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Catalog Number:
17529
CAS Number:
43142-76-3
Éster etílico del ácido 5-cloro-3-formil-1 H -indol-2-carboxílico
Synonym(s):
5-cloro-3-formil- 1H- indol-2-carboxilato de etilo
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Product Information

5-Chloro-3-formyl-1H-indole-2-carboxylic acid ethyl ester is a versatile compound with significant potential in pharmaceutical and chemical research. This compound features a unique structure that allows for various modifications, making it an excellent candidate for the synthesis of biologically active molecules. Its ability to serve as an intermediate in the preparation of indole derivatives is particularly valuable, as indoles are known for their diverse pharmacological properties, including anti-inflammatory and anticancer activities. Researchers can leverage this compound in the development of novel therapeutic agents, enhancing their drug discovery efforts.

In addition to its synthetic utility, 5-Chloro-3-formyl-1H-indole-2-carboxylic acid ethyl ester exhibits favorable properties that facilitate its use in organic synthesis. Its reactivity and stability under various conditions make it suitable for applications in medicinal chemistry and material science. This compound can also be explored for its potential in agrochemical formulations, providing opportunities for innovation in crop protection. With its broad applicability and unique features, this compound is an essential addition to the toolkit of researchers and industry professionals alike.

Synonyms
5-cloro-3-formil- 1H- indol-2-carboxilato de etilo
CAS Number
43142-76-3
Molecular Formula
C12H10ClNO3
Molecular Weight
251.67
MDL Number
MFCD02257705
PubChem ID
4410568
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-cloro-3-formil- 1H- indol-2-carboxilato de etilo
CAS Number
43142-76-3
Molecular Formula
C12H10ClNO3
Molecular Weight
251.67
MDL Number
MFCD02257705
PubChem ID
4410568
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Synthesis of Pharmaceuticals: This compound serves as an intermediate in the synthesis of various pharmaceutical agents, particularly those targeting cancer and inflammatory diseases, enhancing drug discovery processes.
  • Biological Research: It is used in studies investigating the biological activity of indole derivatives, contributing to the development of new therapeutic compounds.
  • Material Science: The compound finds applications in creating novel materials with specific properties, such as organic light-emitting diodes (OLEDs), benefiting the electronics industry.
  • Agricultural Chemistry: It can be explored for developing agrochemicals that improve crop resistance to pests and diseases, supporting sustainable agricultural practices.
  • Analytical Chemistry: This compound is utilized in analytical methods for detecting and quantifying indole derivatives in various samples, aiding quality control in research and industry.

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