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Catalog Number:
18102
CAS Number:
210345-56-5
Éster metílico del ácido 5-bromo-1 H -indol-2-carboxílico
Purity:
≥ 95% (RMN)
Synonym(s):
5-bromo- 1H- indol-2-carboxilato de metilo
Documents
$93.14 /250 mg
Tamaño
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Product Information

5-Bromo-1H-indole-2-carboxylic acid methyl ester is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This compound, also known as methyl 5-bromoindole-2-carboxylate, features a bromine atom that enhances its reactivity, making it an excellent building block for the development of various pharmaceuticals and agrochemicals. Its unique structure allows for the introduction of diverse functional groups, facilitating the synthesis of complex molecules. Researchers often leverage this compound in the design of indole-based derivatives, which have shown promising biological activities, including anti-cancer and anti-inflammatory properties.

In addition to its applications in drug discovery, 5-Bromo-1H-indole-2-carboxylic acid methyl ester is also valuable in materials science, particularly in the development of organic semiconductors and dyes. Its ability to participate in cross-coupling reactions further expands its utility in creating novel materials with tailored properties. With its broad range of applications and the potential for innovative uses, this compound is an essential resource for researchers and industry professionals looking to advance their projects.

Synonyms
5-bromo- 1H- indol-2-carboxilato de metilo
CAS Number
210345-56-5
Purity
≥ 95% (RMN)
Molecular Formula
C10H8BrNO2
Molecular Weight
254.08
MDL Number
MFCD01854034
PubChem ID
914343
Appearance
Marrón sólido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-bromo- 1H- indol-2-carboxilato de metilo
CAS Number
210345-56-5
Purity
≥ 95% (RMN)
Molecular Formula
C10H8BrNO2
Molecular Weight
254.08
MDL Number
MFCD01854034
PubChem ID
914343
Appearance
Marrón sólido
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-Bromo-1H-indole-2-carboxylic acid methyl 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 and agrochemicals.
  • Drug Development: Its unique structure allows researchers to explore its potential as a lead compound in the creation of new therapeutic agents, particularly in oncology and neurology.
  • Biological Research: The compound is used in studies investigating the mechanisms of action of indole-based compounds, contributing to the understanding of their biological activities.
  • Material Science: It can be incorporated into polymer matrices to enhance material properties, making it useful in the development of advanced materials for electronics and coatings.
  • Fluorescent Probes: Researchers utilize this compound in the design of fluorescent probes for biological imaging, providing insights into cellular processes and disease mechanisms.

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