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Structure of 10328-92-4
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N-Methylisatoic anhydride delivers a reactive, bench-stable platform for amide bond formation in synthetic chemistry. Featuring a sterically accessible anhydride moiety paired with a methyl-substituted isatoic scaffold, it facilitates efficient coupling under mild conditions. This derivative enables direct incorporation into peptide and small-molecule architectures without requiring pre-activation.
N-Methylisatoic anhydride serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted isoindolinones and related heterocyclic scaffolds. Its reactive anhydride functionality facilitates nucleophilic acylation under mild conditions, offering high functional group tolerance and excellent bench stability. The molecule functions as a key intermediate in the synthesis of pharmaceutical candidates and advanced materials, particularly where ortho-acylation and cyclization sequences are required.
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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: