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Structure of 180975-66-0
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tert-Butyl cis-2,6-dimethylpiperazine-1-carboxylate features a sterically hindered piperazine core with defined cis stereochemistry, enabling precise control in medicinal chemistry applications. The tert-butyl ester group provides enhanced stability and ease of deprotection under mild acidic conditions, facilitating downstream functionalization. This derivative delivers robust performance in peptide coupling and scaffold elaboration workflows.
tert-Butyl cis-2,6-dimethylpiperazine-1-carboxylate serves as a stable, bench-friendly building block for the construction of piperazine-based scaffolds in medicinal chemistry. Its protected amine functionality enables selective derivatization, while the cis-configured dimethyl substitution provides defined stereochemistry and enhanced conformational rigidity. The tert-butoxycarbonyl (Boc) group facilitates easy removal under mild acidic conditions, enabling straightforward access to functionalized piperazines used in API development.
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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: