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Structure of 1518-06-5
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1,3-Dibromo-3-methylbutan-2-one features a sterically hindered ketone scaffold flanked by two bromine atoms, enabling selective electrophilic functionalization. This bench-stable reagent integrates readily into synthetic sequences requiring controlled halogenation or carbon–carbon bond formation under mild conditions.
1,3-Dibromo-3-methylbutan-2-one serves as a versatile synthetic intermediate for constructing brominated heterocycles and functionalized ketones. Its α-brominated carbonyl structure enables efficient alkylation and nucleophilic substitution reactions under mild conditions. The molecule exhibits good bench stability and facilitates clean transformations with minimal side products, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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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 : H302-H312-H314-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P330+P331-P302+P352-P304+P340-P330-P362+P364-P363-P405-P501
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Lot numbers can be found on the outside label of a product: