Ethyl 5-fluoro-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 fluorine atom at the 5-position of the indazole ring contributes to its unique reactivity and potential biological activity. The ethyl ester functional group at the carboxylate position enhances its solubility in organic solvents and may influence its pharmacokinetic properties. This compound is often utilized in medicinal chemistry and drug development due to its potential as a scaffold for synthesizing bioactive molecules. Its structural features may allow for interactions with various biological targets, making it of interest in the fields of pharmaceuticals and agrochemicals. Additionally, the compound's stability and reactivity can be influenced by the presence of the fluorine atom, which can affect its electronic properties and steric hindrance. Overall, ethyl 5-fluoro-1H-indazole-3-carboxylate is a versatile compound with significant implications in chemical research and development.

ETHYL 5-FLUORO-1H-INDAZOLE-3-CARBOXYLATE

1016-36-0: Ethyl 5-fluoro-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 fluorine atom at the 5-position of the indazole ring contributes to its unique reactivity and potential biological activity. The ethyl ester functional group at the carboxylate position enhances its solubility in organic solvents and may influence its pharmacokinetic properties. This compound is often utilized in medicinal chemistry and drug development due to its potential as a scaffold for synthesizing bioactive molecules. Its structural features may allow for interactions with various biological targets, making it of interest in the fields of pharmaceuticals and agrochemicals. Additionally, the compound's stability and reactivity can be influenced by the presence of the fluorine atom, which can affect its electronic properties and steric hindrance. Overall, ethyl 5-fluoro-1H-indazole-3-carboxylate is a versatile compound with significant implications in chemical research and development.

1H-Indazole-3-carboxylic acid, 5-fluoro-, ethyl ester

<p>Ethyl 5-fluoro-1H-indazole-3-carboxylate</p>

CAS 1016-36-0

ETHYL 5-FLUORO-1H-INDAZOLE-3-CARBOXYLATE

1H-Indazole-3-carboxylic acid, 5-fluoro-, ethyl ester

Ref: IN-DA0004Y8

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

Ref: 54-PC108028