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Structure of 2349395-78-2
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This chiral piperazine derivative features a rigid, sterically defined scaffold with two methylated ring positions and a tert-butyl ester group. The (3R,6R) stereochemistry ensures high diastereoselectivity in downstream transformations. The molecule integrates readily into complex heterocyclic architectures, offering enhanced solubility and stability under standard bench conditions.
(3R,6R)-1-tert-Butyl 3-methyl 6-methylpiperazine-1,3-dicarboxylate serves as a stereochemically defined piperazine building block for medicinal chemistry and asymmetric synthesis. Its rigid, enantiopure framework facilitates controlled functionalization at both nitrogen centers, enabling access to complex heterocyclic scaffolds. The tert-butyl and methyl substituents provide steric protection and enhanced bench stability, while the dicarboxylate groups offer orthogonal handles for selective deprotection and conjugation in multi-step syntheses.
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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: