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Structure of 75717-77-0
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2,4-Dichloro-1-ethynylbenzene features a reactive alkyne handle flanked by two electron-withdrawing chlorine atoms, enabling efficient coupling in transition-metal-catalyzed transformations. This bench-stable arylacetylene integrates readily into conjugated frameworks and serves as a robust building block for functionalized arenes under standard conditions.
2,4-Dichloro-1-ethynylbenzene serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of conjugated biaryl and heteroaryl architectures. The ethynyl group facilitates Sonogashira coupling with aryl halides, while the dichloro substitution pattern supports sequential functionalization. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for iterative synthesis of complex scaffolds in medicinal chemistry and materials science.
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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: