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Structure of 76742-48-8
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Methyl 2,2-diethoxyacetimidate serves as a stable, bench-ready synthon for imine-based transformations. Featuring a protected imino group flanked by two ethoxy substituents, it enables reliable access to α-aminocarbonyl derivatives under mild conditions. The diethoxy acetal moiety enhances stability while maintaining reactivity in nucleophilic addition sequences.
Methyl 2,2-diethoxyacetimidate serves as a reliable enol ether equivalent for the synthesis of α,α-disubstituted amides and imines. Its bench-stable nature and compatibility with mild acid conditions enable efficient access to diverse heterocyclic scaffolds, including pyrrolidines and oxazolidinones. The diethoxy group enhances solubility and facilitates purification, while the imidate functionality reacts selectively with electrophiles under standard conditions, offering predictable outcomes in multi-step sequences.
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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: