1-bromo-9H-carbazole

Basic Information

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CAS Number

16807-11-7

Molecular Formula

C12H8BrN

Molecular Weight

246.11 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

122.0 to 126.0 deg-C

Boiling Point

409.2±18.0°C at 760 mmHg

Solubility

Insuluble (2.3E-3 g/L) (25 ºC),

SMILES

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C1=CC=C2C(=C1)C3=C(N2)C(=CC=C3)Br

InChI

InChI=1S/C12H8BrN/c13-10-6-3-5-9-8-4-1-2-7-11(8)14-12(9)10/h1-7,14H

InChIKey

VCDOOGZTWDOHEB-UHFFFAOYSA-N

LogP

4.0836000000000015

Topological Polar Surface Area

15.79 Å²

Hydrogen Bond Donor/Acceptor

1 / 1

Complexity

218

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

1-bromo-9H-Carbazole
1-Bromocarbazole
1-Bromcarbazol
1-Bromo-8-tetrahydropyranyloxyoctane
8-bromo-1-tetrahydro-2H-pyran-2-yloxyoctane
8-Bromooctan-1-ol tetrahydropyranyl ether
bromo-carbazole
-broMo-9H-carbazole
9H-Carbazole, 1-broMo-
AK166976
bromocarbazole
9H-Carbazole,1-bromo-
9H-arbazole, 1-romo-
VCDOOGZTWDOHEB-UHFFFAOYSA-N
BCP09057
FCH1375658
AMY19391
SY038343
CHEMBL5085077
SB66623
MFCD18450164
1-bromo-9H-carbazole
1-bromocarbazole
CS-W007242
DA-16674
A851662
16807-11-7
AS-10285
9H-Carbazole, 1-bromo-
F16028
SCHEMBL783567

MDL Number

MFCD18450164

Customs Code

2933990090

FAQ

What are the physical and chemical properties of 1-bromo-9H-carbazole (CAS: 16807-11-7)?

1-Bromo-9H-carbazole is a solid with a crystalline form. Its molecular weight is approximately 221.04 g/mol. This compound is poorly soluble in water but soluble in organic solvents like chloroform and ethanol. Chemically, it is reactive towards nucleophiles and can undergo substitution reactions. It is used in the synthesis of other compounds due to its aromatic nature and the presence of a bromine substituent.

How is 1-bromo-9H-carbazole (CAS: 16807-11-7) typically synthesized?

1-Bromo-9H-carbazole is typically synthesized by bromination of carbazole. The reaction is usually performed in the presence of a Lewis acid catalyst, such as AlCl3. The yield is generally high, and the product can be isolated by column chromatography. The reaction is selective and provides a high degree of purity.

What industries use 1-bromo-9H-carbazole (CAS: 16807-11-7)?

1-Bromo-9H-carbazole is used in the pharmaceutical industry for the synthesis of drugs that require specific aromatic structures. It is also used in the semiconductor industry for the development of organic semiconductors and in the polymer industry for the production of special polymers with unique properties. Additionally, it has applications in the sensor technology sector.

What precautions should be taken when handling 1-bromo-9H-carbazole (CAS: 16807-11-7)?

When handling 1-bromo-9H-carbazole, it is important to use appropriate personal protective equipment (PPE) such as gloves and safety glasses. The compound should be stored in a dry, well-ventilated area and should not be exposed to moisture or heat. Spills should be handled by professional hazmat personnel. Always refer to the Safety Data Sheet (SDS) for detailed safety information and emergency procedures.