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Structure of 259180-79-5
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This tert-butyl (1-(2-aminoethyl)piperidin-4-yl)carbamate features a piperidine core functionalized with a primary amine and a robust tert-butyloxycarbonyl protecting group. The pendant aminoethyl side chain enables facile conjugation or further derivatization, while the carbamate moiety ensures stability during synthesis and storage. This compound serves as a key intermediate in the construction of bioactive molecules, particularly in medicinal chemistry campaigns targeting CNS therapeutics.
tert-Butyl (1-(2-aminoethyl)piperidin-4-yl)carbamate serves as a versatile bifunctional building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. The pendant primary amine facilitates conjugation and derivatization, while the tert-butoxycarbonyl (Boc) group provides orthogonal protection for nitrogen functionalization. Its stability under standard synthetic conditions and ease of deprotection make it ideal for multi-step synthesis and peptide-coupling workflows.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: