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Structure of 1638744-40-7
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This difluoromethyl-substituted pyrrolidine hydrochloride features a conformationally constrained heterocycle with enhanced metabolic stability. The electron-withdrawing difluoromethyl group modulates basicity and lipophilicity, enabling improved membrane permeability. This bench-stable salt form facilitates handling in synthetic workflows, particularly in medicinal chemistry campaigns targeting CNS-penetrant molecules.
(3S)-3-(Difluoromethyl)pyrrolidine hydrochloride serves as a versatile chiral building block in medicinal chemistry, enabling the introduction of a difluoromethyl group at the pyrrolidine C3 position. Its bench-stable hydrochloride salt form facilitates handling and purification, while the stereodefined (3S) configuration supports predictable reactivity in asymmetric synthesis. The difluoromethyl moiety enhances metabolic stability and modulates lipophilicity, making this scaffold valuable for optimizing pharmacokinetic properties in bioactive molecules.
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Lot numbers can be found on the outside label of a product: