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Structure of 923565-99-5
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(R)-Benzyl 2-methylpiperazine-1-carboxylate features a chiral piperazine core with a benzyloxycarbonyl protecting group, enabling direct incorporation into peptide-like scaffolds. The stereochemistry at the piperazine ring enhances target selectivity in medicinal chemistry applications. This bench-stable derivative offers improved solubility and handling over racemic analogs, streamlining synthetic workflows in drug discovery.
(R)-Benzyl 2-methylpiperazine-1-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling the construction of piperazine-based scaffolds prevalent in pharmaceuticals. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient synthesis of bioactive molecules. The protected amine and ester functionalities allow for orthogonal transformations, supporting diverse derivatization strategies in target-oriented 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: