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723622

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

Name: 9<I>H</I>-Carbazole-9-(4-phenyl) boronic acid pinacol ester
Brand: ALDRICH

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:

329764022

UNSPSC Code:

12352103

MDL number:

MFCD16294549

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Properties

Quality Level

100

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

Description

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).

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)

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)

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)

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Global Trade Item Number

SKU	GTIN
723622-1G	04061832861197
723622-5G	04061833501252