723622
9H-Carbazole-9-(4-phenyl) boronic acid pinacol ester
95%
别名:
9-(4-(4,4,5,5-Tetramethy-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole
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选择尺寸
关于此项目
经验公式（希尔记法）:
C24H24BNO2
分子量:
369.26
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
产品名称
9H-Carbazole-9-(4-phenyl) boronic acid pinacol ester, 95%
InChI
1S/C24H24BNO2/c1-23(2)24(3,4)28-25(27-23)17-13-15-18(16-14-17)26-21-11-7-5-9-19(21)20-10-6-8-12-22(20)26/h5-16H,1-4H3
SMILES string
CC1(C)OB(OC1(C)C)c2ccc(cc2)-n3c4ccccc4c5ccccc35
InChI key
AHDSYMVAUJZCOP-UHFFFAOYSA-N
assay
95%
form
solid
mp
165-173 °C
Quality Level
Application
9H-Carbazole-9-(4-phenyl) boronic acid pinacol can be used as a donor molecule in the formation of novel donor-π-acceptor dyes for electrochemical applications. It can also be used in the formation of organic light emitting diodes (OLEDs).
General description
9H-Carbazole-9-(4-phenyl) boronic acid pinacol ester is a compound that is majorly used as an intermediate in electronic devices. Its molecular structure includes benzene rings, boronic acid pinacol ester and carbazole rings.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Spectroscopic studies on 9H-carbazole-9-(4-phenyl) boronic acid pinacol ester by DFT method
Sas EB, et al.
Journal of Molecular Structure, 1118, 124-138 (2016)
New V-shaped 2, 4-di (hetero) arylpyrimidine push-pull systems: Synthesis, solvatochromism and sensitivity towards nitroaromatic compounds
Verbitskiy EV, et al.
Dyes and Pigments, 159(3), 35-44 (2018)
Synthesis, photophysical and redox properties of the D-pi-A type pyrimidine dyes bearing the 9-phenyl-9H-carbazole moiety
Verbitskiy EV, et al.
Journal of Fluorescence, 25(3), 763-775 (2015)
Theoretical and experimental study on spectra, electronic structure and photoelectric properties of three nature dyes used for solar cells
Ren P, et al.
Journal of Molecular Liquids, 247(3), 193-206 (2017)
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