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Structure of 1381959-73-4
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This bench-stable, moisture-tolerant piperazine derivative features a tert-butyl-protected amine and a hydrochloride salt form, enabling straightforward incorporation into synthetic sequences. The sterically hindered backbone resists undesired side reactions, while the carboxylate moiety facilitates efficient deprotection under standard conditions.
(S)-tert-Butyl 2-(tert-butyl)piperazine-1-carboxylate hydrochloride serves as a chiral piperazine building block with enhanced stability and ease of handling. Its tert-butyl protecting groups offer robustness under standard synthetic conditions, enabling selective deprotection and functionalization. The molecule facilitates efficient access to pharmaceutically relevant scaffolds through amine coupling, reductive amination, and metal-catalyzed transformations, making it a practical choice for medicinal chemistry campaigns requiring stereocontrol and scalable synthesis.
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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: