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Catalog Number:
17786
CAS Number:
192944-51-7
1H- indazole-5-carboxylate d'éthyle
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 1 H -indazole-5-carboxylique
Documents
$117.78 /250 mg
Taille
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Product Information

Ethyl 1H-Indazole-5-carboxylate is a versatile compound widely recognized for its applications in medicinal chemistry and organic synthesis. This compound features a unique indazole structure, which is known for its potential in developing novel pharmaceuticals. Researchers utilize Ethyl 1H-Indazole-5-carboxylate as a building block in the synthesis of various bioactive molecules, particularly in the creation of anti-inflammatory and anti-cancer agents. Its ability to undergo diverse chemical transformations makes it an essential intermediate in drug discovery and development processes.

In addition to its pharmaceutical relevance, Ethyl 1H-Indazole-5-carboxylate is also employed in agrochemical formulations, enhancing the efficacy of crop protection agents. Its favorable solubility and stability profiles contribute to its effectiveness in various formulations. With its broad range of applications, this compound stands out as a valuable asset for researchers and industry professionals seeking innovative solutions in drug development and agricultural chemistry.

Synonyms
Ester éthylique de l'acide 1 H -indazole-5-carboxylique
CAS Number
192944-51-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H10N2O2
Molecular Weight
190.2
MDL Number
MFCD03426220
PubChem ID
1501980
Appearance
Solide jaune
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester éthylique de l'acide 1 H -indazole-5-carboxylique
CAS Number
192944-51-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H10N2O2
Molecular Weight
190.2
MDL Number
MFCD03426220
PubChem ID
1501980
Appearance
Solide jaune
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

Ethyl 1H-Indazole-5-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 anti-cancer and anti-inflammatory agents.
  • Biological Research: It is used in studies investigating the mechanisms of action of indazole derivatives, contributing to the understanding of their biological properties and potential therapeutic effects.
  • Material Science: Ethyl 1H-Indazole-5-carboxylate is explored for its potential in creating novel materials, including polymers and coatings, due to its unique chemical structure.
  • Agricultural Chemistry: The compound is investigated for its applications in developing new agrochemicals, enhancing crop protection and yield through innovative formulations.
  • Analytical Chemistry: It is utilized as a standard in analytical methods to ensure the accuracy and reliability of testing procedures in various chemical analyses.

Citations