Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
44511
CAS Number:
98600-34-1
4-Bromoindole-3-carboxaldehyde
Purity:
≥ 96% (GC)
Synonym(s):
4-Bromo-3-formylindole
Documents
$77.32 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

4-Bromoindole-3-carboxaldehyde is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound, characterized by its bromine substituent and aldehyde functional group, serves as a crucial building block in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for the synthesis of indole derivatives, which are essential in the creation of biologically active compounds. Researchers have leveraged 4-Bromoindole-3-carboxaldehyde in the synthesis of novel anti-cancer agents and other therapeutic molecules, showcasing its potential in drug discovery and development.

In addition to its applications in pharmaceuticals, 4-Bromoindole-3-carboxaldehyde is also valuable in materials science, particularly in the development of organic light-emitting diodes (OLEDs) and other electronic materials. Its ability to participate in various chemical reactions, such as condensation and coupling reactions, makes it an attractive option for chemists looking to innovate in both research and industrial applications. With its broad range of uses and the potential for further exploration, 4-Bromoindole-3-carboxaldehyde stands out as a significant compound in contemporary chemical research.

Synonyms
4-Bromo-3-formylindole
CAS Number
98600-34-1
Purity
≥ 96% (GC)
Molecular Formula
C9H6BrNO
Molecular Weight
224.06
MDL Number
MFCD05864695
PubChem ID
2763178
Melting Point
178 - 180 °C
Appearance
White to yellow powder to crystal
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-Bromo-3-formylindole
CAS Number
98600-34-1
Purity
≥ 96% (GC)
Molecular Formula
C9H6BrNO
Molecular Weight
224.06
MDL Number
MFCD05864695
PubChem ID
2763178
Melting Point
178 - 180 °C
Appearance
White to yellow powder to crystal
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Bromoindole-3-carboxaldehyde is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents and neuroprotective drugs.
  • Organic Electronics: It is used in the fabrication of organic light-emitting diodes (OLEDs) and organic solar cells, enhancing the efficiency and stability of these devices.
  • Fluorescent Probes: Researchers employ it to create fluorescent probes for biological imaging, allowing for the visualization of cellular processes in real-time.
  • Material Science: The compound is explored in the development of advanced materials, such as polymers and coatings, due to its unique electronic properties.
  • Biochemical Research: It plays a role in studying enzyme interactions and metabolic pathways, providing insights into various biological processes.

Citations