Abstract:
PURPOSE: A chelate resin for adsorbing specific heavy metal ions and its preparation method are provided, to improve the adsorbing property to specific heavy metal ions by introducing a dithiocarbamic acid group into the main chain and the side chain of a polymer and employing the benzene structure as a spacer, thereby allowing the neighboring dithiocarbamic acid groups to form zigzag structure. CONSTITUTION: The chelate resin is represented by the formula 1, wherein A is H, K or Na. The method comprises the steps of preparing a spherical copolymer represented by the formula 2 by suspension polymerization of styrene and methyl methacrylate using a divinylbenzene as a crosslinking agent; reacting the copolymer of the formula 2 with boron hydride, zinc chloride and N,N'-dimethylaniline to convert a carboxyl ester group into a hydroxymethyl group (-CH2OH), and reacting the obtained one with pyridine and thionyl chloride to convert the hydroxymethyl group into a chloromethyl group and to prepare the chloromethyl group-containing copolymer represented by the formula 3; reacting the copolymer of the formula 3 with zinc chloride and chloromethyl methylether to introduce a chloromethyl group to a phenyl ring and to prepare the copolymer which contains two chloromethyl groups bonded to different positions and is represented by the formula 4; reacting the copolymer of the formula 4 with methyl amine to prepare the aminated copolymer represented by the formula 5; and reacting the copolymer of the formula 5 with carbon disulfide to introduce a dithiocarbamic acid group and neutralizing the obtained one.
Abstract:
PURPOSE: Provided are novel propanoic ester and amide derivatives having an oxime group as a branched chain, which are excellent in disinfecting activity, a preparation thereof, and a disinfectant composition containing the propanoic ester and amide derivatives. CONSTITUTION: The propaonic ester and amide derivatives represented by the formula 1 are produced by a process comprising the steps of: reacting a bromine compound represented by the formula 2 and 2,3-butanedione monoxime represented by the formula 3 in the presence of a base to produce an oxime-based ketone compound; reducing the oxime-based ketone compound or condensing the oxime-based ketone compound with a hydroxyl amine to produce an oxime-based alcohol compound or a dioxime-based compound; reacting the oxime-based alcohol compound or the dioxime-based compound with a propanyl fluoride compound in the presence of a base. In the formula, R1 is trifluoromethyl, R2 is a phenyl group, X is CH or N, and Y is O or NH.
Abstract:
PURPOSE: Provided is 5-benzyloxymethyl-1,2-isoxazoline derivative which has an excellent herbicidal activity. Also, provided are its manufacturing method and herbicides containing the derivative as an active ingredient. CONSTITUTION: 5-benzyloxymethyl-1,2-isoxazoline derivative is represented by the formula(I), wherein X1, X2 and X3 individually represent hydrogen, methyl group, ethyl group, halogen group, methoxy group or nitro group (provided that it is an exception that X1, X2 and X3 are decimals all together); Y1, Y2 and Y3 are individually hydrogen or fluorine.
Abstract:
The new compound as 5-(2H-1-benzopyran-6-yl)-2-[1-(ethoxylimino) butyryl -3-hydroxy cyclohex-2-en-1-one (I) is prepared by (1) reacting 4-hydroxy benzaldehyde and 4-propazyl halide to get 4-propazyl 2H- 1- benzypyran-6- carboxaldehyde (II), (2) reacting (II) in alkali to get 4- (2H-1-benzopyran -6-y l0-3-buten-2-one (III), (3) reacting (III) with diethyl malonate to get 5-(2H-1-benzopyran-6-yl)- cyclohexan-1,3-dione (IV), (4) reacting (IV) with butyrate to get 2-butyryl-5-(2H-1-benzopyran-6-yl) -3-hydroxy cyclohex-2-en-1-one (V), reacting (V) with ethoxyl amine and sodium acetate to get (I). (I) as herbicide is useful for soybean, cotton, sugarbeet, sunflower, strawberry, wheat, corn and rice.
Abstract:
The derivative of formula (I) is useful for herbicides or plant growth regulants. In (I), X is H, 1-6c alkyl, 2-6c alkoxy, halogen, 1-6c haloalkyl, NO2, CN, 1-6c alkylthio, 1-6c alkylsulphinyl, 1-6c alkylsulphonyl, sulphamoyl, N-(1-6c alkyl) sulphamoyl or N,N-di(1-6c alkyl) sulphamoyl; R1 is H or 1-4c alkyl; R2 is 1-6c alkyl, 2-6c alkenyl or 2-6c alkynyl; R3 is H, 1-6c alkyl, 1-6c haloalkyl, 2-6c alkenyl, 2-6c haloalkenyl, 2-6c alkoxyalkyl, 2-6c alkylthioakyl, benzyl or 2-6c haloalkanoyl; R4 is H, alkali metal cation, alkaline earth metal cation, 1-4c alkanoyl, 1-4c haloalkanoyl or benzoyl.