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Structure of 128312-69-6
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2-Bromo-1-cyclobutylethanone features a bromine-substituted ketone tethered to a cyclobutyl ring, delivering a reactive handle for nucleophilic substitution and transition metal-catalyzed coupling. This sterically constrained scaffold enables efficient integration into complex molecular architectures under mild conditions.
2-Bromo-1-cyclobutylethanone serves as a versatile building block for constructing cyclobutyl-containing heterocycles and functionalized alkyl chains. Its α-bromoketone motif enables direct nucleophilic substitution, enolate formation, and transition-metal-catalyzed coupling reactions. The molecule exhibits bench stability and facilitates straightforward purification, 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
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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 : Ⅱ
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Hazard Statements : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: