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Structure of 1488342-80-8
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tert-Butyl 4-(4-amino-3-fluorophenyl)piperidine-1-carboxylate features a fluorinated aromatic ring paired with a piperidine scaffold, enabling integration into bioactive molecules. This bench-stable derivative delivers a key pharmacophore for medicinal chemistry applications, combining enhanced solubility and metabolic stability in synthetic workflows.
tert-Butyl 4-(4-amino-3-fluorophenyl)piperidine-1-carboxylate serves as a versatile building block for medicinal chemistry campaigns, enabling direct incorporation of a fluorinated aniline motif into piperidine-based scaffolds. The tert-butyl carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. It functions reliably in standard coupling reactions and supports diverse downstream modifications, including reductive amination and amide formation, making it ideal for rapid lead optimization 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: