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Structure of 912940-89-7
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This chiral building block features a protected piperidine moiety integrated with a carboxylic acid side chain, enabling direct incorporation into peptide and peptidomimetic architectures. The (R)-stereochemistry at the C3 position ensures precise spatial orientation in synthetic sequences. The tert-butoxycarbonyl group provides stable protection under standard conditions, simplifying downstream deprotection and functionalization workflows.
(R)-2-(1-(tert-Butoxycarbonyl)piperidin-3-yl)acetic acid serves as a versatile chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry. The protected piperidine moiety enables efficient functionalization and orthogonal deprotection, while the acetic acid side chain facilitates conjugation or further derivatization. Bench-stable and readily purified by standard chromatographic methods, it functions reliably in peptide coupling, heterocycle formation, and scaffold elaboration 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-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: