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| | 1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4 -oxo-quinoline-3-carboxylic acid Basic information |
| Product Name: | 1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4 -oxo-quinoline-3-carboxylic acid | | Synonyms: | 1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4 -oxo-quinoline-3-carboxylic acid;3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-8-Methoxy-7-(octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-4-oxo-;N-Methyl Moxifloxacin HCl;N- methyl moxifloxacin hydrochloride;DL-Moxifloxacin;7-(1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl)-1-cyclopropyl-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylicaci;7-(1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl)-1-cyclopropyl-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid;1-cyclopropyl-6-fluoro-8-methoxy-7-(octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | | CAS: | 354812-41-2 | | MF: | C21H24FN3O4 | | MW: | 401.43 | | EINECS: | | | Product Categories: | | | Mol File: | 354812-41-2.mol | ![1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4 -oxo-quinoline-3-carboxylic acid Structure](CAS/GIF/354812-41-2.gif) |
| | 1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4 -oxo-quinoline-3-carboxylic acid Chemical Properties |
| Melting point | >141°C (dec.) | | Boiling point | 636.4±55.0 °C(Predicted) | | density | 1.408±0.06 g/cm3(Predicted) | | storage temp. | Refrigerator | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Solid | | pka | 6.43±0.50(Predicted) | | color | Pale Beige to Yellow |
| | 1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4 -oxo-quinoline-3-carboxylic acid Usage And Synthesis |
| Uses | 1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4-oxo-quinoline-3-carboxylic acid can be used as an intermediate in organic synthesis and Pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes. | | Synthesis |  1.Load a mixture of corresponding acid derivative (3.5 mmol) with piperazine (5.25mmol) in a small flask fitted with a micro condenser, placed in the microwave reactor.2. Irradiate the reaction mixture for 25 minutes at 150°C under solvent free conditions.
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| | 1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4 -oxo-quinoline-3-carboxylic acid Preparation Products And Raw materials |
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