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Structure of 1044256-89-4
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1-Bromo-3-(bromomethyl)-2-chlorobenzene features a bromomethyl group flanked by bromo and chloro substituents on a benzene ring, enabling orthogonal reactivity in multi-step synthesis. This arrangement supports selective functionalization under mild conditions, particularly in cross-coupling and nucleophilic substitution processes. The molecule’s steric and electronic profile facilitates controlled transformations without significant side reactions.
1-Bromo-3-(bromomethyl)-2-chlorobenzene serves as a versatile dihalogenated aromatic building block, enabling efficient construction of complex pharmaceutical intermediates. The bromomethyl group facilitates nucleophilic substitution and coupling reactions, while the ortho-bromo and meta-chloro substituents provide orthogonal reactivity for sequential functionalization. Bench-stable and compatible with standard cross-coupling protocols, it functions reliably in the synthesis of heterocyclic scaffolds and bioactive molecules.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: