🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
21593
CAS Number:
16382-15-3
5-méthylindole-2-carboxylate d'éthyle
Purity:
≥ 98 % (HPLC)
Synonym(s):
2-carbéthoxy-5-méthylindole, Ester éthylique de l'acide 5-méthyl-1 H -indole-2-carboxylique
Documents
$36.65 /1G
Taille
Request Bulk Quote
Product Information

Ethyl 5-methylindole-2-carboxylate is a versatile compound recognized for its significant applications in the fields of organic synthesis and medicinal chemistry. This compound features a unique indole structure, which is pivotal in the development of various pharmaceuticals and agrochemicals. Its ability to serve as a building block in the synthesis of more complex molecules makes it an invaluable resource for researchers and industry professionals alike. Ethyl 5-methylindole-2-carboxylate is particularly noted for its role in the synthesis of bioactive compounds, including potential anti-cancer agents and other therapeutic drugs.

In addition to its pharmaceutical applications, this compound is also utilized in the development of specialty chemicals and fragrances, enhancing its appeal across multiple industries. Its favorable properties, such as stability and reactivity, allow for efficient incorporation into various chemical reactions, making it a preferred choice for chemists looking to streamline their synthesis processes. With its broad range of applications and potential for innovation, Ethyl 5-methylindole-2-carboxylate stands out as a key compound for advancing research and product development.

Synonyms
2-carbéthoxy-5-méthylindole, Ester éthylique de l'acide 5-méthyl-1 H -indole-2-carboxylique
CAS Number
16382-15-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 12 H 13 NO 2
Molecular Weight
203.24
MDL Number
MFCD00022703
PubChem ID
232919
Melting Point
160-164 °C
Appearance
Solide jaune clair à brun pâle
Conditions
Conserver à 0-8 °C
General Information
Synonyms
2-carbéthoxy-5-méthylindole, Ester éthylique de l'acide 5-méthyl-1 H -indole-2-carboxylique
CAS Number
16382-15-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 12 H 13 NO 2
Molecular Weight
203.24
MDL Number
MFCD00022703
PubChem ID
232919
Melting Point
160-164 °C
Appearance
Solide jaune clair à brun pâle
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl 5-methylindole-2-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides, which helps in improving crop yield and protection.
  • Flavor and Fragrance Industry: Ethyl 5-methylindole-2-carboxylate is employed in creating specific flavor profiles and fragrances, making it valuable in food and cosmetic products.
  • Research in Organic Synthesis: This compound is a key building block in organic synthesis, allowing researchers to create complex molecules efficiently, which is crucial in various chemical research projects.
  • Material Science: It finds applications in developing new materials, particularly in polymers, where it can enhance properties such as durability and resistance to environmental factors.

Citations