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Catalog Number:
19389
CAS Number:
1081-04-5
5-Bromo-1H-indazole-3-carboxylic acid ethyl ester
Purity:
≥ 95% (NMR)
Synonym(s):
Ethyl 5-bromo-1H-indazole-3-carboxylate
Documents
$72.31 /250MG
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Product Information

5-Bromo-1H-indazole-3-carboxylic acid ethyl ester is a versatile compound with significant applications in pharmaceutical research and development. This compound is recognized for its unique bromine substitution, which enhances its reactivity and makes it an essential building block in the synthesis of various bioactive molecules. Researchers utilize this compound in the development of novel therapeutic agents, particularly in the fields of oncology and neurology, where indazole derivatives have shown promising results in preclinical studies. Its ability to act as a scaffold for further chemical modifications allows for the exploration of diverse pharmacological profiles, making it a valuable asset in drug discovery.

In addition to its pharmaceutical applications, 5-Bromo-1H-indazole-3-carboxylic acid ethyl ester is also employed in agrochemical formulations, where it contributes to the development of effective crop protection agents. Its stability and compatibility with various solvents further enhance its utility in laboratory settings. With its broad range of applications and potential for innovation, this compound stands out as a key ingredient for researchers and industry professionals seeking to advance their projects.

Synonyms
Ethyl 5-bromo-1H-indazole-3-carboxylate
CAS Number
1081-04-5
Purity
≥ 95% (NMR)
Molecular Formula
C10H9BrN2O2
Molecular Weight
269.1
MDL Number
MFCD05663980
PubChem ID
12689364
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Ethyl 5-bromo-1H-indazole-3-carboxylate
CAS Number
1081-04-5
Purity
≥ 95% (NMR)
Molecular Formula
C10H9BrN2O2
Molecular Weight
269.1
MDL Number
MFCD05663980
PubChem ID
12689364
Appearance
White crystalline powder
Conditions
Store at 0-8 °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-indazole-3-carboxylic acid ethyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer and anti-inflammatory drugs.
  • Biochemical Research: It is used in studies investigating enzyme inhibition and receptor activity, providing insights into cellular processes and potential therapeutic targets.
  • Material Science: The compound is explored for its properties in creating advanced materials, such as polymers and coatings, which can enhance durability and performance.
  • Agricultural Chemistry: It has applications in the formulation of agrochemicals, aiding in the development of effective pesticides and herbicides that improve crop yield.
  • Analytical Chemistry: The compound is employed in various analytical techniques, including chromatography, to help identify and quantify other chemical substances in complex mixtures.

Citations