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Merck
CN

723622

9H-Carbazole-9-(4-phenyl) boronic acid pinacol ester

95%

Synonym(s):

9-(4-(4,4,5,5-Tetramethy-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole

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About This Item

Empirical Formula (Hill Notation):
C24H24BNO2
Molecular Weight:
369.26
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
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Product Name

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.

Storage Class

11 - Combustible Solids

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)
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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