Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H20N2O3 |
| Molecular Weight | 300.3523 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1NNC(=O)OC(C)C)C2=CC=CC=C2
InChI
InChIKey=VHLKTXFWDRXILV-UHFFFAOYSA-N
InChI=1S/C17H20N2O3/c1-12(2)22-17(20)19-18-15-11-14(9-10-16(15)21-3)13-7-5-4-6-8-13/h4-12,18H,1-3H3,(H,19,20)
| Molecular Formula | C17H20N2O3 |
| Molecular Weight | 300.3523 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Genetic analysis and cross-resistance spectrum of a laboratory-selected chlorfenapyr resistant strain of two-spotted spider mite (Acari: Tetranychidae). | 2004 |
|
| Side effects of five new acaricides on the predator Galendromus occidentalis (Acari, Phytoseiidae). | 2006 |
|
| Toxicity of bifenazate and its principal active metabolite, diazene, to Tetranychus urticae and Panonychus citri and their relative toxicity to the predaceous mites, Phytoseiulus persimilis and Neoseiulus californicus. | 2007 |
|
| Organophosphate insecticides and acaricides antagonise bifenazate toxicity through esterase inhibition in Tetranychus urticae. | 2007 Dec |
|
| A modified excised leaf disc method to estimate the toxicity of slow- and fast-acting reduced-risk acaricides to mites. | 2009 Dec |
|
| Acaricide resistance mechanisms in the two-spotted spider mite Tetranychus urticae and other important Acari: a review. | 2010 Aug |
|
| Compatibility of traditional and novel acaricides with bumblebees (Bombus terrestris): a first laboratory assessment of toxicity and sublethal effects. | 2010 Jul |
|
| The complete mitochondrial genome of the citrus red mite Panonychus citri (Acari: Tetranychidae): high genome rearrangement and extremely truncated tRNAs. | 2010 Oct 23 |
|
| A novel action of highly specific acaricide; bifenazate as a synergist for a GABA-gated chloride channel of Tetranychus urticae [Acari: Tetranychidae]. | 2012 Jun |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:35:43 GMT 2023
by
admin
on
Fri Dec 15 18:35:43 GMT 2023
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| Record UNII |
24Z9QW0505
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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EPA PESTICIDE CODE |
586
Created by
admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
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| Code System | Code | Type | Description | ||
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176879
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DTXSID5032525
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C508134
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m2481
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PRIMARY | Merck Index | ||
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149877-41-8
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24Z9QW0505
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bifenazate
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7002
Created by
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PRIMARY |