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Structure of 1794-48-5
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(3-Bromoprop-1-yn-1-yl)benzene features a terminal alkyne tethered to an aryl ring, enabling efficient copper-catalyzed coupling reactions. The bromine atom provides a reactive handle for nucleophilic substitution, while the propargylic position supports click chemistry applications. This compound delivers high functional group tolerance and stability under standard conditions, facilitating modular synthesis in medicinal chemistry and materials science.
(3-Bromoprop-1-yn-1-yl)benzene serves as a versatile synthetic building block for Sonogashira coupling reactions, enabling efficient access to conjugated alkynes and functionalized arylacetylenes. The terminal alkyne functionality exhibits excellent stability under standard bench conditions and demonstrates broad compatibility with various functional groups, facilitating straightforward purification and integration into complex molecular architectures. Its reactivity profile supports applications in the construction of heterocyclic scaffolds and advanced intermediates for medicinal chemistry and materials science.
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GHS No : GHS02,GHS05,GHS07,GHS08
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Signal Word : Danger
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UN#: 1294
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Class : 3
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Packing Group : Ⅱ
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Hazard Statements : H225-H302-H304-H315-H318-H336-H361-H373-H412
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P260-P261-P264-P270-P271-P273-P280-P302+P352-P304+P340-P330-P331-P362+P364-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: