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Structure of 1211512-31-0
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2-Bromo-6-chloro-3-methylphenol features a trifunctional aromatic core with bromo, chloro, and methyl substituents positioned for selective downstream coupling. The electron-withdrawing halogens enhance reactivity in cross-coupling processes, while the methyl group provides steric stabilization. This compound serves as a key intermediate in agrochemical and pharmaceutical synthesis, offering predictable regioselectivity under standard conditions.
2-Bromo-6-chloro-3-methylphenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling selective functionalization at the phenolic hydroxyl group. Its ortho-bromine and meta-chlorine substituents provide orthogonal reactivity for cross-coupling reactions, while the methyl group enhances lipophilicity and metabolic stability. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows and scale-up applications.
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Lot numbers can be found on the outside label of a product: