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5-Fluoro-2-methoxy-4-pyridinamine is a model compound that is used for the acetylation of nucleosides and alkylation of pentofuranosyl groups. It is an acetylated, dealkylated, and hydrochloride salt form of 5-fluoro-2-methoxy-4-pyridinamine. The chloride salt form of this compound can be used to synthesize nucleoside analogues that are resistant to viral replication.