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Catalog Number:
21592
CAS Number:
16732-70-0
Éster etílico del ácido 5-bromoindol-2-carboxílico
Purity:
≥ 98% (ensayo)
Synonym(s):
Éster etílico del ácido 5-bromo-1 H -indol-2-carboxílico, 5-Bromo-2-carbetoxiindol, 5-Bromoindol-2-carboxilato de etilo
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Product Information

5-Bromoindole-2-carboxylic acid ethyl ester is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound, characterized by its bromine substitution on the indole ring, serves as a valuable intermediate in the development of various bioactive molecules. Its unique structure allows for the modification of the indole framework, making it an essential building block in the synthesis of indole-based pharmaceuticals and agrochemicals. Researchers have leveraged its properties to explore new therapeutic agents, particularly in the fields of oncology and neurology, where indole derivatives have shown promising biological activities.

In addition to its applications in drug discovery, 5-Bromoindole-2-carboxylic acid ethyl ester is also employed in the synthesis of fluorescent probes and materials for organic electronics. Its ability to undergo various chemical transformations, such as coupling reactions and functional group modifications, enhances its utility in synthetic chemistry. With its favorable reactivity and functionalization potential, this compound stands out as a key player in advancing research and development across multiple scientific disciplines.

Synonyms
Éster etílico del ácido 5-bromo-1 H -indol-2-carboxílico, 5-Bromo-2-carbetoxiindol, 5-Bromoindol-2-carboxilato de etilo
CAS Number
16732-70-0
Purity
≥ 98% (ensayo)
Molecular Formula
C11H10BrNO2
Molecular Weight
268.11
MDL Number
MFCD00022701
PubChem ID
259091
Appearance
Polvo de color marrón a marrón oscuro
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Éster etílico del ácido 5-bromo-1 H -indol-2-carboxílico, 5-Bromo-2-carbetoxiindol, 5-Bromoindol-2-carboxilato de etilo
CAS Number
16732-70-0
Purity
≥ 98% (ensayo)
Molecular Formula
C11H10BrNO2
Molecular Weight
268.11
MDL Number
MFCD00022701
PubChem ID
259091
Appearance
Polvo de color marrón a marrón oscuro
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Bromoindole-2-carboxylic acid ethyl ester is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a key intermediate in the synthesis of various indole derivatives, which are important in the development of pharmaceuticals.
  • Pharmaceutical Development: It is used in the creation of novel drugs, particularly those targeting neurological disorders, due to its ability to modify biological activity.
  • Material Science: The compound can be incorporated into polymers to enhance their properties, such as thermal stability and mechanical strength, making it valuable in manufacturing.
  • Biochemical Research: Researchers utilize it to study enzyme interactions and signaling pathways, contributing to a better understanding of cellular processes.
  • Agrochemicals: It is explored for its potential use in developing new agrochemical products, providing solutions for pest control and crop protection.

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