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Structure of 1033709-36-2
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(R)-1-(2-Methylpiperazin-1-yl)ethanone is a chiral ketone featuring a piperazine core with a methyl substituent and a stereogenic center at the ethanone linkage. This configuration imparts distinct reactivity in asymmetric synthesis, enabling selective incorporation into bioactive scaffolds. The molecule exhibits favorable solubility in organic solvents and stability under standard bench conditions, facilitating use in medicinal chemistry workflows.
(R)-1-(2-Methylpiperazin-1-yl)ethanone serves as a versatile chiral building block in medicinal chemistry, enabling the construction of bioactive heterocycles and pharmaceutical scaffolds. Its amide functionality offers robust stability and compatibility with standard synthetic transformations, while the piperazinone core provides favorable solubility and hydrogen-bonding capacity. The (R)-stereocenter enhances target selectivity in CNS-directed compounds, and the molecule exhibits excellent bench stability and ease of purification—ideal for high-throughput screening and lead optimization workflows.
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Lot numbers can be found on the outside label of a product: