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Structure of 475105-35-2
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(S)-2-(Aminomethyl)-1-N-Boc-piperidine is a chiral building block featuring a protected amine and a pendant aminomethyl group, enabling direct incorporation into bioactive molecules. The Boc-protected nitrogen ensures stability during synthetic manipulations, while the (S)-configuration provides defined stereochemical control for asymmetric synthesis. This scaffold integrates readily into peptidomimetics and pharmaceutical intermediates under standard conditions.
(S)-2-(Aminomethyl)-1-N-Boc-piperidine serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient access to piperidine-containing scaffolds. The Boc-protected amine offers excellent stability and orthogonal deprotection compatibility, while the pendant primary amine facilitates diverse functionalizations. This compound functions effectively in standard coupling reactions, reductive amination protocols, and heterocycle construction, supporting scalable, bench-friendly workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H318
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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: