
CAS 110548-07-7
:Formule :C13H9F2NO4
InChI :InChI=1S/C13H9F2NO4/c1-5-4-20-12-9(15)8(14)2-6-10(12)16(5)3-7(11(6)17)13(18)19/h2-3,5H,4H2,1H3,(H,18,19)/t5-/m1/s1
Code InChI :NVKWWNNJFKZNJO-RXMQYKEDSA-N
SMILES :C[C@@H]1COC2=C3N1C=C(C(=O)C3=CC(=C2F)F)C(=O)O
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6 produits trouvés.
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Levofloxacin Impurity 8
CAS :Formule :C13H9F2NO4Couleur et forme :White To Off-White Solid SolidMasse moléculaire :281.22(3R)-9,10-Difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid (>85%)
CAS :Produit contrôléApplications (3R)-9,10-Difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid is an intermediate in the synthesis of Ofloxacin (O245750), an fluorinated quinolone based antibacterial agent.
References Mitscher, L. A., et la.: J. Med. Chem., 30, 2283 (1987);Formule :C13H9F2NO4Degré de pureté :>85%Couleur et forme :NeatMasse moléculaire :281.21(R)-Ofloxacin Carboxylic Acid (Dextrofloxacin Difluoro Impurity)
CAS :Produit contrôléFormule :C13H9F2NO4Couleur et forme :NeatMasse moléculaire :281.21Ofloxacin Q acid
CAS :Ofloxacin Q acid is a quinolone analog, which is a synthetic derivative known for its significant antibacterial properties. This compound is sourced from the chemical synthesis of fluoroquinolone derivatives, designed to enhance reactivity and efficacy in pharmaceutical applications. Ofloxacin Q acid acts by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes critical for DNA replication, transcription, and repair, thereby leading to the cessation of bacterial growth and replication.Formule :C13H9F2NO4Degré de pureté :Min. 95%Masse moléculaire :281.21 g/molR-Ofloxacin Q Acid
CAS :Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFormule :C13H9F2NO4Masse moléculaire :281.04996





