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Structure of 617-33-4
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Ethyldibromoacetate serves as a bifunctional alkylating agent, featuring two bromine atoms on the α-carbon that enable sequential substitution reactions. This reactivity facilitates efficient carbon–carbon bond formation in synthetic pathways, particularly in the construction of cyclic systems and functionalized intermediates under mild conditions. The ethyl ester group enhances solubility and compatibility with organic solvents, supporting broad utility in medicinal chemistry and materials synthesis.
Ethyldibromoacetate serves as a versatile dihaloacetic ester reagent, enabling efficient α-alkylation and functionalization of carbonyl compounds via enolization. Its dual bromine atoms facilitate sequential substitution reactions, particularly in the synthesis of substituted acetic acid derivatives and heterocyclic scaffolds. The compound exhibits good bench stability and is compatible with standard organic workups, making it a practical choice for iterative synthetic transformations in medicinal chemistry and process development.
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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-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: