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Structure of 73569-40-1
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2,2-Dimethoxyacetic acid offers a stable, moisture-tolerant platform for C–C bond formation in synthetic workflows. The geminal dimethoxy group enhances electrophilicity at the alpha-carbon, enabling efficient coupling reactions under mild conditions. This bench-stable derivative integrates readily into complex molecular architectures requiring controlled reactivity and high functional group tolerance.
2,2-Dimethoxyacetic acid serves as a stable, bench-ready synthon for the introduction of α-oxoester functionality. Its dimethyl acetal group enables selective hydrolysis to generate reactive ketene intermediates under mild acidic conditions, facilitating efficient α-acylation or cycloaddition reactions. The compound exhibits excellent functional group tolerance and is readily purified by recrystallization, making it a practical building block in the synthesis of heterocyclic scaffolds and carbonyl-containing natural product analogs.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H335
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Precautionary Statements : P260-P261-P264-P271-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: