ChemAbout
© 2026 ChemAbout
Insights|Privacy Policy|Terms of Service|[email protected]
Home/Compounds/Electronic Chemical/3-bromo-N-(2-biphenylyl)carbazole
C24H16BrN
398.3 g/mol
Electronic Chemical

3-bromo-N-(2-biphenylyl)carbazole

CAS1609267-04-0
Category
Electronic Chemical
Compound Class
Heterocycle
Primary Use
OLED material intermediate

3-Bromo-N-(2-biphenylyl)carbazole is a brominated carbazole derivative used as an intermediate in the production of OLED materials. Its structure consists of a carbazole core substituted with a bromine atom and a biphenyl group, contributing to its role in electronic and optoelectronic applications.

OLED material intermediate

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

Sourcing or supplying this compound?

List your inventory or post a purchase request

CAS 1609267-04-0

List This Product
Sign in to publish supply information
Request This Product
Submit a request without registering

Related Compounds

ApplicationSame Use

3'-Bromospiro[fluorene-9,9'-xanthene]

CAS1621397-55-4

OLED material intermediate

ApplicationSame Use

2-Bromobenzo[b]naphtho[2,3-d]furan

CAS1627917-16-1

OLED material intermediate

ApplicationSame Use

2-([1,1'-Biphenyl]-3-yl)-4-chloro-6-phenyl-1,3,5-triazine

CAS1689576-03-1

OLED material intermediate

ApplicationSame Use

2-(9,9'-Spirobi[fluoren]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS1346007-05-3

OLED material intermediate

ReferenceSame Category

2,4-dichloro-6-(3,5-diphenylphenyl)-1,3,5-triazine

CAS1616232-09-7

OLED material intermediate

ReferenceSame Category

4-Bromo-4'-tert-butylbiphenyl

CAS162258-89-1

Electronics chemical intermediate

ReferenceSame Category

Copper(II) Bis(trifluoromethanesulfonyl)imide

CAS162715-14-2

Lithium-ion battery electrolyte additive

Identifiers
IUPAC Name

3-bromo-9-(2-phenylphenyl)carbazole

InChIKey

JDGDLKDQACLMQC-UHFFFAOYSA-N

SMILES

C1=CC=C(C=C1)C2=CC=CC=C2N3C4=C(C=C(C=C4)Br)C5=CC=CC=C53

Synonyms (5)

—