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CAS 102735-85-3

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4-Chloro-1H-indazole-3-carboxaldehyde

Description:
4-Chloro-1H-indazole-3-carboxaldehyde 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 chloro substituent at the 4-position and a carboxaldehyde group at the 3-position contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. This compound is typically a solid at room temperature and is soluble in organic solvents, making it useful for various chemical reactions. Its functional groups allow for further derivatization, which can lead to the development of biologically active molecules. The compound may exhibit specific biological activities, although detailed studies would be necessary to elucidate its pharmacological properties. As with many chemical substances, proper handling and safety precautions should be observed due to potential toxicity or reactivity. Overall, 4-Chloro-1H-indazole-3-carboxaldehyde serves as an important building block in the synthesis of more complex organic compounds.
Formula:C8H5ClN2O
InChI:InChI=1S/C8H5ClN2O/c9-5-2-1-3-6-8(5)7(4-12)11-10-6/h1-4H,(H,10,11)
InChI key:InChIKey=INZGVVZFYFGKJE-UHFFFAOYSA-N
SMILES:C(=O)C=1C=2C(NN1)=CC=CC2Cl
Synonyms:
  • 4-Chloro-3-(1H)Indazole
  • 1H-Indazole-3-carboxaldehyde, 4-chloro-
  • 4-CHLOROINDAZOLE-3-CARBOXYALDEHYDE
  • 4-Chloro-1H-indazole-3-carboxaldehyde
  • 4-Chloro-1H-indazole-3-carbaldehyde
  • 4-chloroindazole-3-carboxaldehyde
  • 4-CHLORO-3-(1H)INDAZOLE CARBOXALDEHYDE
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