difenoconazole structure
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Common Name | difenoconazole | ||
|---|---|---|---|---|
| CAS Number | 119446-68-3 | Molecular Weight | 406.263 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 547.0±60.0 °C at 760 mmHg | |
| Molecular Formula | C19H17Cl2N3O3 | Melting Point | 76°C | |
| MSDS | Chinese USA | Flash Point | 284.6±32.9 °C | |
| Symbol |
GHS07, GHS09 |
Signal Word | Warning | |
Use of difenoconazoleDifenoconazole is a broad-spectrum triazole fungicide that inhibits ergosterol biosynthesis via inhibition of the cytochrome P450-dependent 14α-demethylation of lanosterol, which results in disruption of the fungal cell membrane and cell death. Difenoconazole inhibits the growth of F. graminearum isolates in vitro (EC50s = 1.69-19.6 mg/L for mycelial growth). Difenoconazole also inhibits growth of A. sonali, F. fulva, B. cinerea, and R. solani (EC50s = 0.131 mg/L, 0.069 mg/L, 0.297 mg/L, and 0.252 mg/L, respectively). |
| Name | difenoconazole |
|---|---|
| Synonym | More Synonyms |
| Description | Difenoconazole is a broad-spectrum triazole fungicide that inhibits ergosterol biosynthesis via inhibition of the cytochrome P450-dependent 14α-demethylation of lanosterol, which results in disruption of the fungal cell membrane and cell death. Difenoconazole inhibits the growth of F. graminearum isolates in vitro (EC50s = 1.69-19.6 mg/L for mycelial growth). Difenoconazole also inhibits growth of A. sonali, F. fulva, B. cinerea, and R. solani (EC50s = 0.131 mg/L, 0.069 mg/L, 0.297 mg/L, and 0.252 mg/L, respectively). |
|---|---|
| Related Catalog |
| Density | 1.4±0.1 g/cm3 |
|---|---|
| Boiling Point | 547.0±60.0 °C at 760 mmHg |
| Melting Point | 76°C |
| Molecular Formula | C19H17Cl2N3O3 |
| Molecular Weight | 406.263 |
| Flash Point | 284.6±32.9 °C |
| Exact Mass | 405.064697 |
| PSA | 58.40000 |
| LogP | 4.92 |
| Vapour Pressure | 0.0±1.5 mmHg at 25°C |
| Index of Refraction | 1.642 |
| InChIKey | BQYJATMQXGBDHF-UHFFFAOYSA-N |
| SMILES | CC1COC(Cn2cncn2)(c2ccc(Oc3ccc(Cl)cc3)cc2Cl)O1 |
| Storage condition | 0-6°C |
| Water Solubility | 3.3 mg/L (20 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Symbol |
GHS07, GHS09 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 + H332-H410 |
| Precautionary Statements | P273-P501 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
| Hazard Codes | Xn:Harmful |
| Risk Phrases | R22;R41;R43 |
| Safety Phrases | S26-S36/37/39 |
| RIDADR | UN 3077 9 / PGIII |
| RTECS | XZ4380000 |
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Comparison of greenhouse and field degradation behaviour of isoprocarb, hexaflumuron and difenoconazole in Perilla frutescens.
Bull. Environ. Contam. Toxicol. 89(4) , 868-72, (2012) Isoprocarb, hexaflumuron and difenoconazole were used in Perilla frutescens at 600, 60 and 75 g a.i./ha respectively. High performance liquid chromatography-tandem mass spectrometry was used for resid... |
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[Behaviour azole fungicide and fluconazole in Cryptococcus neoformans clinical and environmental isolates].
Rev. Soc. Bras. Med. Trop. 40(2) , 209-11, (2007) The activity of azole fungicides for agronomical use (epoxiconazole, difenoconazole and cyproconazole) was evaluated in comparison with the therapeutic antifungal agent fluconazole, on 23 environmenta... |
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Triazole fungicides can induce cross-resistance to medical triazoles in Aspergillus fumigatus.
PLoS ONE 7(3) , e31801, (2012) Azoles play an important role in the management of Aspergillus diseases. Azole resistance is an emerging global problem in Aspergillus fumigatus, and may develop through patient therapy. In addition, ... |
| Diflubenzuron |
| 2RS,4SR)-4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl]phenyl 4-chlorophenyl ether |
| 1-((2-[2-Chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl)methyl)-1H-1,2,4-triazole |
| 1-[2-[4-(4-Chlorophenoxy)-2-chlorophenyl]-4-methyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole |
| 3-chloro-4-[(2RS,4RS |
| 1-((2-(2-Chloro-4-(4-chlorophenoxy)phenyl)-4-methyl-1,3-dioxolan-2-yl)methyl)-1H-1,2,4-triazole |
| cis-trans-3-Chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl]phenyl 4-chlorophenyl ether |
| T5O COTJ BR BG DOR DG&& D1 B1- AT5NN DNJ |
| Difenoconazol |
| MFCD00144119 |
| 1-({2-[(2Ξ,4Ξ)-2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole |
| 1-({2-[2-Chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole |
| difenoconazole |
| 1-[[2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl]methyl]-1H-1,2,4-triazole |
| 1-[[2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl]methyl]-1,2,4-triazole |
| 1H-1,2,4-Triazole, 1-[[2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl]methyl]- |