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Structure of 71260-16-7
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2-Methyl-1-(piperazin-1-yl)propan-1-one features a reactive ketone group flanked by a sterically hindered methyl substituent and a piperazine ring, enabling efficient conjugation in synthetic transformations. This bench-stable scaffold integrates readily into bioactive molecule design, offering enhanced solubility and metabolic stability in medicinal chemistry applications.
2-Methyl-1-(piperazin-1-yl)propan-1-one serves as a versatile synthetic building block for medicinal chemistry and heterocyclic synthesis. Its α-ketoamide functionality enables direct incorporation into peptidomimetics and bioactive scaffolds via nucleophilic addition or condensation reactions. The piperazine moiety provides enhanced solubility and hydrogen-bonding capacity, while the methyl-substituted ketone offers steric control and metabolic stability. This compound demonstrates bench stability, compatibility with standard purification methods, and broad functional group tolerance in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: