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

Cat.No ACMA00016288

Basic Information Description Application Features And Benefits

Catalog Number	ACMA00016288
Synonyms	9-(4-(4,4,5,5-Tetramethy-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole
IUPAC Name	9-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbazole
Molecular Weight	369.26
Molecular Formula	C24H24BNO2
Canonical SMILES	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
Melting Point	165-173 °C
Storage	room temp
Assay	95%
MDL Number	MFCD16294549
NACRES	NA.23
Packaging	Packaging 1, 5 g in glass bottle
PubChem ID	329764022
Quality Level	100

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 s. It can also be used in the formation of organic light emitting diodes (OLEDs).

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