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Structure of 919017-55-3
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This oxadiazole derivative features a 2-fluorophenyl group conjugated to a methanamine side chain, delivering enhanced electron-withdrawing character and improved solubility. The para-fluoro substitution stabilizes the aromatic system while facilitating downstream functionalization. Ideal for medicinal chemistry applications requiring metabolic stability and targeted binding.
(3-(2-Fluorophenyl)-1,2,4-oxadiazol-5-yl)methanamine serves as a versatile building block for medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling reactions. Its oxadiazole core offers enhanced metabolic stability and favorable polarity, while the primary amine facilitates conjugation with carboxylic acids, aldehydes, or isocyanates. Bench-stable and readily purified by chromatography, it functions effectively in parallel synthesis campaigns targeting CNS-directed therapeutics and kinase inhibitors.
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Lot numbers can be found on the outside label of a product: