Methyl 3-bromo-1H-indazole-5-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 3-position and a carboxylate group at the 5-position contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The methyl ester functional group enhances its solubility in organic solvents, making it suitable for various chemical reactions. This compound may exhibit biological activity, which is often explored in drug discovery and development. Its molecular structure allows for potential interactions with biological targets, making it of interest in pharmacological studies. Additionally, the presence of halogen substituents like bromine can influence the compound's electronic properties and reactivity, potentially leading to unique chemical behavior. Overall, Methyl 3-bromo-1H-indazole-5-carboxylate is a versatile compound with significant implications in research and development within the fields of chemistry and biochemistry.

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

1086391-06-1: 1H-Indazole-5-carboxylic acid, 3-bromo-, methyl ester

CAS 1086391-06-1: Methyl 3-bromo-1H-indazole-5-carboxylate

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

Ref: 3D-LTB39106

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

Ref: 10-F788334

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

Ref: IN-DA0083E6

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

Ref: 54-OR471693