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Structure of 502482-52-2
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This piperidine-based scaffold features a protected hydroxyl group and a pendant acetic acid, enabling direct conjugation in peptide synthesis. The tert-butoxycarbonyl moiety ensures stability during handling and purification, while the carboxylic acid facilitates efficient coupling reactions under standard conditions.
2-(1-(tert-Butoxycarbonyl)-4-hydroxypiperidin-4-yl)acetic acid serves as a versatile building block for the synthesis of bioactive piperidine derivatives. The protected hydroxypiperidine moiety enables selective functionalization, while the acetic acid handle facilitates conjugation or further derivatization. Its bench-stable Boc group and orthogonal reactivity support efficient peptide and heterocycle assembly in medicinal chemistry 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: