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Structure of 113778-69-1
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N-Methoxy-N-methylisobutyramide features a sterically hindered amide core that enhances hydrolytic stability while maintaining reactivity in peptide coupling. The methoxy and methyl groups confer favorable solubility and low nucleophilicity, enabling efficient incorporation into complex molecular architectures under mild conditions.
N-Methoxy-N-methylisobutyramide serves as a robust amide surrogate in peptide coupling and acylation reactions, offering improved reactivity and reduced racemization compared to traditional amides. Its sterically hindered isobutyryl backbone enhances stability and facilitates clean deprotection, while the methoxy group enables efficient activation under mild conditions. This compound functions effectively as a building block for diverse heterocyclic scaffolds and synthetic intermediates in medicinal chemistry workflows.
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Lot numbers can be found on the outside label of a product: