1-Boc-4-methoxypiperidine is a chemical compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group for amines, enhancing the compound's stability and reactivity in synthetic applications. The methoxy group (-OCH₃) at the 4-position of the piperidine ring contributes to the compound's overall polarity and can influence its solubility in various solvents. This compound is typically used in organic synthesis, particularly in the preparation of pharmaceuticals and other biologically active molecules. Its structure allows for various chemical modifications, making it a versatile intermediate in synthetic chemistry. Additionally, the presence of both the Boc and methoxy groups can affect the compound's reactivity, making it suitable for specific reactions such as nucleophilic substitutions or coupling reactions. Overall, 1-Boc-4-methoxypiperidine is valued for its functional groups that facilitate further chemical transformations in laboratory settings.

1-Boc-4-methoxypiperidine

188622-27-7: 1-Boc-4-methoxypiperidine is a chemical compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group for amines, enhancing the compound's stability and reactivity in synthetic applications. The methoxy group (-OCH₃) at the 4-position of the piperidine ring contributes to the compound's overall polarity and can influence its solubility in various solvents. This compound is typically used in organic synthesis, particularly in the preparation of pharmaceuticals and other biologically active molecules. Its structure allows for various chemical modifications, making it a versatile intermediate in synthetic chemistry. Additionally, the presence of both the Boc and methoxy groups can affect the compound's reactivity, making it suitable for specific reactions such as nucleophilic substitutions or coupling reactions. Overall, 1-Boc-4-methoxypiperidine is valued for its functional groups that facilitate further chemical transformations in laboratory settings.

CAS 188622-27-7

1-Boc-4-methoxypiperidine

1-BOC-4-methoxypiperidine

Ref: IN-DA002H2N

tert-Butyl 4-methoxypiperidine-1-carboxylate

Ref: 54-OR73255

TERT-BUTYL 4-METHOXYPIPERIDINE-1-CARBOXYLATE

Ref: 10-F390044