DD256637A5

DD256637A5 - Herbizide zusammensetzung

Herbizide zusammensetzung Download PDF

Info

Publication number: DD256637A5
Authority: DD; German Democratic Republic
Prior art keywords: group; chloro; trifluoromethylphenoxy; nitro; carbon atoms
Prior art date: 1985-06-10

Application number

DD29116586A

Other languages

German (de)

English (en)

Inventor

Yoshiharu Hayashi

Teruyuki Misumi

Original Assignee

Asahi Kasei Kogyo Kabushiki Kaisha,Jp

Priority date

1985-06-10

Filing date

1986-06-10

Publication date

1988-05-18

1986-06-10 Application filed by Asahi Kasei Kogyo Kabushiki Kaisha,Jp filed Critical Asahi Kasei Kogyo Kabushiki Kaisha,Jp

1988-05-18 Publication of DD256637A5 publication Critical patent/DD256637A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 79
239000000203 mixture Substances 0.000 title claims abstract description 61
150000001875 compounds Chemical class 0.000 claims abstract description 142
238000000034 method Methods 0.000 claims abstract description 51
241000196324 Embryophyta Species 0.000 claims abstract description 47
239000004480 active ingredient Substances 0.000 claims abstract description 15
230000006378 damage Effects 0.000 claims abstract description 7
-1 2-chloro-4-trifluoromethylphenoxy Chemical group 0.000 claims description 145
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 81
125000004432 carbon atom Chemical group C* 0.000 claims description 78
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 50
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 38
125000000217 alkyl group Chemical group 0.000 claims description 36
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 33
239000000460 chlorine Substances 0.000 claims description 25
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 25
125000004430 oxygen atom Chemical group O* 0.000 claims description 21
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 19
239000002253 acid Substances 0.000 claims description 17
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 15
125000003545 alkoxy group Chemical group 0.000 claims description 12
KXKVLQRXCPHEJC-UHFFFAOYSA-N methyl acetate Chemical compound COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 9
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150000001340 alkali metals Chemical class 0.000 claims description 8
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125000000304 alkynyl group Chemical group 0.000 claims description 8
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DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 7
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KOUKXHPPRFNWPP-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid;hydrate Chemical compound O.OC(=O)C1=CN=C(C(O)=O)C=N1 KOUKXHPPRFNWPP-UHFFFAOYSA-N 0.000 claims description 5
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IPBVNPXQWQGGJP-UHFFFAOYSA-N phenyl acetate Chemical compound CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 claims description 3
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IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
229910052801 chlorine Chemical group 0.000 claims 4
159000000001 potassium salts Chemical class 0.000 claims 4
125000000547 substituted alkyl group Chemical group 0.000 claims 4
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229910052799 carbon Inorganic materials 0.000 claims 1
PIQOWNMGSYZITA-UHFFFAOYSA-N ethyl 2-[2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenyl]-2-oxoethoxy]acetate Chemical compound C1=C([N+]([O-])=O)C(C(=O)COCC(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 PIQOWNMGSYZITA-UHFFFAOYSA-N 0.000 claims 1
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150000004702 methyl esters Chemical class 0.000 claims 1
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239000000126 substance Substances 0.000 abstract description 30
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238000006243 chemical reaction Methods 0.000 description 39
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NYBWUHOMYZZKOR-UHFFFAOYSA-N tes-adt Chemical class C1=C2C(C#C[Si](CC)(CC)CC)=C(C=C3C(SC=C3)=C3)C3=C(C#C[Si](CC)(CC)CC)C2=CC2=C1SC=C2 NYBWUHOMYZZKOR-UHFFFAOYSA-N 0.000 description 25
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238000002360 preparation method Methods 0.000 description 20
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 19
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150000002923 oximes Chemical class 0.000 description 14
240000008042 Zea mays Species 0.000 description 13
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WTDHULULXKLSOZ-UHFFFAOYSA-N hydroxylamine hydrochloride Substances Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 13
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ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
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235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 11
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QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
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IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
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WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 4
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ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
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150000007524 organic acids Chemical class 0.000 description 3
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230000000704 physical effect Effects 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
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239000004323 potassium nitrate Substances 0.000 description 3
235000010333 potassium nitrate Nutrition 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
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125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 2
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VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
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