5-Fluoro-1H-indazole-3-carbaldehyde 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 aldehyde functional group at the 3-position is significant for its reactivity, allowing for various chemical transformations, including condensation reactions and nucleophilic attacks. This compound is typically used in organic synthesis and may serve as an intermediate in the development of pharmaceuticals or agrochemicals. Its properties, such as solubility, melting point, and stability, can vary depending on the solvent and conditions used. Additionally, the fluorine substitution can enhance lipophilicity and influence the compound's interaction with biological targets, making it of interest in medicinal chemistry. Overall, 5-fluoro-1H-indazole-3-carbaldehyde is a versatile compound with potential applications in various fields of research.

5-fluoro-1H-indazole-3-carbaldehyde

485841-48-3: 1H-indazole-3-carboxaldehyde, 5-fluoro-,  5-Fluoro-1H-indazole-3-carbaldehyde

5-FLUORO-1H-INDAZOLE-3-CARBALDEHYDE

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CAS 485841-48-3: 5-fluoro-1H-indazole-3-carbaldehyde

5-FLUORO-1H-INDAZOLE-3-CARBALDEHYDE

Ref: 10-F793343

5-fluoro-2h-indazole-3-carbaldehyde

Ref: 3D-FF104746

5-Fluoro-1H-indazole-3-carbaldehyde

Ref: IN-DA006WPF

5-Fluoro-1H-indazole-3-carbaldehyde

Ref: 10-F209361

5-Fluoro-1H-indazole-3-carbaldehyde

Ref: 54-PC903633