Antioxidant BHT 264
CAS:128-37-0
Purity:99%
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Manufacturer supply high quality Moxifloxacin HCL 186826-86-8 with ISO standards We supply high quality Moxifloxacin hydrochloride (CAS 186826-86-8), in stock, factory directly supply to clients, lower prices, more competitiveness.
Moxifloxacin hydrochloride is 99%, while it's Molecular Formula is C21H24FN3O4.ClH. An antibacterial agent that inhibits the activities of Topo II (DNA gyrase) and topoisomerase IV
The CAS number of Moxifloxacin hydrochloride is 186826-86-8.
More information of Moxifloxacin hydrochloride 186826-86-8 are:
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Synonyms |
Moxifloxacin HCl;3-Quinolinecarboxylicacid,1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-,hydrochloride (1:1);3-Quinolinecarboxylic acid,1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-,monohydrochloride (9CI);Actira;Avalox;Avelox;BAY 12-8039;Lapinix;Octegra; |
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CAS Number |
186826-86-8 |
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Molecular Formula |
C21H24FN3O4.ClH |
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Molecular Weight |
437.899 |
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Melting Point |
Slightly yellow to yellow crystalline powder, mp 324-325° |
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Boiling Point |
636.4 °C at 760 mmHg |
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Flash Point |
338.7 °C |
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HS CODE |
2933499090 |
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PSA |
83.80000 |
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LogP |
3.56630 |
Moxifioxacin hydrochlodde is one of the two new fluoroquinolonecarboxylic acid antibiotics introduced in 1999 for the treatment of respiratory tract infections such as community-acquired pneumonia, acute exacerbations of bronchitis or acute sinusitis. Moxifloxacin can be synthesized through a 12 step sequence from the classical 4-quinolone-3-carboxylic acid template. Some advantages of Moxifloxacin over Ciprofloxacin, another of Bayer's launched quinolones, have been shown, i.e. an enhanced activity against Gram-positive bacteria (Streptococcus pneumoniae, Clostndium pneumoniae), a favorable pharmacokinetic profile (good tissue penetration and plasma concentrations above MICs) and a lack of phototoxicity (UVA irradiation).
InChI:InChI=1/C21H24FN3O4.ClH/c1-29-20-17-13(19(26)14(21(27)28)9-25(17)12-4-5-12)7-15(22)18(20)24-8-11-3-2-6-23-16(11)10-24;/h7,9,11-12,16,23H,2-6,8,10H2,1H3,(H,27,28);1H
Articles related to Moxifloxacin hydrochloride:
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Article |
Source |
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Preparation method of quinolone carboxylic acid derivative or phthalazinone carboxylic acid derivative |
- Paragraph 0065-0067; 0074-0076; 0107-0180, (2021/10/27) |
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Preparation method of moxifloxacin hydrochloride (by machine translation) |
- Paragraph 0032; 0035; 0038; 0041; 0044; 0047; 0048; 0051, (2020/12/14) |
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