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Structure of 1235479-59-0
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3-Ethylbicyclo[3.2.0]hept-3-en-6-one features a strained bicyclic framework with a conjugated enone system, enabling efficient Diels-Alder cycloadditions. The ethyl substituent at the bridgehead position enhances regiochemical control in asymmetric synthesis, while the ketone moiety serves as a handle for selective functionalization. This structure combines high reactivity with predictable stereochemical outcomes.
3-Ethylbicyclo[3.2.0]hept-3-en-6-one serves as a versatile bicyclic enone scaffold for synthetic applications in natural product and medicinal chemistry. Its conjugated enone system enables reliable Michael additions, Diels–Alder cycloadditions, and functionalization at the C3 position. Bench-stable and readily purified by flash chromatography, it functions as a key building block for complex terpene-like architectures and heterocyclic systems requiring defined stereochemistry and ring strain.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: