CHEMICAL AND PHYSICAL PROPERTIES
Physical Description | Solid |
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Melting Point | 238-242 °C |
Solubility | 1.68e-01 g/L |
LogP | 2.9 |
Optical Rotation | Specific optical rotation: -193 °C at 25 °C/D |
Decomposition | When heated to decomposition material emits toxic fumes of /nitrogen oxides, hydrogen fluoride, hydrogen chloride/. /Moxifloxacin hydrochloride/ |
Dissociation Constants | 9.14 |
Collision Cross Section | 198.5 Ų [M+H]+ [CCS Type: TW, Method: calibrated with Waters Major Mix] |
Other Experimental Properties | Slightly yellow to yellow crystalline powder, mp 324-325 °C (decomposes), specific optical rotation: -256 °C at 25 °C/D (c = 0.5 in water) /Moxifloxacin hydrochloride/ |
COMPUTED DESCRIPTORS
Molecular Weight | 401.4 g/mol |
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XLogP3 | 0.6 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 4 |
Exact Mass | 401.17508442 g/mol |
Monoisotopic Mass | 401.17508442 g/mol |
Topological Polar Surface Area | 82.1 Ų |
Heavy Atom Count | 29 |
Formal Charge | 0 |
Complexity | 727 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 2 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Moxifloxacin is a quinolone that consists of 4-oxo-1,4-dihydroquinoline-3-carboxylic acid bearing a cyclopropyl substituent at position 1, a fluoro substitiuent at position 6, a (4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl group at position 7 and a methoxy substituent at position 8. A member of the fluoroquinolone class of antibacterial agents. It has a role as an antibacterial drug. It is a quinolinemonocarboxylic acid, a quinolone, a member of cyclopropanes, a pyrrolidinopiperidine, an aromatic ether, a quinolone antibiotic and a fluoroquinolone antibiotic. It is a conjugate base of a moxifloxacinium(1+).