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Structure of 1159598-21-6
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di-tert-Butyl (R)-2-(hydroxymethyl)piperazine-1,4-dicarboxylate features a chiral piperazine core with two sterically shielded tert-butyl esters and a pendant hydroxymethyl group. This configuration enables selective derivatization in asymmetric synthesis while maintaining stability under standard bench conditions.
di-tert-Butyl (R)-2-(hydroxymethyl)piperazine-1,4-dicarboxylate serves as a stereochemically defined, bench-stable building block for the synthesis of piperazine-based pharmaceutical intermediates. Its orthogonal protection pattern enables selective deprotection and functionalization, while the hydroxymethyl group facilitates downstream transformations such as oxidation, etherification, or coupling reactions. The compound functions effectively in multi-step syntheses requiring precise stereocontrol and robust handling under standard organic reaction conditions.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: