Loflucarban structure
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Common Name | Loflucarban | ||
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CAS Number | 790-69-2 | Molecular Weight | 315.19300 | |
Density | 1.531g/cm3 | Boiling Point | 395ºC at 760 mmHg | |
Molecular Formula | C13H9Cl2FN2S | Melting Point | N/A | |
MSDS | N/A | Flash Point | 192.7ºC |
Use of LoflucarbanLoflucarban (Fluonilid) is a potent antimycotic agent. Loflucarban can be used for the research of the ear infections[1]. |
Name | 1-(3,5-dichlorophenyl)-3-(4-fluorophenyl)thiourea |
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Synonym | More Synonyms |
Description | Loflucarban (Fluonilid) is a potent antimycotic agent. Loflucarban can be used for the research of the ear infections[1]. |
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Related Catalog | |
In Vitro | One hundred-and-eighty-six fungi were isolated from one hundred-and-eighty cases diagnosed as otomycosis. They comprise 59 species of 26 genera of moulds, and 2 genera of yeasts. Fluonilid shows the MIC ranged from > 100 μg/ml to 1 μg/ml for the majority of tested fungi[1]. |
References |
Density | 1.531g/cm3 |
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Boiling Point | 395ºC at 760 mmHg |
Molecular Formula | C13H9Cl2FN2S |
Molecular Weight | 315.19300 |
Flash Point | 192.7ºC |
Exact Mass | 313.98500 |
PSA | 56.15000 |
LogP | 5.08740 |
Index of Refraction | 1.729 |
Storage condition | -20℃ |
Loflucarban |
Loflucarbanum [Latin] |
Loflucarbanum |
Fluonilid |
Fluonilide |
3,5-Dichloro-4'-fluorothiocarbanilide |
Fluoro-4-dichloro-3',5'-thiocarbanilide |