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Structure of 78712-62-6
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Ethyl 6-bromo-2,2-dimethylhexanoate features a brominated aliphatic chain with a sterically hindered gem-dimethyl group, enabling selective functionalization in synthetic sequences. This bench-stable ester integrates readily into carbon–carbon bond-forming reactions and serves as a robust precursor for complex alkylated intermediates under mild conditions.
Ethyl 6-bromo-2,2-dimethylhexanoate serves as a versatile building block in synthetic organic chemistry, enabling the construction of complex alkylated scaffolds via palladium-catalyzed cross-coupling reactions. The bromide functionality offers high reactivity in Suzuki, Stille, and Negishi couplings, while the sterically hindered gem-dimethyl group enhances stability under standard reaction conditions. Its bench-stable nature and straightforward purification profile make it well-suited for iterative synthesis workflows 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: