3-(4-Bromophenyl)-9-phenyl-9H-carbazole

Basic Information

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CAS Number

1028647-93-9

Molecular Formula

C24H16BrN

Molecular Weight

398.3 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Agricultural Chemicals Pesticides Herbicides

Basic Physical Properties

Melting Point

136.0 to 140.0 deg-C

Boiling Point

560.5℃ at 760 mmHg

SMILES

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c1ccc(cc1)n2c3ccccc3c4c2ccc(c4)c5ccc(cc5)Br

InChI

InChI=1S/C24H16BrN/c25-19-13-10-17(11-14-19)18-12-15-24-22(16-18)21-8-4-5-9-23(21)26(24)20-6-2-1-3-7-20/h1-16H

InChIKey

JEYLGFCAZBGCMC-UHFFFAOYSA-N

LogP

7.213200000000005

Topological Polar Surface Area

4.93 Å²

Hydrogen Bond Donor/Acceptor

0 / 1

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

3-(4-Bromophenyl)-9-phenyl-9H-carbazole
3-(4-broMophenyl)-9-phenyl Carbazole
N-phenyl-3-(4-broMophenyl)carbazole
3-(4-bromophenyl)-N-phenylcarbazole
3-(4-Bromo-phenyl)-9-phenyl-9H-carbazole
BrPPC
3-(4-broMophenyl)-9-phenyl Carbazole
3-(4-broMophenyl)-N-phenyl-9H-Carbazole
9H-Carbazole, 3-(4-bromophenyl)-9-phenyl-
3-(4-broMophenyl)-9-phenyl-9H-carbazole 003
3-(4-broMophenyl)-9-phenyl-9H-carbazole (BPPC)
3-(4-BroMophenyl)-9-phenyl-9H-carbazole,3-93-(4-broMophenyl)-N-phenylcarbazole

MDL Number

MFCD14582939

Customs Code

2933990090

FAQ

What are the physical and chemical properties of 3-(4-Bromophenyl)-9-phenyl-9H-carbazole (CAS: 1028647-93-9)?

3-(4-Bromophenyl)-9-phenyl-9H-carbazole is a solid compound with a crystalline form. It has a molecular weight of approximately 409.22 g/mol. This compound is poorly soluble in water but soluble in organic solvents like dichloromethane and chloroform. It shows low reactivity under normal conditions but can undergo photodimerization, making it suitable for applications requiring stability and light sensitivity.

How is 3-(4-Bromophenyl)-9-phenyl-9H-carbazole (CAS: 1028647-93-9) typically synthesized?

3-(4-Bromophenyl)-9-phenyl-9H-carbazole can be synthesized through the Friedel-Crafts alkylation of carbazole with 4-bromophenylacetylene. The reaction is typically catalyzed by a Lewis acid such as aluminum trichloride. The yield of the product can be high with proper reaction conditions and catalyst selection, ensuring high purity and selectivity.

What industries use 3-(4-Bromophenyl)-9-phenyl-9H-carbazole (CAS: 1028647-93-9)?

3-(4-Bromophenyl)-9-phenyl-9H-carbazole is used in the pharmaceutical industry for the development of photodynamic therapies and as a light-sensitive material. It is also utilized in the semiconductor industry for its photoelectronic properties, in polymer-based materials for its fluorescence and conductivity, and in sensors for its light-responsive characteristics.

What precautions should be taken when handling 3-(4-Bromophenyl)-9-phenyl-9H-carbazole (CAS: 1028647-93-9)?

When handling 3-(4-Bromophenyl)-9-phenyl-9H-carbazole, it is important to wear appropriate personal protective equipment (PPE) such as gloves, safety goggles, and a laboratory coat. The compound should be handled in a well-ventilated area or a fume hood to avoid inhalation. In case of a spill, it should be cleaned up carefully using appropriate absorbent materials, and the area should be properly decontaminated. Always refer to the safety data sheet (SDS) for detailed handling instructions.