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Structure of 1638744-20-3
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This fluorinated cyclopropane derivative features a chiral amine core with enhanced metabolic stability. The fluorine atom at the 2-position imparts conformational rigidity and modulates electronic properties, enabling precise control in medicinal chemistry applications. Delivers a potent bioisostere for amino acid side chains.
(1S,2S)-2-Fluorocyclopropan-1-amine hydrochloride serves as a conformationally constrained chiral building block for medicinal chemistry and catalytic synthesis. Its fluorinated cyclopropane core imparts metabolic stability and enhances binding affinity in bioactive molecules. The amine functionality enables straightforward derivatization via alkylation, acylation, or reductive amination, while the hydrochloride salt ensures excellent bench stability and ease of handling. This compound functions as a key scaffold in the synthesis of fluorinated analogs of biologically active compounds.
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Lot numbers can be found on the outside label of a product: