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Structure of 1383682-59-4
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tert-Butyl 4-(4-amino-3-methylphenyl)piperidine-1-carboxylate features a piperidine core functionalized with a para-amino-meta-methyl aniline moiety, delivering enhanced solubility and stability under standard conditions. The tert-butyl ester group enables straightforward deprotection in acidic environments, facilitating integration into diverse synthetic sequences. This scaffold serves as a key intermediate for bioactive compound development.
tert-Butyl 4-(4-amino-3-methylphenyl)piperidine-1-carboxylate serves as a versatile building block for the synthesis of biologically active compounds, enabling efficient access to substituted piperidine scaffolds. The protected amine and aromatic functionality offer orthogonal reactivity, facilitating downstream transformations such as Suzuki-Miyaura coupling, reductive amination, or amide formation. Bench-stable and readily purified by standard chromatography, it functions as a key intermediate in medicinal chemistry campaigns targeting CNS modulators and kinase inhibitors.
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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: