N-Boc-2,6-diethyl-4-oxo-piperidine is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "N-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group attached to the nitrogen atom, commonly used in organic synthesis to protect amines. The compound features two ethyl groups at the 2 and 6 positions of the piperidine ring, contributing to its hydrophobic character and potentially influencing its solubility and reactivity. The presence of a keto group at the 4-position introduces a carbonyl functionality, which can participate in various chemical reactions, such as nucleophilic addition or condensation reactions. This compound is often utilized in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals, due to its structural features that may enhance biological activity. As with many organic compounds, its physical properties, such as melting point, boiling point, and solubility, would depend on the specific conditions and purity of the sample.

N-boc-2,6-diethyl-4-oxo-piperdine

1003843-30-8: N-Boc-2,6-diethyl-4-oxo-piperidine is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "N-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group attached to the nitrogen atom, commonly used in organic synthesis to protect amines. The compound features two ethyl groups at the 2 and 6 positions of the piperidine ring, contributing to its hydrophobic character and potentially influencing its solubility and reactivity. The presence of a keto group at the 4-position introduces a carbonyl functionality, which can participate in various chemical reactions, such as nucleophilic addition or condensation reactions. This compound is often utilized in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals, due to its structural features that may enhance biological activity. As with many organic compounds, its physical properties, such as melting point, boiling point, and solubility, would depend on the specific conditions and purity of the sample.

1-Piperidinecarboxylic acid, 2,6-diethyl-4-oxo-, 1,1-dimethylethyl ester, (2R,6S)-rel-

<p>(2R,6S)-rel-tert-Butyl 2,6-diethyl-4-oxopiperidine-1-carboxylate</p>

CAS 1003843-30-8

N-boc-2,6-diethyl-4-oxo-piperdine

1-Piperidinecarboxylic acid, 2,6-diethyl-4-oxo-, 1,1-dimethylethyl ester, (2R,6S)-rel-

Ref: IN-DA0001TU

(2R,6S)-rel-tert-Butyl 2,6-diethyl-4-oxopiperidine-1-carboxylate

Ref: 54-OR1042012

(2R,6S)-rel-tert-Butyl 2,6-diethyl-4-oxopiperidine-1-carboxylate

Ref: 10-F463438