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Structure of 1516698-94-4
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1-(2-Fluoroethyl)azetidin-3-amine features a strained azetidine ring bearing a primary amine and a 2-fluoroethyl substituent, delivering enhanced metabolic stability and improved membrane permeability. This combination enables efficient incorporation into bioactive molecules for medicinal chemistry applications.
1-(2-Fluoroethyl)azetidin-3-amine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through its reactive azetidine core and pendant fluorinated ethyl chain. The molecule exhibits favorable bench stability and functional group tolerance, facilitating straightforward incorporation into diverse synthetic sequences. Its bifunctional nature—combining a nucleophilic amine with a latent electrophilic fluorine—enables site-specific derivatization and strategic molecular diversification in API development workflows.
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Lot numbers can be found on the outside label of a product: