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Structure of 3469-00-9
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Methyl 2,2-diphenylacetate features a sterically hindered benzylic ester core flanked by two aryl groups, conferring enhanced stability under standard conditions. This bench-stable reagent integrates readily into synthetic sequences requiring robust ketone equivalents, enabling efficient access to diaryl-substituted carbonyl architectures through hydrolysis or reduction pathways.
Methyl 2,2-diphenylacetate serves as a stable, bench-ready synthon for the synthesis of diaryl-substituted carboxylic acid derivatives. Its α,α-diphenyl substitution imparts enhanced stability and facilitates efficient functionalization at the benzylic position. The ester group enables straightforward hydrolysis to the corresponding acid or conversion into amides and other carbonyl derivatives. This compound functions reliably in standard synthetic workflows involving nucleophilic addition, reduction, and metal-catalyzed coupling reactions, making it a practical building block for complex heterocyclic systems and pharmaceutical intermediates.
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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
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: