(R)-Ofloxacin

Product Name (R)-Ofloxacin
CAT No. CS-T-59876
CAS No. 100986-86-5
Category Impurities
Stock IN-Stock
Mol. Wt. 361.37 g/mol
Mol. For. C₁₈H₂₀FN₃O₄
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys CC1COC2=C3N1C=C(C(=O)C3=CC(=C2N4CCN(CC4)C)F)C(=O)O
Canonical Smiles CC1COC2=C3N1C=C(C(=O)C3=CC(=C2N4CCN(CC4)C)F)C(=O)O
InchIKey GSDSWSVVBLHKDQ-SNVBAGLBSA-N
Inchl InChI=1S/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/t10-/m1/s1
IUPAC (2R)-7-fluoro-2-methyl-6-(4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8,11-tetraene-11-carboxylic acid
Controlled No
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(R)-Ofloxacin is a fluoroquinolone antibiotic that is used to treat various bacterial infections. It is the active enantiomer of Ofloxacin, which means it is the mirror image of the compound that is commonly used. This enantiomer has been found to be more effective in treating bacterial infections than its counterpart. (R)-Ofloxacin works by inhibiting the activity of enzymes that are essential for bacterial growth and replication. This antibiotic is effective against a wide range of bacteria, including Gram-positive and Gram-negative bacteria. It is commonly used to treat urinary tract infections, respiratory infections, and skin infections. The chemical structure of (R)-Ofloxacin consists of a pyridine ring, a fluorine atom, and a carboxylic acid group. It has a molecular weight of 361.4 g/mol and a melting point of 290-300°C. (R)-Ofloxacin is soluble in water, dimethyl sulfoxide, and ethanol. It is important to note that (R)-Ofloxacin should not be used in patients with a history of hypersensitivity to fluoroquinolones. It may also interact with other medications, so it is important to inform your healthcare provider of any other medications you may be taking. In conclusion, (R)-Ofloxacin is a powerful and effective antibiotic that is commonly used to treat bacterial infections. Its chemical structure and mechanism of action make it a valuable tool in the fight against bacterial infections.

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