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Structure of 1257535-00-4
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6-Amino-2-bromo-3-fluorophenol features a strategically positioned amino group enabling direct functionalization in medicinal chemistry. The bromine and fluorine substituents provide orthogonal reactivity and enhanced metabolic stability. This electron-deficient scaffold supports palladium-catalyzed couplings and integrates readily into bioactive heterocycles under standard conditions.
6-Amino-2-bromo-3-fluorophenol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at multiple sites due to its ortho-halogen and amino groups. The bromo group facilitates Suzuki-Miyaura and Stille couplings, while the amino functionality supports acylation, alkylation, and diazotization reactions. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds and API intermediates in multi-step syntheses.
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Lot numbers can be found on the outside label of a product: