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4-Bromoindole
[CAS# 52488-36-5]

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Identification
Classification Organic raw materials >> Heterocyclic compound
Name 4-Bromoindole
Synonyms 4-Bromo-1H-indole
Molecular Structure CAS # 52488-36-5, 4-Bromoindole, 4-Bromo-1H-indole
Molecular Formula C8H6BrN
Molecular Weight 196.05
CAS Registry Number 52488-36-5
EC Number 610-851-5
SMILES C1=CC2=C(C=CN2)C(=C1)Br
Properties
Density 1.563
Melting point 17 ºC
Boiling point 283-285 ºC
Refractive index 1.655
Flash point 110 ºC
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H332
Eye irritationEye Irrit.2AH319
SDS Available
up Discovory and Applicatios
4-Bromoindole, an aromatic organic compound with the formula C₈H₆BrN, is a derivative of indole, a bicyclic heterocyclic compound containing a fused benzene and pyrrole ring. The bromine substituent at the 4-position of the indole ring imparts distinctive chemical properties and applications to 4-bromoindole.

The discovery of 4-bromoindole can be traced back to studies on substituted indoles in the early 20th century. Indole itself was first isolated from the fume of coal tar by the German chemist Ferdinand C. R. A. N. Meyer in 1866. Subsequent research into indole derivatives, including those with bromine substitutions, revealed their significant chemical reactivity and utility. The bromination of indole, specifically at the 4-position, was achieved using brominating agents such as bromine or bromine compounds under controlled conditions.

4-Bromoindole has found various applications in organic synthesis and medicinal chemistry due to its reactivity and the role of the bromine substituent. In organic synthesis, it is used as an intermediate for the preparation of more complex molecules. The presence of the bromine atom allows for further transformations through cross-coupling reactions, such as Suzuki or Heck reactions, which are widely utilized in the synthesis of pharmaceuticals and advanced materials.

In medicinal chemistry, 4-bromoindole serves as a key building block for the development of biologically active compounds. Its derivatives have been investigated for potential therapeutic applications, including as anti-cancer, anti-inflammatory, and antimicrobial agents. The bromine atom enhances the molecule's ability to interact with biological targets, making 4-bromoindole valuable in drug design and development.

The compound is also employed in materials science. For instance, 4-bromoindole derivatives have been used to create organic semiconductors and dyes. Their electronic properties and stability make them suitable for applications in organic light-emitting diodes (OLEDs) and photovoltaic cells.

Overall, 4-bromoindole is a versatile compound with significant utility in organic synthesis, medicinal chemistry, and materials science. Its role as an intermediate in the synthesis of complex molecules and its applications in developing therapeutic agents and advanced materials highlight its importance in both research and industrial fields.
Market Analysis Reports
List of Reports Available for 4-Bromoindole
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