famoxadone structure
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Common Name | famoxadone | ||
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CAS Number | 131807-57-3 | Molecular Weight | 374.389 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 491.3±55.0 °C at 760 mmHg | |
Molecular Formula | C22H18N2O4 | Melting Point | 140.3-141.8ºC | |
MSDS | N/A | Flash Point | 250.9±31.5 °C | |
Symbol |
GHS02, GHS07 |
Signal Word | Danger |
Use of famoxadoneFamoxadone (DPX-JE874) is a fungicide acting against a broad spectrum of fungi and is widely used in Integrated Pest Management strategies in different agricultural crops[1]. |
Name | famoxadone |
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Synonym | More Synonyms |
Description | Famoxadone (DPX-JE874) is a fungicide acting against a broad spectrum of fungi and is widely used in Integrated Pest Management strategies in different agricultural crops[1]. |
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Related Catalog | |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 491.3±55.0 °C at 760 mmHg |
Melting Point | 140.3-141.8ºC |
Molecular Formula | C22H18N2O4 |
Molecular Weight | 374.389 |
Flash Point | 250.9±31.5 °C |
Exact Mass | 374.126648 |
PSA | 67.87000 |
LogP | 4.76 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.659 |
Storage condition | 0-6°C |
Symbol |
GHS02, GHS07 |
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Signal Word | Danger |
Hazard Statements | H225-H302-H312-H319-H332 |
Precautionary Statements | P210-P280-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xn,N,F |
Risk Phrases | R48/22 |
Safety Phrases | S46 |
RIDADR | UN1648 3/PG 2 |
Hazard Class | 9.0 |
~% famoxadone CAS#:131807-57-3 |
Literature: US5948805 A1, ; |
~% famoxadone CAS#:131807-57-3 |
Literature: Pest Management Science, , vol. 57, # 2 p. 143 - 152 |
Precursor 1 | |
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DownStream 0 |
Development and validation of one-step ultrasound-assisted extraction for simultaneous determination of multiclass fungicides in soils.
J. AOAC Int. 98(1) , 192-200, (2015) A rapid, efficient, and simple one-step ultrasound-assisted extraction (UAE) method was developed for the analysis of seven fungicides (cymoxanil, metalaxyl, mandipropamid, folpet, chlorothalonil, kre... |
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Triplet state of the semiquinone-Rieske cluster as an intermediate of electronic bifurcation catalyzed by cytochrome bc1.
Biochemistry 52 , 6388-95, (2013) Efficient energy conversion often requires stabilization of one-electron intermediates within catalytic sites of redox enzymes. While quinol oxidoreductases are known to stabilize semiquinones, one of... |
5-Methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione |
(RS)-3-anilino-5-methyl-5-(4-phenoxyphenyl)-1,3-oxazolidine-2,4-dione |
3-Anilino-5-methyl-5-(4-phenoxyphenyl)oxazolidine-2,4-dione |
MFCD03427409 |
rac-(5R)-3-anilino-5-methyl-5-(4-phenoxyphenyl)-1,3-oxazolidine-2,4-dione |
T5OVNV EHJ CMR& E1 ER DOR |
Famoxate |
2,4-Oxazolidinedione, 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)- |
DPX-JE 874 |
famoxadone |
3-Anilino-5-methyl-5-(4-phenoxyphenyl)-1,3-oxazolidine-2,4-dione |
5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-2,4-oxazolidinedione |
EINECS 200-835-2 |
Famoxadon |