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Structure of 1821799-48-7
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tert-Butyl (3R,4S)-4-amino-3-hydroxypiperidine-1-carboxylate delivers a chiral piperidine scaffold with defined stereochemistry at C3 and C4. This bench-stable derivative features a hydroxyl group flanked by an amino function, enabling direct incorporation into complex molecular architectures. The tert-butyl carbamate protects the amine during synthetic manipulations while allowing straightforward deprotection under mild acidic conditions.
tert-Butyl (3R,4S)-4-amino-3-hydroxypiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive piperidine derivatives. Its protected amine and hydroxyl groups enable orthogonal functionalization, while the (3R,4S) configuration supports predictable stereoselective transformations. The tert-butyl carbamate group provides bench stability and facilitates straightforward deprotection under mild acidic conditions, making it well-suited for iterative medicinal chemistry campaigns and API intermediate 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: