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Structure of 1695914-13-6
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This difluorocyclopentane derivative features a bromomethyl group enabling facile functionalization. The geminal difluoro substitution enhances metabolic stability and modulates lipophilicity, while the primary alkyl halide handles facilitate coupling reactions in synthetic workflows.
3-(Bromomethyl)-1,1-difluorocyclopentane serves as a versatile difluorinated alkylating agent, enabling efficient introduction of fluorinated side chains into complex molecular architectures. The bromomethyl group facilitates nucleophilic substitution reactions under mild conditions, while the 1,1-difluorocyclopentane core provides enhanced metabolic stability and lipophilicity—key attributes in medicinal chemistry. Its bench-stable nature and compatibility with diverse functional groups make it suitable for modular synthesis of fluorinated building blocks and bioactive scaffolds.
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Lot numbers can be found on the outside label of a product: