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Structure of 112106-16-8
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This chiral β-keto acid features a tert-butoxy carbonyl group flanking a stereogenic center, enabling selective functionalization in asymmetric synthesis. The pendant pentanoic acid chain provides a handle for derivatization, while the bench-stable, moisture-tolerant structure simplifies handling under standard conditions.
(R)-2-(2-(tert-Butoxy)-2-oxoethyl)pentanoic acid serves as a versatile chiral building block for synthesizing bioactive molecules, leveraging its pendant ketone and carboxylic acid functionalities. The tert-butoxycarbonyl group enables protection of the α-amino moiety in subsequent transformations, while the stereogenic center ensures enantioselective outcomes in peptide-like scaffold construction. Its bench-stable nature and compatibility with standard coupling and reduction protocols facilitate efficient access to complex intermediates 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: