1-Piperidin-4-ylethanone, also known as 4-piperidone, is an organic compound characterized by its piperidine ring structure with a ketone functional group attached to the ethyl side chain. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. This compound is known for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It exhibits moderate polarity due to the presence of the ketone group, which influences its solubility in organic solvents. The compound has a distinct odor and is generally stable under standard conditions, although it may be sensitive to moisture and light. Its reactivity is primarily attributed to the carbonyl group, allowing it to participate in nucleophilic addition reactions. Safety precautions should be taken when handling this substance, as it may pose health risks if inhaled or ingested. Overall, 1-piperidin-4-ylethanone is a valuable compound in synthetic organic chemistry with diverse applications.

1-piperidin-4-ylethanone

30818-11-2: 1-(Piperidin-4-yl)ethanone, Ethanone, 1-(4-Piperidinyl)-

1-(Piperidin-4-yl)ethanone is a metabolite of the antibiotic, pyrazinamide. It is an antimycobacterial agent and has been shown to be effective against strains of tuberculosis, but not against other mycobacteria such as Mycobacterium avium complex. 1-(Piperidin-4-yl)ethanone has been shown to inhibit cellular growth by preventing the synthesis of DNA, RNA, and proteins. The mechanism of action for this drug is unclear, but may involve inhibition of thione reductase enzymes. The biosynthesis of 1-(piperidin-4-yl)ethanone has been studied in detail using caco-2 cells and chromatographic methods. This compound can be synthesized from oxadiazolone through the chloroformate pathway or from acetaldehyde through dehydration.

CAS 30818-11-2: 1-piperidin-4-ylethanone

1-(Piperidin-4-yl)ethanone

Ref: 3D-FP154829

Ethanone, 1-(4-piperidinyl)-

Ref: IN-DA0031DX

1-(Piperidin-4-yl)ethanone

Ref: 10-F760734