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Structure of 502-49-8
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Cyclooctanone features a strained eight-membered carbonyl ring, offering enhanced reactivity in cycloaddition and metal-catalyzed transformations. This bench-stable ketone serves as a key intermediate in synthesizing complex cyclic architectures and natural product analogs.
Cyclooctanone serves as a versatile cyclic ketone scaffold in organic synthesis, enabling stereoselective transformations via enolate chemistry and facilitating ring-functionalization reactions. Its eight-membered ring structure provides moderate strain, supporting ring-opening and cycloaddition processes under controlled conditions. The carbonyl group exhibits high reactivity in nucleophilic additions and acts as a key handle for derivatization, including reductive amination and oxime formation. Bench-stable and readily purified by distillation or recrystallization, Cyclooctanone functions as a reliable building block for complex molecular architectures in medicinal chemistry and materials science.
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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#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: