Synthetic Route of 100491-29-0, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.100491-29-0, Name is Ethyl 7-chloro-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate, molecular formula is C17H10ClF3N2O3. In a Patent£¬once mentioned of 100491-29-0
Pfizer Inc.
Antibacterial quinolone carboxylic acids and naphthyridone carboxylic acids, having an external amino group attached to their 7-substituent are prepared without the use, and subsequent removal, of blocking groups on the external amino group. In a preferred embodiment, the naphthyridone carboxylic acid is the antibiotic trovafloxacin.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 100491-29-0, and how the biochemistry of the body works.Synthetic Route of 100491-29-0
Reference£º
1,777-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N771 – PubChem