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Structure of 343788-69-2
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1-Boc-4-Amino-4-methylpiperidine delivers a protected amine handle for late-stage functionalization in medicinal chemistry. The tert-butyl carbamate group ensures stability and ease of removal under mild acidic conditions. This piperidine derivative features a sterically hindered methyl substituent that modulates basicity and conformational flexibility, enhancing bioavailability in target-directed synthesis workflows.
1-Boc-4-Amino-4-methylpiperidine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted piperidine scaffolds. The Boc group provides excellent stability and orthogonal protection, facilitating straightforward deprotection under mild acidic conditions. Its tertiary amine functionality supports diverse functionalization, including reductive amination and coupling reactions, while the methyl substituent enhances metabolic stability and modulates lipophilicity in bioactive molecule design.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: