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Structure of 2235-15-6
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Acenaphthylen-1(2H)-one features a reactive ketone moiety flanked by a rigid, fused polycyclic framework, enabling its use in Diels-Alder reactions and as a building block for functionalized heterocycles. The molecule exhibits enhanced stability under standard conditions while maintaining high reactivity at the carbonyl site.
Acenaphthylen-1(2H)-one serves as a versatile building block in synthetic organic chemistry, enabling access to polycyclic aromatic frameworks and heterocyclic systems. Its reactive enone functionality facilitates conjugate additions, Diels-Alder cycloadditions, and transition-metal-catalyzed coupling reactions. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it well-suited for scalable synthesis and medicinal chemistry applications.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: