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Catalog Number:
19088
CAS Number:
773873-77-1
Ester méthylique de l'acide 5-bromo-1 H -indole-3-carboxylique
Purity:
≥ 97 % (HPLC)
Synonym(s):
5-bromo-1 H -indole-3-carboxylate de méthyle
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$58.39 /250 mg
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Product Information

5-Bromo-1H-indole-3-carboxylic acid methyl ester is a versatile compound widely utilized in pharmaceutical and chemical research. This compound, also known as methyl 5-bromo-1H-indole-3-carboxylate, features a bromine atom that enhances its reactivity, making it an essential building block in the synthesis of various bioactive molecules. Its unique structure allows for applications in medicinal chemistry, particularly in the development of novel therapeutic agents targeting a range of diseases, including cancer and neurological disorders. Researchers appreciate its ability to facilitate complex organic reactions, thus streamlining the synthesis of intricate compounds.

In addition to its pharmaceutical applications, 5-Bromo-1H-indole-3-carboxylic acid methyl ester serves as a valuable intermediate in the production of dyes and agrochemicals. Its stability and reactivity make it suitable for various chemical transformations, enabling the creation of compounds with tailored properties for specific applications. This compound not only enhances research efficiency but also opens avenues for innovation in drug discovery and material science.

Synonyms
5-bromo-1 H -indole-3-carboxylate de méthyle
CAS Number
773873-77-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C10H8BrNO2
Molecular Weight
254.08
MDL Number
MFCD06203728
PubChem ID
285091
Appearance
Poudre jaune à brune
Conditions
Conserver à 0-8 °C
General Information
Synonyms
5-bromo-1 H -indole-3-carboxylate de méthyle
CAS Number
773873-77-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C10H8BrNO2
Molecular Weight
254.08
MDL Number
MFCD06203728
PubChem ID
285091
Appearance
Poudre jaune à brune
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Bromo-1H-indole-3-carboxylic acid methyl ester is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile building block in the synthesis of various indole derivatives, which are important in the development of pharmaceuticals.
  • Pharmaceutical Development: It is employed in the design of new drugs, particularly those targeting neurological disorders, due to its structural similarity to bioactive compounds.
  • Biological Research: Researchers use this compound to study its effects on cellular processes, providing insights into cancer biology and potential therapeutic pathways.
  • Material Science: It finds applications in creating functional materials, such as organic semiconductors, due to its unique electronic properties.
  • Analytical Chemistry: The compound is utilized as a standard in chromatographic techniques, aiding in the accurate analysis of complex mixtures in various samples.

Citations