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Structure of 19889-37-3
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2-Ethyl-2-methylbutanoic acid features a sterically hindered α-carbon that enhances its resistance to decarboxylation and oxidation under standard conditions. This structural rigidity supports its use in controlled synthetic pathways, particularly where stability of the carboxylic acid moiety is critical.
2-Ethyl-2-methylbutanoic acid serves as a valuable chiral building block in synthetic organic chemistry, offering a sterically hindered aliphatic carboxylic acid functionality. Its branched alkyl structure enhances metabolic stability and provides a robust scaffold for peptide mimetics and bioactive molecule synthesis. The compound exhibits good bench stability and facilitates efficient coupling reactions with minimal racemization, enabling straightforward incorporation into complex architectures via standard amide bond formation protocols.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: