CAS 55119-09-0

1,3,6,8-tetrabromo-9H-carbazole

Description:

1,3,6,8-Tetrabromo-9H-carbazole is a halogenated organic compound characterized by the presence of four bromine atoms attached to a carbazole structure. This compound features a fused bicyclic system consisting of a benzene ring and a pyrrole-like structure, which contributes to its unique electronic properties. The tetrabromination enhances its stability and alters its reactivity, making it useful in various applications, including organic electronics and as a potential flame retardant. It is typically a solid at room temperature and may exhibit distinct color properties due to the presence of bromine substituents. The compound is of interest in research for its potential applications in materials science, particularly in the development of organic semiconductors and photonic devices. However, due to the presence of bromine, it may also raise environmental and health concerns, necessitating careful handling and disposal. As with many halogenated compounds, it is important to consider its toxicity and environmental impact during use and synthesis.

Formula: C₁₂H₅Br₄N

InChI: InChI=1/C12H5Br4N/c13-5-1-7-8-2-6(14)4-10(16)12(8)17-11(7)9(15)3-5/h1-4,17H

SMILES: c1c(cc(c2c1c1cc(cc(c1[nH]2)Br)Br)Br)Br

Synonyms:

• 1,3,6,8-Tetrabromocarbazole
• 9H-carbazole, 1,3,6,8-tetrabromo-

1,3,6,8-Tetrabromocarbazole

CAS: 55119-09-0

Formula: C₁₂H₅Br₄N

Purity: >95.0%(GC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 482.80

Ref: 3B-T2932

1,3,6,8-TetrabroMocarbazole

CAS: 55119-09-0

Formula: C₁₂H₅Br₄N

Purity: 95%

Color and Shape: Solid

Molecular weight: 482.7908

Ref: IN-DA00DBLP

1,3,6,8-Tetrabromo-9H-carbazole

CAS: 55119-09-0

1,3,6,8-Tetrabromo-9H-carbazole

Purity: 97%

Molecular weight: 482.79g/mol

Ref: 54-OR90635

1,3,6,8-Tetrabromo-9H-carbazole

CAS: 55119-09-0

Purity: 97%

Molecular weight: 482.7950134277344

Ref: 10-F622698

1,3,6,8-Tetrabromocarbazole

CAS: 55119-09-0

1,3,6,8-Tetrabromocarbazole is a brominated aromatic hydrocarbon that absorbs light in the ultraviolet region of the electromagnetic spectrum. It has been detected in marine sediments and soils near sites where it was used as an additive for polymers or paints. In recent years, 1,3,6,8-tetrabromocarbazole has also been found in human serum samples collected from people living near these sites. The uptake of this compound by humans may be due to its ability to cross the skin barrier and its high lipophilicity. This compound is not volatile and has a low vapor pressure. It is soluble in water but insoluble in acetone or ethanol. 1,3,6,8-Tetrabromocarbazole can be easily synthesized by coupling two molecules of benzene with one molecule of tetrabromoethane using a cross-coupling reaction. The optical properties

Formula: C₁₂H₅Br₄N

Purity: Min. 95 Area-%

Molecular weight: 482.79 g/mol

Ref: 3D-FT28064

1,3,6,8-Tetrabromocarbazole

Controlled Product

CAS: 55119-09-0

Applications A 9H-carbazole derivatives as potential immunomodulating agents.
References Duran-Galvan, M., et al.: Tetrahedron, 66, 7707 (2010),

Formula: C₁₂H₅Br₄N

Color and Shape: Neat

Molecular weight: 482.79

Ref: TR-T291330