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CAS 1363381-41-2

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Methyl 5-bromo-1-methyl-1H-indazole-3-carboxylate

Description:
Methyl 5-bromo-1-methyl-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 bromine atom at the 5-position and a methyl group at the 1-position contributes to its unique reactivity and potential applications in medicinal chemistry. The carboxylate functional group, derived from the carboxylic acid, indicates that this compound can participate in various chemical reactions, such as esterification and nucleophilic substitutions. Its methyl ester form suggests it may exhibit different solubility properties compared to its acid counterpart, influencing its biological activity and interactions. This compound may be of interest in the development of pharmaceuticals, particularly in the context of drug design targeting specific biological pathways. As with many brominated compounds, it may also exhibit interesting electronic properties due to the presence of the halogen. Overall, Methyl 5-bromo-1-methyl-1H-indazole-3-carboxylate is a versatile compound with potential applications in various fields of chemistry and biology.
Formula:C10H9BrN2O2
InChI:InChI=1S/C10H9BrN2O2/c1-13-8-4-3-6(11)5-7(8)9(12-13)10(14)15-2/h3-5H,1-2H3
InChI key:InChIKey=LUFFZUUZKALCOA-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1C=2C(N(C)N1)=CC=C(Br)C2
Synonyms:
  • 1H-Indazole-3-carboxylic acid, 5-bromo-1-methyl-, methyl ester
  • Methyl 5-bromo-1-methyl-1H-indazole-3-carboxylate
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