240494-70-6

Usage

Uses

Since the provided materials do not specify the exact applications of [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl 2,2-dimethyl-3-pro p-1-enyl-cyclopropane-1-carboxylate, it is not possible to list its uses based on the given information. However, given its complex structure, it is likely to have specialized applications in fields such as pharmaceuticals, materials science, or chemical research. Further context or analysis would be required to determine its specific uses.

InChI:InChI=1/C18H20F4O3/c1-5-6-11-12(18(11,2)3)17(23)25-8-10-15(21)13(19)9(7-24-4)14(20)16(10)22/h5-6,11-12H,7-8H2,1-4H3

Synthetic route

2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl alcohol (83282-91-1) + 2,2-dimethyl-3-(1-propenyl) cyclopropane methyl carboxylate (40447-55-0) → metofluthrin (240494-70-6)

Conditions	Yield
With lithium methanolate In n-heptane at 95 - 105℃; for 16h; Product distribution / selectivity; Heating / reflux;
With lithium methanolate In n-heptane at 95 - 105℃; for 17h; Product distribution / selectivity; Heating / reflux;

Upstream product

• 83282-91-1 2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl alcohol 
• 40447-55-0 2,2-dimethyl-3-(1-propenyl) cyclopropane methyl carboxylate 

Relevant academic research and scientific papers

METHOD FOR MANUFACTURING PURIFIED BENZYL ESTER COMPOUND

PROBLEM TO BE SOLVED: To provide a method for mass-productively manufacturing a benzyl ester compound in an industrial scale which permits the manufacture of a purified cyclopropanecarboxylic acid benzyl ester compound of high purity in an excellent yield with reduced energy consumption. SOLUTION: The method for manufacturing the purified ester compound comprises steam-distilling, using a distillation apparatus equipped with a rectification column, a crude product containing the cyclopropanecarboxylic acid benzyl ester compound obtained by a transesterification reaction of a cyclopropanecarboxylic acid ester compound with a benzyl alcohol compound.

Insecticide transpiration apparatus

There is provided an insecticide transpiration apparatus capable of transpiring insecticide at room temperature. The apparatus includes an apparatus main body having a recipient recess capable of accommodating an insecticide cartridge, an insecticide cartridge rotatably supported in the recipient recess, a driving means which is composed of a motor connected to a rotation support shaft of the insecticide cartridge and an electric source and which is contained in the apparatus main body, and a cover pivoted to the apparatus main body so as to cover the insecticide cartridge in the recipient recess, wherein the insecticide cartridge includes an annular hollow structure which accommodates granular insecticide-impregnated bodies and which has openings in an inner peripheral surface and an outer peripheral surface thereof, a core portion situated at the center of the hollow structure and connected to the rotation support shaft, a plurality of spoke portions connecting the core portion and the hollow structure, and blade portions integrally formed with the hollow structure so as to extend from the inner peripheral surface toward the center thereof and adapted to promote passing of air from the inner peripheral surface to the outer peripheral surface of the hollow structure.