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Structure of 788799-69-9
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(S)-1,4-Bis(tert-butoxycarbonyl)piperazine-2-carboxylic acid features two robust tert-butyl carbamate protecting groups flanking a chiral piperazine core, enabling stable incorporation into complex peptide architectures. The carboxylic acid moiety provides a reactive handle for conjugation under standard coupling conditions. This configuration supports efficient synthesis of constrained peptidomimetics and cyclic scaffolds with enhanced metabolic stability.
(S)-1,4-Bis(tert-butoxycarbonyl)piperazine-2-carboxylic acid serves as a versatile chiral building block for the synthesis of piperazine-based heterocycles. The molecule enables efficient construction of medicinally relevant scaffolds through orthogonal deprotection strategies, with both Boc groups offering predictable cleavage under mild acidic conditions. Its stability under ambient storage and compatibility with standard coupling protocols facilitate straightforward incorporation into peptide-like architectures and macrocyclic compounds.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: