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Structure of 1260810-06-7
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5-Bromo-3-chloro-2-hydroxybenzonitrile features a unique trifunctional aromatic core with bromo, chloro, hydroxy, and nitrile groups in close proximity. This electron-deficient scaffold enables selective coupling reactions under mild conditions, facilitating rapid access to complex heterocycles. The hydroxy group enhances solubility and serves as a handle for derivatization, while the nitrile moiety offers synthetic versatility. Bench-stable and moisture-tolerant, this compound streamlines late-stage functionalization in medicinal chemistry and materials synthesis.
5-Bromo-3-chloro-2-hydroxybenzonitrile serves as a versatile building block in medicinal chemistry, enabling the construction of substituted heterocycles via nucleophilic aromatic substitution or transition-metal-catalyzed coupling. The hydroxyl group facilitates downstream derivatization, while the nitrile and halogen functionalities offer orthogonal reactivity for further functionalization. Bench-stable and compatible with standard purification protocols, it supports scalable synthesis of complex scaffolds.
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Lot numbers can be found on the outside label of a product: