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Catalog Number:
21167
CAS Number:
399-68-8
Acide 4-fluoro-1 H -indole-2-carboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide 4-fluoroindole-2-carboxylique
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$51.18 /250 mg
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Product Information

4-Fluoro-1H-indole-2-carboxylic acid is a versatile compound widely recognized for its applications in pharmaceutical research and organic synthesis. This compound features a fluorine atom that enhances its reactivity, making it a valuable intermediate in the synthesis of various bioactive molecules. Researchers often utilize 4-Fluoro-1H-indole-2-carboxylic acid in the development of novel pharmaceuticals, particularly in the design of indole-based compounds that exhibit significant biological activity, including anti-cancer and anti-inflammatory properties. Its unique structure allows for modifications that can lead to the discovery of new therapeutic agents, making it an essential tool for medicinal chemists.

In addition to its pharmaceutical applications, 4-Fluoro-1H-indole-2-carboxylic acid is also employed in the field of agrochemicals and materials science. Its ability to act as a building block in the synthesis of complex organic molecules opens up possibilities for creating innovative products in these industries. The compound's stability and reactivity make it an attractive option for researchers looking to explore new chemical pathways and develop advanced materials. With its broad range of applications, 4-Fluoro-1H-indole-2-carboxylic acid stands out as a key compound for professionals aiming to push the boundaries of chemical research and development.

Synonyms
Acide 4-fluoroindole-2-carboxylique
CAS Number
399-68-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C9H6FNO2
Molecular Weight
179.15
MDL Number
MFCD02664471
PubChem ID
4035579
Melting Point
220-224 ?C
Appearance
Poudre jaune pâle à beige
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide 4-fluoroindole-2-carboxylique
CAS Number
399-68-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C9H6FNO2
Molecular Weight
179.15
MDL Number
MFCD02664471
PubChem ID
4035579
Melting Point
220-224 ?C
Appearance
Poudre jaune pâle à beige
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

4-Fluoro-1H-indole-2-carboxylic acid 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, enhancing therapeutic efficacy.
  • Biochemical Research: It is used in studies to understand enzyme mechanisms and receptor interactions, providing insights that can lead to new drug discoveries.
  • Material Science: The compound is explored for its potential in creating novel materials, such as organic semiconductors, due to its unique electronic properties.
  • Agricultural Chemistry: It can be applied in the formulation of agrochemicals, contributing to the development of effective herbicides and fungicides, thus improving crop yield.
  • Analytical Chemistry: This chemical is utilized in analytical methods for detecting and quantifying indole derivatives, aiding in quality control and research applications.

Citations