Introduction:Basic information about CAS 1269726-67-1|Dapaconazole, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Dapaconazole |
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| CAS Number | 1269726-67-1 | Molecular Weight | 415.236 |
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| Density | 1.4±0.1 g/cm3 | Boiling Point | 512.8±50.0 °C at 760 mmHg |
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| Molecular Formula | C19H15Cl2F3N2O | Melting Point | / |
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| MSDS | / | Flash Point | 263.9±30.1 °C |
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Names
| Name | dapaconazole |
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| Synonym | More Synonyms |
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Dapaconazole BiologicalActivity
| Description | Dapaconazole, as an antifungal agent, inhibits sterol 14α-demethylase cytochrome P450 activity with an IC50 of 1.4 μM[1]. |
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| Related Catalog | Research Areas >>InfectionSignaling Pathways >>Metabolic Enzyme/Protease >>Cytochrome P450 |
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| Target | Cytochrome P450 (CYP26):1.4 μM (IC50) |
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| In Vitro | Dapaconazole inhibits sterol 14α-demethylase cytochrome P450 activity with an IC50 of 1.4 ± 0.3 μM[1]. |
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| In Vivo | Dapaconazole (20 mg/kg; p.o.) shows that the bioavailability is 97.3 %[1]. Animal Model: Male beagle dogs[1] Dosage: 20 mg/kg (Pharmacokinetic Analysis) Administration: P.o. Result: Showed that the bioavailability was 97.3 %. |
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| References | [1]. Juliana SP, et al. Pharmacokinetics of Dapaconazole, A Novel Antifungal Agent, in Beagle Dogs and Inhibition of Cytochrome P450 Family 51. J Eur Acad Dermatol Venereol. 2018 Jun 10. |
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Chemical & Physical Properties
| Density | 1.4±0.1 g/cm3 |
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| Boiling Point | 512.8±50.0 °C at 760 mmHg |
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| Molecular Formula | C19H15Cl2F3N2O |
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| Molecular Weight | 415.236 |
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| Flash Point | 263.9±30.1 °C |
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| Exact Mass | 414.051361 |
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| LogP | 5.30 |
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| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
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| Index of Refraction | 1.565 |
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| Storage condition | 2-8°C |
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Synonyms
| 1-[2-(2,4-Dichlorophenyl)-2-{[4-(trifluoromethyl)benzyl]oxy}ethyl]-1H-imidazole |
| dapaconazole |
| H2976538CX |
| 1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[[4-(trifluoromethyl)phenyl]methoxy]ethyl]- |
| UNII:H2976538CX |