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Catalog Number:
21553
CAS Number:
2338-71-8
5-Fluoroindole-3-carboxaldéhyde
Purity:
≥ 99 % (HPLC)
Synonym(s):
5-Fluoro-1 H -indole-3-carbaldéhyde, 3-Formyl-5-fluoroindole
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Product Information

5-Fluoroindole-3-carboxaldehyde is a versatile compound that plays a significant role in various fields, particularly in pharmaceutical research and organic synthesis. This compound is recognized for its unique fluorine substitution, which enhances its reactivity and selectivity in chemical reactions. Researchers often utilize 5-Fluoroindole-3-carboxaldehyde as a key intermediate in the synthesis of biologically active molecules, including potential drug candidates. Its ability to participate in diverse reactions, such as nucleophilic additions and condensation reactions, makes it an invaluable tool for chemists aiming to develop new therapeutic agents.

In addition to its synthetic applications, 5-Fluoroindole-3-carboxaldehyde has garnered attention for its potential use in the development of fluorescent probes and materials due to its distinct electronic properties. This compound can be employed in the creation of novel indole derivatives, which are known for their wide-ranging biological activities, including anti-cancer and anti-inflammatory effects. With its unique properties and practical applications, 5-Fluoroindole-3-carboxaldehyde is an essential compound for researchers and industry professionals looking to innovate in the fields of medicinal chemistry and materials science.

Synonyms
5-Fluoro-1 H -indole-3-carbaldéhyde, 3-Formyl-5-fluoroindole
CAS Number
2338-71-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 9 H 6 FNO
Molecular Weight
163.15
MDL Number
MFCD00022719
PubChem ID
259089
Melting Point
159-166 ?C
Appearance
Poudre cristalline jaunâtre à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
5-Fluoro-1 H -indole-3-carbaldéhyde, 3-Formyl-5-fluoroindole
CAS Number
2338-71-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 9 H 6 FNO
Molecular Weight
163.15
MDL Number
MFCD00022719
PubChem ID
259089
Melting Point
159-166 ?C
Appearance
Poudre cristalline jaunâtre à blanc cassé
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-Fluoroindole-3-carboxaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer and anti-inflammatory drugs.
  • Biochemical Research: It is used in studies exploring the mechanisms of action of neurotransmitters, aiding researchers in understanding brain functions and potential treatments for neurological disorders.
  • Organic Synthesis: The compound is valuable in organic chemistry for creating complex molecules, offering a versatile building block for chemists working on innovative materials and compounds.
  • Fluorescent Probes: Its unique properties allow it to be used in the creation of fluorescent probes for bioimaging, enhancing the visualization of biological processes in live cells.
  • Agricultural Chemistry: This chemical is explored for its potential in developing agrochemicals, contributing to the formulation of safer and more effective pesticides and herbicides.

Citations