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Catalog Number:
21544
CAS Number:
877-03-2
5-Bromoindole-3-carboxaldéhyde
Purity:
≥ 98 % (HPLC)
Synonym(s):
5-Bromo-1 H -indole-3-carbaldéhyde, 5-Bromo-3-formylindole, 5-Bromoindole-3-aldéhyde
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Product Information

5-Bromoindole-3-carboxaldehyde is a versatile chemical compound widely utilized in various fields, particularly in organic synthesis and medicinal chemistry. This compound, characterized by its bromine substitution and aldehyde functional group, serves as a crucial intermediate in the synthesis of biologically active molecules. Researchers often leverage its unique reactivity to develop novel pharmaceuticals, agrochemicals, and dyes. Its ability to participate in diverse chemical reactions, such as nucleophilic additions and condensation reactions, makes it an invaluable tool for chemists aiming to create complex structures efficiently.

In addition to its synthetic applications, 5-Bromoindole-3-carboxaldehyde has shown potential in the development of fluorescent probes and sensors, enhancing its relevance in analytical chemistry. Its distinct properties allow for the exploration of new pathways in drug discovery, particularly in targeting specific biological pathways. With its broad applicability and unique features, this compound stands out as a key player in advancing research and development across multiple scientific disciplines.

Synonyms
5-Bromo-1 H -indole-3-carbaldéhyde, 5-Bromo-3-formylindole, 5-Bromoindole-3-aldéhyde
CAS Number
877-03-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H6BrNO
Molecular Weight
224.06
MDL Number
MFCD00152016
PubChem ID
70137
Melting Point
199-205 ?C
Appearance
Poudre cristalline jaune
Conditions
Conserver à 0-8 °C
General Information
Synonyms
5-Bromo-1 H -indole-3-carbaldéhyde, 5-Bromo-3-formylindole, 5-Bromoindole-3-aldéhyde
CAS Number
877-03-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H6BrNO
Molecular Weight
224.06
MDL Number
MFCD00152016
PubChem ID
70137
Melting Point
199-205 ?C
Appearance
Poudre cristalline jaune
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-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 pharmaceutical agents, particularly those targeting neurological disorders.
  • Fluorescent Probes: It is used in the development of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Organic Electronics: The compound plays a role in the fabrication of organic semiconductors, which are essential for the development of flexible electronic devices.
  • Biochemical Research: It is employed in the study of enzyme interactions and metabolic pathways, providing insights into biochemical processes.
  • Material Science: 5-Bromoindole-3-carboxaldehyde is used in the creation of advanced materials, such as polymers and nanocomposites, enhancing their properties for various applications.

Citations