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CAS 10250-63-2

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ETHYL 1-METHYL-3-PHENYL-1H-PYRAZOLE-5-CARBOXYLATE

Description:
Ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate, with the CAS number 10250-63-2, is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a phenyl group and a methyl group on the pyrazole ring enhances its chemical properties, potentially influencing its biological activity and interactions. Ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its applications may span various fields, including pharmaceuticals, where it could serve as a precursor or intermediate in the synthesis of bioactive compounds. The compound's reactivity can be attributed to the carboxylate group, which may participate in various chemical reactions, including esterification and nucleophilic substitutions. Overall, this compound is of interest for its structural features and potential applications in organic synthesis and medicinal chemistry.
Formula:C13H14N2O2
InChI:InChI=1/C13H14N2O2/c1-3-17-13(16)12-9-11(14-15(12)2)10-7-5-4-6-8-10/h4-9H,3H2,1-2H3
InChI key:InChIKey=JDJQHVJXMXXKFO-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=CC(=NN1C)C2=CC=CC=C2
Synonyms:
  • 1H-Pyrazole-5-carboxylic acid, 1-methyl-3-phenyl-, ethyl ester
  • 2-Methyl-5-phenyl-2H-pyrazole-3-carboxylic acid ethyl ester
  • Ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate 97%
  • Pyrazole-5-carboxylic acid, 1-methyl-3-phenyl-, ethyl ester
  • Salor-Int L201367-1Ea
  • Ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate
  • 5-(Ethoxycarbonyl)-1-methyl-3-phenyl-1H-pyrazole, 1-[5-(Ethoxycarbonyl)-1-methyl-1H-pyrazol-3-yl]benzene
  • Ethyl 1-Methyl-3-phenylpyrazole-5-carboxylate
  • 1H-Pyrazole-5-carboxylic acid, 1
  • JR-13855, Ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate, 95%
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