
CAS 110548-07-7
:Fórmula: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
Clave InChI:NVKWWNNJFKZNJO-RXMQYKEDSA-N
SMILES:C[C@@H]1COC2=C3N1C=C(C(=O)C3=CC(=C2F)F)C(=O)O
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Levofloxacin Impurity 8
CAS:Fórmula:C13H9F2NO4Forma y color:White To Off-White Solid SolidPeso molecular: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:Producto controladoApplications (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);Fórmula:C13H9F2NO4Pureza:>85%Forma y color:NeatPeso molecular:281.21(R)-Ofloxacin Carboxylic Acid (Dextrofloxacin Difluoro Impurity)
CAS:Producto controladoFórmula:C13H9F2NO4Forma y color:NeatPeso molecular: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.Fórmula:C13H9F2NO4Pureza:Min. 95%Peso molecular:281.21 g/molR-Ofloxacin Q Acid
CAS:Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFórmula:C13H9F2NO4Peso molecular:281.04996





