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Structure of 1691250-97-1
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tert-Butyl (2R,4R)-4-amino-2-methylpiperidine-1-carboxylate is a stereochemically defined piperidine derivative featuring a bench-stable tert-butyl carbamate protecting group. This configuration enables efficient incorporation into complex molecular architectures, particularly in the synthesis of bioactive heterocycles and peptidomimetics. The amino functionality supports direct derivatization, while the methyl substituent enhances steric control during cyclization steps.
tert-Butyl (2R,4R)-4-amino-2-methylpiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive piperidine derivatives. The protected amine and chiral methylpiperidine core enable direct incorporation into medicinal chemistry campaigns, facilitating efficient access to constrained scaffolds via standard coupling, alkylation, or reductive amination protocols. Bench-stable and compatible with diverse functional groups, it functions as a versatile intermediate in API development workflows requiring precise stereocontrol.
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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: