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Catalog Number:
21533
CAS Number:
4792-67-0
Ethyl 5-chloroindole-2-carboxylate
Purity:
≥ 98% (HPLC)
Synonym(s):
2-Carbethoxy-5-chloroindole, 5-Chloro-1H-indole-2-carboxylic acid ethyl ester
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Product Information

Ethyl 5-chloroindole-2-carboxylate is a versatile compound widely recognized for its applications in medicinal chemistry and organic synthesis. This compound features a chloro substituent on the indole ring, which enhances its reactivity and makes it an essential building block for the development of various pharmaceuticals. Researchers utilize Ethyl 5-chloroindole-2-carboxylate in the synthesis of indole derivatives, which are crucial in the creation of bioactive molecules, including potential anti-cancer agents and anti-inflammatory drugs. Its unique structure allows for modifications that can lead to compounds with improved efficacy and selectivity.

In addition to its pharmaceutical applications, Ethyl 5-chloroindole-2-carboxylate serves as an important intermediate in the production of agrochemicals and dyes, showcasing its versatility across different industries. The compound's favorable properties, such as stability and ease of handling, make it an attractive choice for researchers and manufacturers alike. With its potential to contribute to innovative solutions in drug discovery and development, Ethyl 5-chloroindole-2-carboxylate stands out as a valuable asset for professionals in the chemical and pharmaceutical sectors.

Synonyms
2-Carbethoxy-5-chloroindole, 5-Chloro-1H-indole-2-carboxylic acid ethyl ester
CAS Number
4792-67-0
Purity
≥ 98% (HPLC)
Molecular Formula
C11H10ClNO2
Molecular Weight
223.66
MDL Number
MFCD00005610
PubChem ID
78518
Melting Point
165-171 °C
Appearance
Yellowish powder
Conditions
Store at 0-8°C
General Information
Synonyms
2-Carbethoxy-5-chloroindole, 5-Chloro-1H-indole-2-carboxylic acid ethyl ester
CAS Number
4792-67-0
Purity
≥ 98% (HPLC)
Molecular Formula
C11H10ClNO2
Molecular Weight
223.66
MDL Number
MFCD00005610
PubChem ID
78518
Melting Point
165-171 °C
Appearance
Yellowish powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 5-chloroindole-2-carboxylate 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 agents. Its unique structure allows for modifications that enhance biological activity.
  • Biological Research: Researchers use it to study the mechanisms of action of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and antimicrobial properties.
  • Material Science: It is employed in the development of new materials, particularly in organic electronics and photonic devices, due to its electronic properties and stability.
  • Agricultural Chemistry: The compound is explored for its potential as a plant growth regulator, helping to improve crop yields and resistance to pests, thereby supporting sustainable agriculture.
  • Analytical Chemistry: Ethyl 5-chloroindole-2-carboxylate is used as a standard in analytical methods to quantify indole derivatives in various samples, ensuring accuracy in research and quality control in manufacturing.

Citations