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Catalog Number:
44525
CAS Number:
91348-45-7
3-Bromoindol-2-carboxilato de etilo
Purity:
≥ 95% (GC)
Synonym(s):
Éster etílico del ácido 3-bromoindol-2-carboxílico
Documents
$53.78 /1G
Tamaño
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Información del producto

Ethyl 3-Bromoindole-2-carboxylate is a versatile compound widely recognized for its applications in medicinal chemistry and organic synthesis. This compound features a bromo substituent that enhances its reactivity, making it an excellent building block for the synthesis of various bioactive molecules. Researchers utilize Ethyl 3-Bromoindole-2-carboxylate in the development of pharmaceuticals, particularly in the creation of indole derivatives that exhibit significant biological activity, including anticancer and antimicrobial properties. Its unique structure allows for modifications that can lead to novel compounds with tailored functionalities, making it a valuable asset in drug discovery and development.

In addition to its pharmaceutical applications, Ethyl 3-Bromoindole-2-carboxylate is also employed in the synthesis of complex organic molecules in the field of materials science. Its ability to participate in various chemical reactions, such as cross-coupling and cyclization, opens up opportunities for creating innovative materials with specific properties. This compound stands out due to its ease of use and the potential for high yields in synthetic processes, making it a preferred choice for researchers and industry professionals seeking efficient and effective solutions in their work.

Número CAS
91348-45-7
Fórmula molecular
C11H10BrNO2
Peso molecular
268.11
Número MDL
MFCD02071793
Punto de fusión
149 - 153 °C
Condiciones
Tienda en RT
Información general
Número CAS
91348-45-7
Fórmula molecular
C11H10BrNO2
Peso molecular
268.11
Número MDL
MFCD02071793
Punto de fusión
149 - 153 °C
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Ethyl 3-Bromoindole-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 drugs targeting neurological disorders.
  • Organic Synthesis: It is used in organic chemistry as a building block for creating complex molecules, allowing researchers to explore new chemical entities with potential therapeutic effects.
  • Biological Research: The compound is employed in studies investigating the biological activity of indole derivatives, which are known for their diverse roles in biological systems.
  • Agricultural Chemistry: Ethyl 3-Bromoindole-2-carboxylate is explored for its potential applications in developing agrochemicals, enhancing crop protection products.
  • Material Science: It is used in the synthesis of novel materials, including polymers and nanomaterials, which can have applications in electronics and coatings.

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