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CAS 957129-38-3

:

5-Ethyl-4-methyl-1H-pyrazole-3-carboxylic acid

Description:
5-Ethyl-4-methyl-1H-pyrazole-3-carboxylic acid is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features an ethyl group and a methyl group as substituents on the pyrazole ring, contributing to its unique chemical properties. The presence of a carboxylic acid functional group (-COOH) at the 3-position enhances its acidity and reactivity, making it a potential candidate for various chemical reactions, including esterification and amidation. The compound is likely to exhibit moderate solubility in polar solvents due to the carboxylic acid group, while its hydrophobic ethyl and methyl groups may influence its overall solubility profile. Additionally, the compound may possess biological activity, which could be of interest in pharmaceutical research. Its specific applications and reactivity would depend on further studies, including its interaction with other chemical species and its behavior under different environmental conditions.
Formula:C7H10N2O2
InChI:InChI=1S/C7H10N2O2/c1-3-5-4(2)6(7(10)11)9-8-5/h3H2,1-2H3,(H,8,9)(H,10,11)
InChI key:InChIKey=MFNJGDMJKJLUGC-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C(C)=C(CC)NN1
Synonyms:
  • 5-Ethyl-4-methyl-1H-pyrazole-3-carboxylic acid
  • 5-Ethyl-4-methyl-2H-pyrazole-3-carboxylic acid
  • 3-Ethyl-4-methyl-1H-pyrazole-5-carboxylic acid
  • 1H-Pyrazole-3-carboxylic acid, 5-ethyl-4-methyl-
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