1-BOC-3-METHYL-PIPERIDIN-4-ONE, with the CAS number 181269-69-2, 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 protective group commonly used in organic synthesis, particularly in peptide chemistry, to temporarily mask amines. The presence of the methyl group at the 3-position of the piperidine ring contributes to the compound's steric and electronic properties, influencing its reactivity and interactions. This compound is typically utilized in the synthesis of various pharmaceuticals and agrochemicals, owing to its potential as an intermediate in organic synthesis. Its physical properties, such as solubility and boiling point, can vary depending on the specific conditions and purity of the compound. As with many nitrogen-containing heterocycles, it may exhibit basicity and can participate in various chemical reactions, including nucleophilic substitutions and cyclizations. Safety data should be consulted for handling and storage, as with all chemical substances.

1-BOC-3-METHYL-PIPERIDIN-4-ONE

181269-69-2: N-Tert-Butoxycarbonyl-3-Methyl-4-Piperidone, tert-Butyl 3-methyl-4-oxopiperidine-1-carboxylate

tert-Butyl 3-methyl-4-oxopiperidine-1-carboxylate

(R,S)-tert-Butyl 3-methyl-4-oxopiperidine-1-carboxylate

Tert-butyl 3-methyl-4-oxopiperidine-1-carboxylate is an optically active tertiary amine that is used in organic synthesis. Tert-butyl 3-methyl-4-oxopiperidine-1-carboxylate can be synthesized through the reaction of tertiary amines with methyl chloroformate and sodium ethoxide in a high yield. The compound has an optical rotation of [α]D = +5.5° (c=0.3, methanol).

CAS 181269-69-2: 1-BOC-3-METHYL-PIPERIDIN-4-ONE

tert-Butyl 3-methyl-4-oxopiperidine-1-carboxylate

Ref: 54-OR318070

1-BOC-3-METHYL-PIPERIDIN-4-ONE

Ref: IN-DA0022RJ

(R,S)-tert-Butyl 3-methyl-4-oxopiperidine-1-carboxylate

Ref: 10-F047014

tert-Butyl 3-methyl-4-oxopiperidine-1-carboxylate

Ref: 3D-FB29714