2-bromophenyl)-9-phenyl-9H-carbazole 
• 591-50-4 iodobenzene 
• 1257220-47-5 12,12-dimethyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene 
• 1257220-43-1 12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole 
• 1357150-72-1 N-(2-bromophenyl)-9,9-dimethyl-9H-fluoren-2-amine 
• 1257220-44-2 7-bromo-12,12-dimethyl-10-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene 
• 73183-34-3 bis(pinacol)diborane 

Relevant articles and documents

New organic electroluminescent compound and organic electroluminescent device comprising the same

The present invention relates to a novel organic light emitting compound and an organic light emitting device comprising the same. When employing a compound according to the present invention as a phosphorescent host material in a light emitting layer, it

ORGANIC COMPOUNDS AND LITHT EMITTING DIODE AND ORGANIC LIGHT EMITTIG DIODE DISPLAY DEVICE USING THE COMPOUNDS

The present invention relates to a carbazole moiety with an indolo condensation structure, an organic compound in which a hetero condensation ring having a conjugated structure is connected to an indolo carbazole moiety and, as necessary, a different hetero ring is connected to a hetero condensation ring moiety; and to a light emitting diode and an organic light emitting diode using the organic compound. The organic compound of the present invention has excellent thermal stability and color purity. Also, since the organic compound has excellent hole transporting characteristics and/or electron transporting characteristics, a driving voltage rise which may be caused by a delay of charging electrons in a light emitting diode can be prevented. Also, when the organic compound of the present invention is applied, electrons can be charged in balance in an organic material layer constituting the light emitting diode. Light emitting efficiency and a life span of an element can be improved, because light emitting can be induced in not only an interfacial area with an adjacent layer but also all areas of the organic material layer. Since a relatively broad band gap is contained in the organic compound of the present invention, the organic compound can be utilized as a host of the organic layer in the light emitting diode.(110) First electrode(120) Second electrodeCOPYRIGHT KIPO 2018

Organic compound and application thereof as well as organic electroluminescent device

The invention relates to the field of organic electroluminescent devices, and discloses an organic compound and application thereof as well as an organic electroluminescent device. The component is ofa structure as shown in a formula (1): A represents a diphenyl silyl group; B represents a gene shown in the formula (2), wherein B is bonded to A or L2 through an a ring; X1 represents C or N, and X1 has at least one group selected from the groups consisting of an alkyl group of C1-6 and an aryl group of C6-30 as a substituent to saturate X1; and any two adjacent groups of R11, R12, R13 and R14in a b ring form one group, and any one of the groups is cyclized to form the structure as shown in the formula (3). The organic electroluminescent device formed by the organic compound provided by the invention has the advantages of low driving voltage, long service life, high current efficiency and high brightness.