1-Boc-3-fluoropiperidine-3-methanol is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in organic synthesis, particularly in the protection of amines. The presence of a fluorine atom at the 3-position of the piperidine ring introduces unique electronic and steric properties, which can influence the compound's reactivity and interaction with biological targets. The methanol group at the 3-position further adds to the compound's functionality, potentially allowing for hydrogen bonding and solubility in polar solvents. This compound is of interest in medicinal chemistry and drug development due to its structural features that may contribute to biological activity. Its synthesis and manipulation in laboratory settings require careful handling, particularly due to the presence of the fluorine atom, which can affect the compound's stability and reactivity. Overall, 1-Boc-3-fluoropiperidine-3-methanol serves as a versatile intermediate in the synthesis of various pharmaceutical agents.

1-Boc-3-fluoropiperidine-3-Methanol

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CAS 1209781-11-2: 1-Boc-3-fluoropiperidine-3-Methanol

TERT-BUTYL 3-FLUORO-3-(HYDROXYMETHYL)PIPERIDINE-1-CARBOXYLATE

Ref: 10-F305347

tert-butyl 3-(aMinoMethyl)-3-fluoropiperidine-1-carboxylate

Ref: IN-DA0099TX

1-Boc-3-fluoro-3-(hydroxymethyl)piperidine

Ref: 3D-JYB78111