(S)-Flumequine

Base Information Edit

Chemical Name:(S)-Flumequine
CAS No.:202349-45-9
Molecular Formula:C₁₄H₁₂FNO₃
Molecular Weight:261.253
Hs Code.:
UNII:BRD84T215S
Nikkaji Number:J1.113.736I
Wikidata:Q27158448
Mol file:202349-45-9.mol

Synonyms:(S)-Flumequine;Flumequine, (S)-;202349-45-9;BRD84T215S;UNII-BRD84T215S;1H,5H-Benzo(ij)quinolizine-2-carboxylic acid, 9-fluoro-6,7-dihydro-5-methyl-1-oxo-, (5S)-;1H,5H-Benzo(ij)quinolizine-2-carboxylic acid, 9-fluoro-6,7-dihydro-5-methyl-1-oxo-, (S)-;(12S)-7-fluoro-12-methyl-4-oxo-1-azatricyclo[7.3.1.05,13]trideca-2,5,7,9(13)-tetraene-3-carboxylic acid;SCHEMBL49830;CHEBI:85272;PD132670;A11861;Q27158448;(5S)-9-fluoro-5-methyl-1-oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid

Suppliers and Price of (S)-Flumequine

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(S)-Flumequine
50mg
$ 1320.00

Total 8 raw suppliers

Chemical Property of (S)-Flumequine Edit

Chemical Property:

Boiling Point:439.7±45.0 °C(Predicted)
PKA:5.70±0.40(Predicted)
Density:1.45±0.1 g/cm3(Predicted)
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:261.08012141
Heavy Atom Count:19
Complexity:462

Purity/Quality:

99% ^*data from raw suppliers

(S)-Flumequine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1CCC2=C3N1C=C(C(=O)C3=CC(=C2)F)C(=O)O
Isomeric SMILES:C[C@H]1CCC2=C3N1C=C(C(=O)C3=CC(=C2)F)C(=O)O
Uses (S)-Flumequine, an isomer of Flumequine (F445000), a fluorinated quinolone antibacterial.

Technology Process of (S)-Flumequine

There total 20 articles about (S)-Flumequine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 77.5%