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Catalog Number:
20888
CAS Number:
37033-94-6
2-carbéthoxy-5-éthylindole
Purity:
≥ 99% (GC)
Synonym(s):
Ester éthylique de l'acide 5-éthylindole-2-carboxylique, 5-éthyl-1 H -indole-2-carboxylate d'éthyle
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Product Information

2-Carbethoxy-5-ethylindole is a versatile compound that has garnered attention in various fields, particularly in organic synthesis and medicinal chemistry. This indole derivative features a unique ethyl carbethoxy group, which enhances its reactivity and allows for a range of functionalization possibilities. Researchers have utilized 2-Carbethoxy-5-ethylindole in the development of novel pharmaceuticals, particularly in the synthesis of indole-based compounds that exhibit significant biological activity. Its structural properties make it an excellent candidate for applications in drug discovery, where it can serve as a building block for creating complex molecules with potential therapeutic effects.

In addition to its pharmaceutical applications, 2-Carbethoxy-5-ethylindole is also relevant in the field of agrochemicals, where it can be explored for its potential as a pesticide or herbicide. The compound's stability and reactivity make it suitable for various formulations, providing an edge over similar compounds in terms of efficacy and safety. With its promising applications and unique properties, 2-Carbethoxy-5-ethylindole stands out as a valuable resource for researchers and industry professionals looking to innovate in their respective fields.

Synonyms
Ester éthylique de l'acide 5-éthylindole-2-carboxylique, 5-éthyl-1 H -indole-2-carboxylate d'éthyle
CAS Number
37033-94-6
Purity
≥ 99% (GC)
Molecular Formula
C 13 H 15 NO 2
Molecular Weight
217.27
MDL Number
MFCD00022704
PubChem ID
37610
Melting Point
101-107 ?C
Appearance
Poudre cristalline blanc cassé à jaune
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester éthylique de l'acide 5-éthylindole-2-carboxylique, 5-éthyl-1 H -indole-2-carboxylate d'éthyle
CAS Number
37033-94-6
Purity
≥ 99% (GC)
Molecular Formula
C 13 H 15 NO 2
Molecular Weight
217.27
MDL Number
MFCD00022704
PubChem ID
37610
Melting Point
101-107 ?C
Appearance
Poudre cristalline blanc cassé à jaune
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

2-Carbethoxy-5-ethylindole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of new drugs targeting neurological disorders.
  • Organic Synthesis: It is used in organic chemistry for creating complex molecules, allowing researchers to explore new chemical reactions and pathways.
  • Material Science: The compound can be incorporated into polymers and materials, enhancing their properties for applications in coatings and adhesives.
  • Biological Research: It plays a role in studying indole derivatives, which are important in understanding biological processes and developing new therapeutic agents.
  • Agricultural Chemistry: This chemical is investigated for its potential use in agrochemicals, contributing to the development of safer and more effective pesticides.

Citations