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Structure of 188472-71-1
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4-Chloro-1-ethynyl-2-fluorobenzene features a strategically positioned ethynyl group flanked by electron-withdrawing chlorine and fluorine substituents, enabling efficient coupling in palladium-catalyzed cross-coupling reactions. This bench-stable aryl acetylene integrates readily into complex molecular architectures, offering high functional group tolerance and predictable reactivity in synthetic workflows.
4-Chloro-1-ethynyl-2-fluorobenzene serves as a versatile building block in transition-metal-catalyzed coupling reactions, enabling efficient access to substituted biaryls and conjugated systems. The ortho-fluoro and chloro substituents provide orthogonal reactivity for sequential functionalization, while the terminal alkyne facilitates Sonogashira, Glaser, or Huisgen cycloadditions. Bench-stable and readily purified by column chromatography, it supports scalable synthesis of complex scaffolds relevant to medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1325
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Class : 4.1
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Packing Group : Ⅲ
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Hazard Statements : H228-H315-H319-H335
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Precautionary Statements : P210-P240-P241-P280-P370+P378
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Lot numbers can be found on the outside label of a product: