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CAS 1081-05-6

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Ethyl 5-chloro-1H-indazole-3-carboxylate

Description:
Ethyl 5-chloro-1H-indazole-3-carboxylate is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a chlorine atom at the 5-position and an ethyl ester group at the 3-position contributes to its unique reactivity and properties. This compound is typically a white to off-white solid and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water. Ethyl 5-chloro-1H-indazole-3-carboxylate is often utilized in organic synthesis and medicinal chemistry, serving as an intermediate in the development of pharmaceuticals and agrochemicals. Its reactivity can be attributed to the presence of the carboxylate group, which can participate in various chemical reactions, including esterification and nucleophilic substitutions. Safety data should be consulted for handling, as with many chemical substances, it may pose health risks if not managed properly.
Formula:C10H9ClN2O2
InChI:InChI=1S/C10H9ClN2O2/c1-2-15-10(14)9-7-5-6(11)3-4-8(7)12-13-9/h3-5H,2H2,1H3,(H,12,13)
InChI key:InChIKey=RYZAFUIELFHCSW-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C=2C(NN1)=CC=C(Cl)C2
Synonyms:
  • 1H-Indazole-3-carboxylic acid, 5-chloro-, ethyl ester
  • Ethyl 5-Chloro-1H-Indazole-3-Carboxylate
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