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

Catalog Number:
17500
CAS Number:
21139-31-1
Acide 5-chloro-3-phényl-1H-indole-2-carboxylique
Purity:
≥ 95 % (RMN)
Documents
$72.31 /250 mg
Taille
Request Bulk Quote
Product Information

5-Chloro-3-phenyl-1H-indole-2-carboxylic acid is a versatile compound recognized for its significant applications in pharmaceutical research and organic synthesis. This compound features a unique indole structure that makes it particularly valuable in the development of novel therapeutic agents. Its chlorinated phenyl group enhances its reactivity, allowing for various substitution reactions that are essential in the synthesis of complex organic molecules. Researchers have utilized this compound in the synthesis of potential anti-cancer and anti-inflammatory agents, showcasing its importance in medicinal chemistry.

In addition to its pharmaceutical applications, 5-Chloro-3-phenyl-1H-indole-2-carboxylic acid serves as a key intermediate in the production of dyes and agrochemicals, demonstrating its relevance across multiple industries. Its ability to participate in diverse chemical reactions makes it an attractive choice for researchers looking to innovate in drug development and material science. With its unique properties and broad applicability, this compound is an essential addition to any laboratory focused on advanced chemical research.

CAS Number
21139-31-1
Purity
≥ 95 % (RMN)
Molecular Formula
C15H10ClNO2
Molecular Weight
271.7
MDL Number
MFCD00425492
PubChem ID
2764152
Melting Point
228-232 ?C
Appearance
Poudre cristalline jaune
Conditions
Conserver à 0-8°C
General Information
CAS Number
21139-31-1
Purity
≥ 95 % (RMN)
Molecular Formula
C15H10ClNO2
Molecular Weight
271.7
MDL Number
MFCD00425492
PubChem ID
2764152
Melting Point
228-232 ?C
Appearance
Poudre cristalline jaune
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Chloro-3-phenyl-1H-indole-2-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its unique structure allows for modifications that enhance biological activity.
  • Biochemical Research: Researchers use it to study enzyme interactions and metabolic pathways, providing insights into cellular processes and potential therapeutic targets.
  • Material Science: It is employed in the creation of novel materials, including polymers and coatings, due to its ability to impart specific chemical properties, such as increased stability and resistance to degradation.
  • Organic Synthesis: This compound is a valuable building block in organic synthesis, facilitating the creation of complex molecules through various chemical reactions, which is essential for developing new compounds in laboratories.
  • Analytical Chemistry: It is used as a reference standard in analytical methods, helping to ensure the accuracy and reliability of testing procedures in quality control and research settings.

Citations