2-(8-Fluoro-3-(2-methoxy-5-(trifluoromethyl)phenyl)-2-oxo-1,2,3,4-tetrahydroquinazolin-4-yl)acetic acid
Letermovir Impurity 1 is a fully characterized chemical compound used as a reference standard of API Letermovir. The standard offered is compliant with regulatory guidelines. Letermovir Impurity 1 is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 2991059-69-7
