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Structure of 2327-69-7
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Ethyl 4-(diethoxyphosphoryl)butanoate features a reactive phosphonate ester group flanked by a flexible aliphatic chain, enabling efficient coupling in Pudovin-type reactions. This bench-stable reagent integrates readily into synthetic sequences requiring controlled C–C bond formation, offering high functional group tolerance and straightforward handling under standard conditions.
Ethyl 4-(diethoxyphosphoryl)butanoate serves as a versatile synthon in carbonyl-alkylation and Michael addition strategies, enabling efficient construction of γ- and δ-functionalized carboxylates. Its diethylphosphoryl group facilitates nucleophilic displacement and acts as a masked acyl equivalent, while the ester functionality supports orthogonal transformations. Bench-stable and readily purified by distillation, it functions reliably in standard synthetic workflows for complex molecule assembly.
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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
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Precautionary Statements : P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: