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Catalog Number:
24181
CAS Number:
372089-59-3
6-bromo- 1H- indol-2-carboxilato de metilo
Purity:
≥ 98,5 % (ensayo)
Synonym(s):
Éster metílico del ácido 6-bromo-1 H -indol-2-carboxílico
Documents
$43.87 /1G
Tamaño
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Product Information

Methyl 6-bromo-1H-indole-2-carboxylate is a versatile chemical compound widely recognized for its applications in medicinal chemistry and organic synthesis. This compound, characterized by its unique indole structure, serves as a valuable intermediate in the development of various pharmaceuticals, particularly in the synthesis of bioactive molecules. Its bromine substituent enhances its reactivity, making it an ideal candidate for further functionalization, which is essential in drug discovery and development processes.

Researchers and industry professionals utilize Methyl 6-bromo-1H-indole-2-carboxylate for its potential in creating novel therapeutic agents, especially in the fields of oncology and neurology. Its ability to facilitate the introduction of diverse functional groups allows for the exploration of new chemical entities with improved efficacy and selectivity. The compound's favorable properties, including stability and ease of handling, further contribute to its appeal in laboratory settings, making it a preferred choice for synthetic chemists aiming to innovate in drug design and development.

Synonyms
Éster metílico del ácido 6-bromo-1 H -indol-2-carboxílico
CAS Number
372089-59-3
Purity
≥ 98,5 % (ensayo)
Molecular Formula
C10H8BrNO2
Molecular Weight
254.08
MDL Number
MFCD00590200
PubChem ID
754141
Melting Point
179 - 183 ?C
Appearance
Cristales amarillos
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
Éster metílico del ácido 6-bromo-1 H -indol-2-carboxílico
CAS Number
372089-59-3
Purity
≥ 98,5 % (ensayo)
Molecular Formula
C10H8BrNO2
Molecular Weight
254.08
MDL Number
MFCD00590200
PubChem ID
754141
Melting Point
179 - 183 ?C
Appearance
Cristales amarillos
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Methyl 6-bromo-1H-indole-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 new drugs targeting neurological disorders.
  • Organic Synthesis: It is frequently used in organic chemistry as a building block for creating complex molecules, allowing chemists to explore new chemical reactions and pathways.
  • Material Science: Researchers utilize this compound in the development of novel materials, such as polymers and coatings, that exhibit enhanced properties for industrial applications.
  • Biological Research: The compound is employed in studies investigating the biological activity of indole derivatives, contributing to the understanding of their mechanisms in various biological systems.
  • Agrochemical Formulations: Methyl 6-bromo-1H-indole-2-carboxylate is also explored in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides through its unique chemical properties.

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