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Catalog Number:
21525
CAS Number:
776-41-0
Indole-3-Carboxylic acid ethyl ester
Purity:
≥ 99% (Assay)
Synonym(s):
3-Carbethoxyindole, Ethyl 1H-indole-3-carboxylate
Documents
$124.99 /1G
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Product Information

Indole-3-Carboxylic acid ethyl ester is a versatile compound widely recognized for its applications in organic synthesis and pharmaceutical research. This ethyl ester derivative of indole-3-carboxylic acid exhibits unique properties that make it a valuable building block in the development of various biologically active molecules. Its structure allows for easy modification, enabling researchers to explore a range of derivatives with potential therapeutic effects, particularly in the fields of oncology and neuropharmacology.

This compound is particularly useful in the synthesis of indole-based pharmaceuticals, which have been shown to possess anti-inflammatory, anti-cancer, and anti-microbial properties. Additionally, Indole-3-Carboxylic acid ethyl ester serves as an important intermediate in the production of agrochemicals and can be utilized in the development of novel materials. Its favorable reactivity and compatibility with various functional groups make it an essential tool for chemists looking to innovate in drug discovery and development.

Synonyms
3-Carbethoxyindole, Ethyl 1H-indole-3-carboxylate
CAS Number
776-41-0
Purity
≥ 99% (Assay)
Molecular Formula
C11H11NO2
Molecular Weight
189.21
MDL Number
MFCD00228454
PubChem ID
247965
Appearance
Off-white to pinkish powder
Conditions
Store at 0-8 °C
General Information
Synonyms
3-Carbethoxyindole, Ethyl 1H-indole-3-carboxylate
CAS Number
776-41-0
Purity
≥ 99% (Assay)
Molecular Formula
C11H11NO2
Molecular Weight
189.21
MDL Number
MFCD00228454
PubChem ID
247965
Appearance
Off-white to pinkish 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

Indole-3-Carboxylic acid ethyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with neurotransmitter systems.
  • Agricultural Applications: It is used in the formulation of plant growth regulators, enhancing crop yield and resilience by promoting root development and overall plant health.
  • Biochemical Research: Researchers employ this compound to study metabolic pathways in plants and animals, providing insights into cellular processes and potential therapeutic targets.
  • Material Science: Indole-3-Carboxylic acid ethyl ester is explored for its potential in creating novel materials, such as organic semiconductors, which can be used in electronic devices.
  • Cosmetic Formulations: The compound is also being investigated for its antioxidant properties, making it a candidate for inclusion in skincare products aimed at reducing oxidative stress on the skin.

Citations