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Structure of 34271-27-7
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(R)-2-Acetamidobutanoic acid is a chiral building block featuring a defined stereochemistry at the C2 position, enabling precise incorporation into peptide mimetics and bioactive molecule scaffolds. The acetamido group provides a polar, hydrogen-bonding handle, while the carboxylic acid offers versatility in derivatization. This compound exhibits bench-stable handling characteristics and compatibility with standard synthetic protocols in medicinal chemistry workflows.
(R)-2-Acetamidobutanoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in peptide-based drug discovery. Its well-defined stereochemistry and stability under standard reaction conditions enable reliable incorporation into complex scaffolds. The molecule functions effectively in amide bond formation and facilitates derivatization via its carboxylic acid and acetamide groups, offering versatile access to functionalized intermediates used in medicinal chemistry and process 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-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: