2-phenyl-9H-carbazole

Basic Information

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CAS Number

88590-00-5

Molecular Formula

C18H13N

Molecular Weight

243.31 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Basic Physical Properties

Density

1.208±0.06 g/cm3 (20 ºC 760 Torr),

Solubility

Insuluble (2.1E-4 g/L) (25 ºC),

SMILES

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C1=CC=C(C=C1)C2=CC3=C(C=C2)C4=CC=CC=C4N3

InChI

InChI=1S/C18H13N/c1-2-6-13(7-3-1)14-10-11-16-15-8-4-5-9-17(15)19-18(16)12-14/h1-12,19H

InChIKey

IMLDYQBWZHPGJA-UHFFFAOYSA-N

LogP

4.988100000000003

Topological Polar Surface Area

15.79 Å²

Hydrogen Bond Donor/Acceptor

1 / 1

Complexity

307

Safety Information

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Hazard Statement

H315 Causes skin irritation
Skin corrosion/irritation

H319 Causes serious eye irritation
Serious eye damage/eye irritation

Synonyms & References

English

2-phenyl-9H-Carbazole
2-phenylcarbazole
2-phenyl carbazole
9H-Carbazole, 2-phenyl-
IMLDYQBWZHPGJA-UHFFFAOYSA-N
AK402554
P2375
2-Phenyl-9H-carbazole (ACI)
Carbazole, 2-phenyl- (7CI)
2-Phenylcarbazole
AKOS027384128
DA-01548
F15297
88590-00-5
CS-0156408
MFCD26402145
DS-13453
SCHEMBL1900394
2-phenyl-9H-carbazole
CHEMBL1173702

MDL Number

MFCD26402145

FAQ

What are the physical and chemical properties of 2-phenyl-9H-carbazole (CAS: 88590-00-5)?

2-Phenyl-9H-carbazole is a yellow or orange crystalline solid with a molecular weight of approximately 210.22 g/mol. It has low solubility in water but good solubility in organic solvents such as dichloromethane and acetone. Chemically, it is stable under neutral and basic conditions but susceptible to oxidation and light. Its reactivity is moderate with some electrophilic aromatic substitution reactions possible under specific conditions.

How is 2-phenyl-9H-carbazole (CAS: 88590-00-5) typically synthesized?

2-Phenyl-9H-carbazole is typically synthesized via the Stille coupling reaction where phenylboronic acid and 9H-carbazole are coupled in the presence of a palladium catalyst and a base. The synthetic method provides good yield and selectivity for the target compound. Other methods include Suzuki coupling or direct condensation of phenylamine with 9H-carbazole under specific conditions.

What industries use 2-phenyl-9H-carbazole (CAS: 88590-00-5)?

2-Phenyl-9H-carbazole is used in a variety of industries. It is a key component in the synthesis of polymers for optical devices, as well as in the development of organic semiconductors for electronics. It also finds applications in the pharmaceutical industry for the synthesis of certain bioactive compounds, and in sensor technology for its unique optical properties.

What precautions should be taken when handling 2-phenyl-9H-carbazole (CAS: 88590-00-5)?

When handling 2-phenyl-9H-carbazole, use appropriate personal protective equipment (PPE) such as gloves and safety goggles. Work in a fume hood due to its potential for degradation under light. Spills should be cleaned up carefully using appropriate absorbents, and the area should be well ventilated. Consult the Safety Data Sheet (SDS) for specific handling and disposal instructions.