3,6-Dibromo-9-vinyl-9H-carbazole

Basic Information

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CAS Number

1214-16-0

Molecular Formula

C14H9Br2N

Molecular Weight

351.04 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Fine Chemicals Dyes and Pigments Organic Dyes

Agricultural Chemicals Pesticides Herbicides

Basic Physical Properties

SMILES

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C=CN1C2=C(C=C(C=C2)Br)C3=C1C=CC(=C3)Br

InChI

InChI=1S/C14H9Br2N/c1-2-17-13-5-3-9(15)7-11(13)12-8-10(16)4-6-14(12)17/h2-8H,1H2

InChIKey

ORMIJZCMQBMNFA-UHFFFAOYSA-N

LogP

5.420000000000003

Topological Polar Surface Area

4.93 Å²

Hydrogen Bond Donor/Acceptor

0 / 1

Complexity

281

Synonyms & References

English

D5426
SCHEMBL304192
DTXSID30348184
3,6-Dibromo-9-vinylcarbazole
AMY22864
ORMIJZCMQBMNFA-UHFFFAOYSA-N
1214-16-0
3,6-Dibromo-9-vinyl-9H-carbazole
3,6-Dibromo-9-vinyl-9H-carbazole #
F71978
MFCD00080466
3,6-dibromo-9-ethenylcarbazole
FT-0715256
3,6-Br N-vinylcarbazole
3,6-Dibrom-N-vinylcarbazol
3,6-dibromo-9-vinyl-carbazole
3,6-dibromo-N-vinylcarbazole
9H-Carbazole,3,6-dibromo-9-ethenyl

MDL Number

MFCD00080466

Customs Code

2933990090

FAQ

What are the physical and chemical properties of 3,6-Dibromo-9-vinyl-9H-carbazole (CAS: 1214-16-0)?

3,6-Dibromo-9-vinyl-9H-carbazole is a crystalline solid with a high molecular weight. It has a low solubility in water but is more soluble in organic solvents like chloroform and benzene. Chemically, it is less reactive towards nucleophiles due to the presence of bromine atoms and the vinyl group, making it suitable for specific synthetic applications. It decomposes above 300°C and shows typical carbazole spectral characteristics in UV-Vis and NMR spectroscopy.

How is 3,6-Dibromo-9-vinyl-9H-carbazole (CAS: 1214-16-0) typically synthesized?

3,6-Dibromo-9-vinyl-9H-carbazole is typically synthesized via the bromination of 9-vinylcarbazole followed by a coupling reaction with bromine. The reaction is conducted in anhydrous conditions, often using aluminium bromide as a catalyst. High selectivity and yield are achieved under these conditions, ensuring the formation of the desired dibrominated product.

What industries use 3,6-Dibromo-9-vinyl-9H-carbazole (CAS: 1214-16-0)?

3,6-Dibromo-9-vinyl-9H-carbazole is utilized in various industries, including pharmaceuticals for its electronic properties, polymers for its stability and color characteristics, sensors for its detection capabilities, and semiconductors for its use in organic light-emitting diodes (OLEDs). Its unique structure makes it valuable in materials science and advanced electronic applications.

What precautions should be taken when handling 3,6-Dibromo-9-vinyl-9H-carbazole (CAS: 1214-16-0)?

When handling 3,6-Dibromo-9-vinyl-9H-carbazole, it is crucial to wear appropriate Personal Protective Equipment (PPE) including gloves, goggles, and a lab coat. Store it in a fume hood to minimize exposure to vapors. In case of a spill, immediately notify the safety officer and follow the Material Safety Data Sheet (MSDS) guidelines for clean-up. Always ensure good ventilation and avoid contact with skin and eyes. Handling should be done in a well-ventilated area with appropriate spill kits and emergency showers available nearby.