Detail of > 134098-61-6
- CAS Number:
- 134098-61-6
- Name:
Benzoicacid,4-[[[(E)-[(1,3-dimethyl-5-phenoxy-1H-pyrazol-4-yl)methylene]amino]oxy]methyl]-,1,1-dimethylethyl ester
- Superlist Name:
- Fenpyroximate
- Formula:
- C24H27N3O4
- Molecular Structure:
![Molecular Structure of 134098-61-6 (Benzoicacid,4-[[[(E)-[(1,3-dimethyl-5-phenoxy-1H-pyrazol-4-yl)methylene]amino]oxy]methyl]-,1,1-dimethylethyl ester)](http://www.lookchem.com/300w\2011-5\1029a9af-1438-4eab-8e20-ede8a197402b.png)
- Synonyms:
- Benzoicacid,4-[[[[(1,3-dimethyl-5-phenoxy-1H-pyrazol-4-yl)methylene]amino]oxy]methyl]-,1,1-dimethylethyl ester, (E)-;(E)-Fenpyroximate;Acari;Acari (pesticide);Assault;Danitron;Fenpiroximate;Fenpyroxymate;FujiMite;Kendo;Kiron;NNI 850;Naja;Naja (pesticide);Ortus;Portal;(Z,E)-Fenpyroximate;2-Methyl-2-propanyl-4-[({[(E)-(1,3-dimethyl-5-phenoxy-1H-pyrazol-4-yl)methylen]amino}oxy)methyl]benzoat;HOE 555-02A;Acari;Danitron;
- Molecular Weight:
- 421.4889
- Density:
- 1.136 g/cm3
- Boiling Point:
- 546.215 °C at 760 mmHg
- Flash Point:
- 284.141 °C
- Appearance:
- White crystalline powder
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Reference
- Rapid hydrolysis pathway for a tertiary alcohol ester through intramolecular transesterification in rats
- Rapid hydrolysis pathway for a tertiary alcohol ester through intramolecular transesterification in rats. Motoba, Kazuhiko; Nishizawa, Hideo; Suzuki, Takashi; Hamaguchi, Hiroshi; Uchida, Matazaemon (Inst. Life Sci. Res., NIHON NOHYAKU Co., Ltd., Kawachinagano 586, Japan). Biosci., Biotechnol. 134098-61-6 and 141097-12-3 which are cas registry numbers are also used here., Biochem., 56(2), 366-7 (English) 1992. CODEN: BBBIEJ. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) The tert-Bu ester group in the acaricide fenpyroximate was easily hydrolyzed by a rat liver microsomal system. Apparently, the ester bond cleavage of fenpyroximate occurs mostly via hydroxylation and subsequent intramol. transesterification, rather than by direct enzymic hydrolysis. .
- A laboratory-based method to measure relative pesticide and spray oil efficacy against broad mite, Polyphagotarsonemus latus (Banks) (Acari: Tarsonemidae)
- A laboratory-based method to measure relative pesticide and spray oil efficacy against broad mite, Polyphagotarsonemus latus (Banks) (Acari: Tarsonemidae). Herron, Grant; Jiang, Laura; Spooner-Hart, Robert (NSW Agriculture, Biological and Chemical Research Institute, Rydalmere 2116, Australia). Experimental and Applied Acarology, 20(9), 495-502 (English) 1996 Chapman & Hall. CODEN: EAACEM. ISSN: 0168-8162. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) Six pesticides and two spray oils were tested against Polyphagotarsonemus latus. The chems. were evaluated under lab. condition using a described bioassay. The pesticide toxicities fell into three distinct groups, namely abamectin, conventional pesticides and oils. The relative pesticide toxicities at the LC50 level were abamectin 4.9 ′ 10-8 g/L, endosulfan 1.1 ′ 10-3 g/L, fenpyroximate 2.3 ′ 10-3 g/L, pyridaben 4.1 ′ 10-3 g/L, tebufenpyrad 4.4 ′ 10-3 g/L, dicofol 4.5 ′ 10-3 g/L, petroleum spray oil 3.Several substances with their cas registry numbers 134098-61-6 and 96489-71-3 may be metioned in this study.4 ′ 10-1 g/L and canola oil 4.1 ′ 10-1 g/L. The calcn. of the LC99.9 values allows for resistance monitoring in P. latus and the suggested discriminating concns. are abamectin 1.0 ′ 10-4 g/L; endosulfan, pyridaben and dicofol 1.0 ′ 10-1 g/L fenpyroximate and tebufenpyrad 5.0 ′ 10-1 g/L. .
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