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Structure of 61765-46-6
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3-Iodocyclopent-2-en-1-one features a reactive iodine substituent at the C3 position of a cyclopentenone ring, enabling direct functionalization in cross-coupling reactions. The conjugated enone system enhances electrophilicity, facilitating nucleophilic attack or transition-metal-catalyzed transformations under mild conditions. This structure combines synthetic accessibility with high reactivity, making it a valuable intermediate for complex molecule assembly.
3-Iodocyclopent-2-en-1-one serves as a versatile building block for transition-metal-catalyzed couplings, enabling efficient access to functionalized cyclopentane scaffolds. Its iodine moiety facilitates palladium- and copper-mediated transformations with high chemoselectivity, while the enone system supports conjugate additions and Diels–Alder reactions. The compound exhibits good bench stability and is readily purified by flash chromatography, making it well-suited for iterative synthesis in medicinal chemistry and natural product 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: