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Structure of 1240586-48-4
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This bench-stable piperazine derivative features a tert-butyl ester group and two methyl substituents at the 2- and 5-positions, enabling straightforward functionalization. The stereochemistry at the 2R,5R centers provides defined spatial orientation for asymmetric synthesis applications. It integrates readily into medicinal chemistry campaigns requiring rigid, electron-rich heterocyclic scaffolds with enhanced solubility and metabolic stability.
(2R,5R)-tert-Butyl 2,5-dimethylpiperazine-1-carboxylate serves as a stereochemically defined piperazine scaffold for medicinal chemistry applications. Its tert-butyl ester group enables straightforward deprotection under mild acidic conditions, while the methyl substituents provide enhanced metabolic stability and steric control. The compound exhibits excellent bench stability and functional group tolerance, facilitating its use in diverse coupling reactions and heterocycle construction workflows.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: