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CAS 1346702-53-1

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2H-Indazole-4-carboxylic acid, 6-bromo-2-(1-methylethyl)-, methyl ester

Description:
2H-Indazole-4-carboxylic acid, 6-bromo-2-(1-methylethyl)-, methyl ester 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 carboxylic acid group and a methyl ester indicates that it has both acidic and ester functionalities, which can influence its reactivity and solubility. The bromine substituent at the 6-position introduces halogen characteristics, potentially enhancing the compound's reactivity in nucleophilic substitution reactions. The isopropyl group at the 2-position contributes to the compound's hydrophobic nature, which may affect its interaction with biological systems. This compound may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Its structural features suggest potential applications in drug development, particularly in targeting specific biological pathways. Overall, the combination of these functional groups and structural elements contributes to the compound's unique chemical properties and potential utility in various chemical and pharmaceutical applications.
Formula:C12H13BrN2O2
InChI:InChI=1S/C12H13BrN2O2/c1-7(2)15-6-10-9(12(16)17-3)4-8(13)5-11(10)14-15/h4-7H,1-3H3
InChI key:InChIKey=PIVQDVUHTABDHA-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1C=2C(=NN(C(C)C)C2)C=C(Br)C1
Synonyms:
  • Methyl 6-bromo-2-(1-methylethyl)-2H-indazole-4-carboxylate
  • 2H-Indazole-4-carboxylic acid, 6-bromo-2-(1-methylethyl)-, methyl ester
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