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Structure of 54932-72-8
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4-Bromo-1-chloro-2-methylbenzene features a strategically positioned bromo and chloro substituent on a methylated benzene ring, enabling selective cross-coupling reactions. The ortho-methyl group enhances regioselectivity in palladium-catalyzed transformations, while the halogen array supports sequential functionalization under mild conditions. This electron-deficient aryl scaffold delivers high reactivity with minimal side-product formation.
4-Bromo-1-chloro-2-methylbenzene serves as a versatile building block in cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its orthogonal halogen reactivity—bromine undergoing palladium-catalyzed coupling while chloride remains inert—facilitates sequential functionalization. The methyl group provides a site for further oxidation or directed metallation, enhancing synthetic versatility. Bench-stable and readily purified by distillation, it supports scalable synthesis in medicinal chemistry and materials development.
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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: