ChemicalBook--->CAS DataBase List--->101363-10-4

101363-10-4

101363-10-4 Structure

101363-10-4 Structure
IdentificationBack Directory
[Name]

RUFLOXACIN
[CAS]

101363-10-4
[Synonyms]

Qari
Mones
Tebraxin
ISF-09334
RUFLOXACIN
4]thiazino[2
AKOS NCG1-0068
3-dihydro-7H-[1
RUFLOXACIN USP/EP/BP
4-ij]quinoline-6-carboxylic acid
9-Fluoro-10-(4-methylpiperazin-1-yl)-7-oxo-2
8-FLUORO-9-(4-METHYL-PIPERAZIN-1-YL)-6-OXO-2,3-DIHYDRO-6H-1-THIA-3A-AZA-PHENALENE-5-CARBOXYLIC ACID
9-Fluom-2,3-dihydro-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzothiazine-6-carboxylic acid
9-Fluoro-2,3-dihydro-10-(4-methylpiperazin-1-yl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzothiazine-6-carboxylic acid
7H-Pyrido[1,2,3-de]-1,4-benzothiazine-6-carboxylic acid, 9-fluoro-2,3-dihydro-10-(4-methyl-1-piperazinyl)-7-oxo-
[Molecular Formula]

C17H18FN3O3S
[MDL Number]

MFCD00865073
[MOL File]

101363-10-4.mol
[Molecular Weight]

363.41
Chemical PropertiesBack Directory
[Boiling point ]

574.6±50.0 °C(Predicted)
[density ]

1.54
[storage temp. ]

2-8°C
[pka]

5.21±0.20(Predicted)
[CAS DataBase Reference]

101363-10-4
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H302-H315-H319
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Triethylamine-->Ammonium chloride-->N,N-Dimethylformamide dimethyl acetal-->Ethyl benzoylacetate-->1,2,3-Trifluoro-4-nitrobenzene-->2-Quinolinol-->ETHYL THIOGLYCOLATE-->2-Mercaptoethanol-->2,3,4,5-Tetrafluorobenzoic acid-->thiazine-->2,3,4-TRICHLORONITROBENZENE-->Rufloxacin hydrochloride-->3-CHLORO-2,4-DIFLUORONITROBENZENE
Hazard InformationBack Directory
[Definition]

ChEBI: Rufloxacin is a member of quinolines, a quinolone antibiotic and a fluoroquinolone antibiotic.
[Pharmaceutical Applications]

A tricyclic fluoroquinolone formulated as the hydrochloride salt. It is inactive against Gram-positive cocci with MICs >2 mg/L. It displays weak activity in vitro against Enterobacteriaceae with the MIC for most species >1 mg/L. Activity against Ps. aeruginosa is poor (MIC 16–32 mg/L). After loading doses of 400 and 600 mg followed with 9 days of either 200 or 300 mg, mean peak plasma levels were around 4.5–7 mg/L, respectively. The mean apparent elimination halflife was 44 h. Approximately 50% is eliminated in the urine.
It has been used in urinary tract infection and chronic prostatitis, but clinical experience is limited.
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