1-cyclopropyl-6,7-difluoro-1,4-dihydro-8- methoxy-4-oxo-3-quinolinecarboxylic acid

Product Name 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8- methoxy-4-oxo-3-quinolinecarboxylic acid
Alternate Names Moxifloxacin Impurities, Impurities of Moxifloxacin
CAT No. CS-O-31381
CAS No. 112811-72-0
Category Impurities
Stock IN-Stock
Mol. Wt. 295.24 g/mol
Mol. For. C₁₄H₁₁F₂NO₄
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Moxifloxacin
Purity >98%
Therapeutic Antibiotics
Smileys O=C(C1=CN(C2CC2)C3=C(C=C(F)C(F)=C3OC)C1=O)O
Canonical Smiles COC1=C2C(=CC(=C1F)F)C(=O)C(=CN2C3CC3)C(=O)O
InchIKey WQJZXSSAMGZVTM-UHFFFAOYSA-N
Inchl InChI=1S/C14H11F2NO4/c1-21-13-10(16)9(15)4-7-11(13)17(6-2-3-6)5-8(12(7)18)14(19)20/h4-6H,2-3H2,1H3,(H,19,20)
IUPAC 1-cyclopropyl-6,7-difluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid
Controlled No
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1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid is an important and potent antibiotic agent belonging to the fluoroquinolone class of compounds. It is a broad-spectrum antibiotic that is effective against both Gram-positive and Gram-negative bacteria. This compound is used in the treatment of various bacterial infections such as urinary tract infections, respiratory tract infections, skin infections, and gastrointestinal infections. Chemically, this compound is a derivative of quinolinecarboxylic acid and contains two fluoro and one methoxy substituent on the quinoline ring. It also contains a cyclopropyl group at position 1, which enhances its antibacterial activity. The mechanism of action of this compound involves inhibition of bacterial DNA gyrase and topoisomerase IV, which are essential enzymes involved in DNA replication and repair. The chemical formula of this compound is C17H15F2N2O4, and its molecular weight is 356.31 g/mol. It is a white to off-white powder that is soluble in water and organic solvents such as ethanol and methanol. The compound is stable under normal conditions of use and storage. In conclusion, 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid is a potent antibiotic agent that has a broad spectrum of activity against various bacterial infections. Its chemical structure contains important functional groups that enhance its antibacterial activity, and its mechanism of action involves inhibition of bacterial DNA replication and repair enzymes.

Related Compounds

N-Nitroso-Moxifloxacin | N-Nitroso Moxifloxacin Related compound-B | N-Nitroso Moxifloxacin Related compound-D | Moxifloxacin EP Impurity D | N-Nitroso Desmethyl Moxifloxacin methyl ester | Moxifloxacin EP Impurity D HCl salt | Moxifloxacin Impurity 2 | Moxifloxacin Nitroso Impurity 2 | N-Nitroso Moxifloxacin Related compound-C | N-Methyl Moxifloxacin Hydrochloride | Moxifloxacin Related Compound G HCl salt | Moxifloxacin Nitroso impurity 4 | Moxifloxacin Nitroso impurity 1 ( R,R Isomer) | Moxifloxacin N-methyl Impurity | Mono-Nitroso-Pyrrolopiperidine | Moxifloxacin Related Compound H | Moxifloxacin Hydrochloride Monohydrate | Moxifloxacin Related Compound F | Moxifloxacin Impurity 1 | ent-Moxifloxacin Hydrochloride | Moxifloxacin Nitroso impurity 3 ( R,R Isomer) | Moxifloxacin Impurity D Hydrochloride (8-Fluoro-6-Methoxy Moxifloxacin) | Moxifloxacin Methyl Ester | Moxifloxacin Impurity 69 | N-formyl moxifloxacin | Moxifloxacin Nitroso impurity 2 ( R,R Isomer) | Moxifloxacin EP impurity E | Moxifloxacin Nitroso R,R Isomer impurity | Moxifloxacin EP impurity B | N-Nitroso Moxifloxacin methyl ester | N-Allyloxycarbonyl Moxifloxacin | N-Nitroso Moxifloxacin Related compound-A | Moxifloxacin Impurity 38 | Di-Nitroso- Pyrrolopiperidine | Moxifloxacin EP Impurity A | Moxifloxacin Difluoro Hydroxy Impurity | Moxifloxacin Related Compound B |

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