Name | Benzene, 1-((2-(4-chlorophenyl)-2-methylpropoxy)methyl)-3-phenoxy- |
Synonyms | MTI 501 Chloproxyfen chlorfenprox Chlorfenprox Ethopermethrin 3-Phenoxybenzyl 2-(4-chlorophenyl)-2-methylpropyl ether 2-(4-chlorophenyl)-2-methylpropyl-3-phenoxybenzyl ether 3-Phenoxybenzyl [2-methyl-2-(p-chlorophenyl)]propyl ether -((2-(4-Chlorophenyl)-2-methylpropoxy)methyl)-3-phenoxybenzene 1-{[2-(4-chlorophenyl)-2-methylpropoxy]methyl}-3-phenoxybenzene 1-((2-(4-CHLOROPHENYL)-2-METHYLPROPOXY)METHYL)-3-PHENOXYBENZENE Benzene, 1-((2-(4-chlorophenyl)-2-methylpropoxy)methyl)-3-phenoxy- |
CAS | 80844-01-5 |
InChI | InChI=1/C23H23ClO2/c1-23(2,19-11-13-20(24)14-12-19)17-25-16-18-7-6-10-22(15-18)26-21-8-4-3-5-9-21/h3-15H,16-17H2,1-2H3 |
Molecular Formula | C23H23ClO2 |
Molar Mass | 366.88 |
Density | 1.138±0.06 g/cm3(Predicted) |
Boling Point | 458.0±35.0 °C(Predicted) |
Flash Point | 129.3°C |
Vapor Presure | 3.87E-08mmHg at 25°C |
Storage Condition | 2-8°C |
Refractive Index | 1.577 |
Physical and Chemical Properties | Appearance is colorless transparent liquid, B. p.205 ~ 207 ℃/20Pa,80 ℃ 3 months without obvious decomposition, stable at room temperature for more than 1 month under light conditions. |
Use | a broad-spectrum pyrethroid insecticide. For the prevention and control of cotton bollworm, tobacco armyworm, cotton pink bollworm, Cotton leaf wave moth, Spodoptera exigua, subtropical armyworm, Cotton leaf roller Borer, aphids, pod bug, greenhouse whitefly, Mexico cotton bollworm, dosage 0.9~2g/100; For the prevention and control of diamondback moth, a star armyworm, armyworm, peach aphid and other vegetable pests, dosage 0.98~2g/100; For the prevention and control of corn borer, Borer, corn aphids, dosage 0.75~1.5g/100. In addition, it cannot be used to control various pests on tobacco, soybean, potato, rice and fruit trees. The mites also have a certain ability to kill. |
production method | preparation method-preparation of tert-butyl chloride tert-butyl alcohol is reacted with hydrochloric acid, mixed and shaken for 20min. Preparation of 2-(4-chlorophenyl)-2-methylpropane in a mixture of chlorobenzene and anhydrous ferric chloride, dry hydrogen chloride is added, and tert-butyl chloride is added dropwise at 30 °c, the reaction was continued for 2H after instillation. Preparation of 2-(4-chlorophenyl)-2-chloromethylpropane the product of the previous step was reacted with thionyl chloride in the presence of the catalyst benzoyl peroxide for 2H at 100 °c. Synthesis of permethrin the product of the previous step was reacted with M-phenoxybenzyl alcohol and sodium hydroxide in a solvent with nitrogen gas and stirred at 120 ° C. For 8 hours. Preparation Method 2 preparation method 3 |