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Structure of 534595-51-2
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1-Boc-4-(isopropylamino)piperidine features a protected piperidine core with a sterically hindered isopropylamino substituent, enabling stable incorporation into complex molecular architectures. This bench-stable derivative facilitates efficient synthesis of bioactive amines and serves as a key intermediate in medicinal chemistry campaigns requiring controlled nitrogen functionality.
1-Boc-4-(isopropylamino)piperidine serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds common in bioactive molecules. The Boc group provides stability and facilitates straightforward deprotection under mild acidic conditions. Its isopropylamino substituent offers favorable steric and electronic properties for target-directed synthesis, while the piperidine core supports diverse functionalization and coupling reactions in standard reductive amination and amide formation 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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: