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Structure of 3710-23-4
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2-(Prop-1-en-2-yl)naphthalene features a conjugated vinyl group attached directly to the naphthalene core, enabling efficient integration into Diels-Alder cycloadditions and other pericyclic reactions. The electron-rich aromatic system enhances reactivity in transition-metal-catalyzed coupling processes. This compound exhibits high thermal stability and is readily handled under standard laboratory conditions.
2-(Prop-1-en-2-yl)naphthalene serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized naphthalene derivatives via electrophilic addition and transition-metal-catalyzed coupling reactions. The exocyclic ene group exhibits high reactivity in Diels–Alder processes and allows for selective functionalization under mild conditions. Its bench-stable nature and compatibility with common protecting groups facilitate straightforward purification and integration into complex molecular architectures, making it a practical scaffold for medicinal chemistry and materials synthesis workflows.
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GHS Pictogram :
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GHS No : GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H361-H372-H410
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Precautionary Statements : P264-P280-P301+P330+P331
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Lot numbers can be found on the outside label of a product: