{(S)-8-fluoro-2-[4-(m-hydroxyphenyl)-1-piperazinyl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-3,4-dihydro-4-quinazolinyl}acetic acid
Letermovir Impurity 3 is a fully characterized chemical compound used as a reference standard of API Letermovir. The standard offered is compliant with regulatory guidelines. Letermovir Impurity 3 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 - NA
