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Structure of 138227-63-1
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tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate features a piperidine core linked to a para-aminophenoxy moiety, enabling direct incorporation into bioactive scaffolds. The tert-butyl ester group provides stability and facilitates deprotection under mild acidic conditions. This compound serves as a key intermediate in the synthesis of kinase inhibitors and CNS-targeted therapeutics.
tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient construction of piperidine-based scaffolds through standard amine functionalization. The protected amine and phenoxy ether functionalities exhibit excellent bench stability and compatibility with diverse coupling reactions. Its ease of purification and predictable reactivity make it well-suited for medicinal chemistry campaigns requiring rapid access to analogues.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: