723622
9H-Carbazole-9-(4-phenyl) boronic acid pinacol ester
95%
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All Photos(3)
Synonym(s):
9-(4-(4,4,5,5-Tetramethy-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole
Empirical Formula (Hill Notation):
C24H24BNO2
Molecular Weight:
369.26
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
Assay
95%
form
solid
mp
165-173 °C
SMILES string
CC1(C)OB(OC1(C)C)c2ccc(cc2)-n3c4ccccc4c5ccccc35
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
InChI key
AHDSYMVAUJZCOP-UHFFFAOYSA-N
Related Categories
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.
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).
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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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)
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)
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)
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