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Structure of 7778-01-0
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1-(Bromomethyl)-3,5-dichlorobenzene features a reactive bromomethyl group flanked by two electron-withdrawing chloro substituents, enabling efficient coupling reactions in synthetic sequences. This bench-stable aryl halide integrates readily into cross-coupling and nucleophilic substitution processes, offering predictable reactivity for building complex molecular architectures under standard conditions.
1-(Bromomethyl)-3,5-dichlorobenzene serves as a versatile benzylating agent in synthetic organic chemistry, enabling efficient introduction of the 3,5-dichlorobenzyl group into diverse substrates. The bromomethyl functionality reacts readily with nucleophiles under mild conditions, offering high chemoselectivity and compatibility with common functional groups. Its bench-stable nature and ease of purification make it well-suited for multi-step synthesis, including the construction of heterocyclic scaffolds and bioactive intermediates in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: