DD283322A5 - Verfahren zur beeinflussung des pflanzenwachstums und mittel dazu - Google Patents

Verfahren zur beeinflussung des pflanzenwachstums und mittel dazu Download PDF

Info

Publication number: DD283322A5
Authority: DD; German Democratic Republic
Prior art keywords: ice; phenyl; chlorophenyl; fluorophenyl; dichlorophenyl
Prior art date: 1987-11-07

Application number

DD88321477A

Other languages

German (de)

English (en)

Inventor

Stefan Karbach

Bernd Janssen

Hans-Gert Recker

Hubert Smuda

Norbert Meyer

Johann Jung

Wilhelm Rademacher

Original Assignee

��@��k��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1987-11-07

Filing date

1988-11-04

Publication date

1990-10-10

1988-11-04 Application filed by ��@��k�� filed Critical ��@��k��

1990-10-10 Publication of DD283322A5 publication Critical patent/DD283322A5/de

Links

238000000034 method Methods 0.000 title claims description 13
230000008635 plant growth Effects 0.000 title claims description 10
230000008569 process Effects 0.000 title claims description 3
-1 2-trifluoromethylphenyl Chemical group 0.000 claims description 168
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 43
229910052736 halogen Inorganic materials 0.000 claims description 19
239000000203 mixture Substances 0.000 claims description 19
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 17
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 16
ZFOWEXGOKLKOFQ-UHFFFAOYSA-N 2-(oxiran-2-ylmethyl)-1h-pyrrole Chemical compound C=1C=CNC=1CC1CO1 ZFOWEXGOKLKOFQ-UHFFFAOYSA-N 0.000 claims description 15
229910052757 nitrogen Inorganic materials 0.000 claims description 12
239000002689 soil Substances 0.000 claims description 12
150000003839 salts Chemical class 0.000 claims description 11
239000004305 biphenyl Substances 0.000 claims description 10
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 9
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 9
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 8
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 7
229910052751 metal Inorganic materials 0.000 claims description 7
239000002184 metal Substances 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
235000010290 biphenyl Nutrition 0.000 claims description 5
125000006267 biphenyl group Chemical group 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 5
125000001624 naphthyl group Chemical group 0.000 claims description 5
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 5
150000003254 radicals Chemical class 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
239000007787 solid Substances 0.000 claims description 2
125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims 2
239000012050 conventional carrier Substances 0.000 claims 1
239000007788 liquid Substances 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 26
150000001875 compounds Chemical class 0.000 description 25
125000005843 halogen group Chemical group 0.000 description 14
239000004480 active ingredient Substances 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
239000000243 solution Substances 0.000 description 10
230000012010 growth Effects 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
229920005989 resin Polymers 0.000 description 8
239000011347 resin Substances 0.000 description 8
239000006185 dispersion Substances 0.000 description 7
238000002360 preparation method Methods 0.000 description 7
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 6
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000000126 substance Substances 0.000 description 6
229910021591 Copper(I) chloride Inorganic materials 0.000 description 5
235000013339 cereals Nutrition 0.000 description 5
OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 5
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229940079593 drug Drugs 0.000 description 5
239000000417 fungicide Substances 0.000 description 5
229910002027 silica gel Inorganic materials 0.000 description 5
239000000741 silica gel Substances 0.000 description 5
238000012360 testing method Methods 0.000 description 5
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
239000013543 active substance Substances 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
239000003630 growth substance Substances 0.000 description 4
159000000000 sodium salts Chemical class 0.000 description 4
239000002904 solvent Substances 0.000 description 4
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229940126062 Compound A Drugs 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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240000005979 Hordeum vulgare Species 0.000 description 3
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MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
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238000006243 chemical reaction Methods 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000011161 development Methods 0.000 description 3
230000018109 developmental process Effects 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
125000001188 haloalkyl group Chemical group 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000002480 mineral oil Substances 0.000 description 3
235000010446 mineral oil Nutrition 0.000 description 3
230000009467 reduction Effects 0.000 description 3
230000002829 reductive effect Effects 0.000 description 3
229910052725 zinc Inorganic materials 0.000 description 3
239000011701 zinc Substances 0.000 description 3
ODNQBVKKRIYVEP-UHFFFAOYSA-N 2-(bromomethyl)-3-(2-chlorophenyl)-2-phenyloxirane Chemical compound ClC1=CC=CC=C1C1C(C=2C=CC=CC=2)(CBr)O1 ODNQBVKKRIYVEP-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 2
235000006008 Brassica napus var napus Nutrition 0.000 description 2
240000000385 Brassica napus var. napus Species 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
235000010469 Glycine max Nutrition 0.000 description 2
235000003222 Helianthus annuus Nutrition 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
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240000007594 Oryza sativa Species 0.000 description 2
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229910019142 PO4 Inorganic materials 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
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PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
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229920001807 Urea-formaldehyde Polymers 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
150000001450 anions Chemical class 0.000 description 2
SMLHHBQGIJMAIM-UHFFFAOYSA-N calcium;2-dodecylbenzenesulfonic acid Chemical compound [Ca].CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O SMLHHBQGIJMAIM-UHFFFAOYSA-N 0.000 description 2
TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 2
239000000969 carrier Substances 0.000 description 2
235000020971 citrus fruits Nutrition 0.000 description 2
238000004440 column chromatography Methods 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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235000013399 edible fruits Nutrition 0.000 description 2
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230000005764 inhibitory process Effects 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000002844 melting Methods 0.000 description 2
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238000000926 separation method Methods 0.000 description 2
238000004904 shortening Methods 0.000 description 2
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235000011152 sodium sulphate Nutrition 0.000 description 2
238000009331 sowing Methods 0.000 description 2
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JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
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JSJJUPLUXJZYSA-UHFFFAOYSA-N 1-(3-bromo-2-phenylprop-1-enyl)-2-chlorobenzene Chemical compound ClC1=CC=CC=C1C=C(CBr)C1=CC=CC=C1 JSJJUPLUXJZYSA-UHFFFAOYSA-N 0.000 description 1
WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 1
MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 description 1
YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 1
125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 description 1
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YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
UPTVJAJPBGIRLZ-UHFFFAOYSA-N 2-(trichloromethylsulfanyl)-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical compound C1CC=CC2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C21 UPTVJAJPBGIRLZ-UHFFFAOYSA-N 0.000 description 1
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BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
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NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 1
CDIJOYCNNFLOAX-UHFFFAOYSA-N 4-(trichloromethylsulfanyl)isoindole-1,3-dione Chemical compound ClC(Cl)(Cl)SC1=CC=CC2=C1C(=O)NC2=O CDIJOYCNNFLOAX-UHFFFAOYSA-N 0.000 description 1
NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
239000005725 8-Hydroxyquinoline Substances 0.000 description 1
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241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
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244000025254 Cannabis sativa Species 0.000 description 1
REEFSLKDEDEWAO-UHFFFAOYSA-N Chloraniformethan Chemical compound ClC1=CC=C(NC(NC=O)C(Cl)(Cl)Cl)C=C1Cl REEFSLKDEDEWAO-UHFFFAOYSA-N 0.000 description 1
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YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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PUPBZBNNTFBFDS-UHFFFAOYSA-N n-cyclohexyl-2,4,5-trimethylfuran-3-carboxamide Chemical compound CC1=C(C)OC(C)=C1C(=O)NC1CCCCC1 PUPBZBNNTFBFDS-UHFFFAOYSA-N 0.000 description 1
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150000003460 sulfonic acids Chemical class 0.000 description 1
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239000011593 sulfur Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
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239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 description 1
239000011135 tin Substances 0.000 description 1
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150000003738 xylenes Chemical class 0.000 description 1
MAZZTUAWFTWGKB-UHFFFAOYSA-L zinc ethane-1,2-diamine manganese(2+) dicarbamodithioate Chemical compound [Mn+2].[Zn+2].NCCN.NC([S-])=S.NC([S-])=S MAZZTUAWFTWGKB-UHFFFAOYSA-L 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Environmental Sciences (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Health & Medical Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Luminescent Compositions (AREA)
Pyrrole Compounds (AREA)
Polyesters Or Polycarbonates (AREA)
Epoxy Compounds (AREA)
Cultivation Of Plants (AREA)

DD88321477A 1987-11-07 1988-11-04 Verfahren zur beeinflussung des pflanzenwachstums und mittel dazu DD283322A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19873737888 DE3737888A1 (de)	1987-11-07	1987-11-07	Verfahren zur beeinflussung des pflanzenwachstums durch azolylmethyloxirane

Publications (1)

Publication Number	Publication Date
DD283322A5 true DD283322A5 (de)	1990-10-10

Family

ID=6340039

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD88321477A DD283322A5 (de)	1987-11-07	1988-11-04	Verfahren zur beeinflussung des pflanzenwachstums und mittel dazu

Country Status (9)

Country	Link
EP (1)	EP0315850B1 (fr)
JP (1)	JP2765878B2 (fr)
KR (1)	KR960007690B1 (fr)
AT (1)	ATE78131T1 (fr)
CA (1)	CA1329995C (fr)
DD (1)	DD283322A5 (fr)
DE (2)	DE3737888A1 (fr)
FI (1)	FI89854C (fr)
HU (1)	HU203832B (fr)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3907729A1 (de) *	1989-03-10	1990-09-13	Basf Ag	Trifluormethylphenylazolylmethyloxirane, verfahren zu ihrer herstellung und deren verwendung als pflanzenschutzmittel
DE59000731D1 (de) *	1989-03-21	1993-02-25	Basf Ag	Herbizide und pflanzenwachstumsregulierende azolylmethyloxirane.
DE3936824A1 (de) *	1989-11-04	1991-05-08	Basf Ag	N-oxo-azolylmethyloxirane und diese enthaltende fungizide und bioregulatoren
GB9116672D0 (en) *	1991-08-01	1991-09-18	Hickson Int Plc	Preservatives for wood and other cellulosic materials
WO1993002557A1 (fr) *	1991-08-01	1993-02-18	Hickson International Plc	Agents de conservation pour le bois et autres materiaux cellulosiques
PL195763B1 (pl)	1997-06-30	2007-10-31	Monsanto Technology Llc	Kompozycja do kontrolowanego uwalniania zapewniająca środek grzybobójczy roślinie i sposób wytwarzania kompozycji
MXPA04011458A (es)	2002-06-24	2005-02-14	Basf Ag	Procedimiento para la obtencion de 1, 2, 4-triazolilmetil-oxiranos.
WO2005056548A1 (fr) *	2003-12-11	2005-06-23	Cheminova A/S	Epoxiconazole enantiomeriquement pur et ses utilisations en tant qu'agent phytosanitaire
WO2006059759A1 (fr) *	2004-11-30	2006-06-08	Sumitomo Chemical Company, Limited	Procede de production d’un derive epoxytriazole
PL1933623T3 (pl) *	2005-10-07	2010-02-26	Basf Se	Mieszaniny grzybobójcze i bioregulujące
WO2007088116A2 (fr) *	2006-01-31	2007-08-09	Basf Se	Mélanges fongicides contenant de l'époxiconazole et du metiram
CN101472918A (zh) *	2006-06-21	2009-07-01	巴斯夫欧洲公司	唑基甲基环氧乙烷及其在防治植物病原性真菌中的用途和包含它们的组合物
BRPI0713131A2 (pt) *	2006-06-23	2012-04-17	Basf Se	compostos, uso de compostos, composição para a proteção de colheitas, semente, e, processo para combater fungos fitopatogênicos
ATE495170T1 (de) *	2006-06-23	2011-01-15	Basf Se	Azolylmethyloxirane, ihre verwendung zur bekämpfung von pflanzenpathogenen pilzen sowie sie enthaltende mittel
DE502007002119D1 (de) *	2006-07-05	2010-01-07	Basf Se	Azolylmethyloxirane, ihre verwendung zur bekämpfung von pflanzenpathogenen pilzen sowie sie enthaltende mittel
WO2008003607A1 (fr) *	2006-07-05	2008-01-10	Basf Se	Azolylméthyloxyranes, leur utilisation pour lutter contre des champignons phytopathogènes et agents les contenant
EP2046780A1 (fr) *	2006-07-24	2009-04-15	Basf Se	Azolylméthyloxiranes, leur utilisation dans la lutte contre des champignons phytopathogènes et agents les contenant
US7910614B2 (en) *	2006-07-25	2011-03-22	Basf Se	Azolylmethyloxiranes, use thereof for controlling plant pathogenic fungi, and agents containing the same
EP2234488A2 (fr) *	2007-12-19	2010-10-06	Basf Se	Azolylméthyloxiranes, leur utilisation et agents les contenant
EP2235005A2 (fr) *	2007-12-19	2010-10-06	Basf Se	Azolylméthyloxiranes, leur utilisation et agents les contenant
JP2011507815A (ja) *	2007-12-19	2011-03-10	ビーエーエスエフソシエタス・ヨーロピア	アゾリルメチルオキシラン類、それらの使用およびそれらを含む組成物
EP2746275A1 (fr)	2012-12-19	2014-06-25	Basf Se	Nouveaux triazoles substitués et imidazoles et leur utilisation comme fongicides
EP2746277A1 (fr)	2012-12-19	2014-06-25	Basf Se	Composés triazolyles et imidazolyles fongicides
WO2014095555A1 (fr)	2012-12-19	2014-06-26	Basf Se	Nouveaux triazoles et imidazoles substitués et leur utilisation en tant que fongicides
EP2746276A1 (fr)	2012-12-19	2014-06-25	Basf Se	Nouveaux triazoles substitués et imidazoles et leur utilisation comme fongicides
CA3038401A1 (fr)	2016-09-29	2018-04-05	Bayer Cropscience Aktiengesellschaft	Derives d'imidazolylmethyloxirane a substitution en position 5 en tant que fongicides

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3111238A1 (de) *	1981-03-21	1982-10-07	Bayer Ag, 5090 Leverkusen	Substituierte triazolylmethyl-oxirane, verfahren zu ihrer herstellung sowie ihre verwendung als zwischenprodukte
IL68433A (en) *	1982-05-14	1986-04-29	Basf Ag	Azolylmethyloxiranes,their manufacture and their use as fungicides and in pharmaceutical compositions
DE3537817A1 (de) *	1985-10-24	1987-04-30	Bayer Ag	Verfahren zur herstellung von oxiranen

1987
- 1987-11-07 DE DE19873737888 patent/DE3737888A1/de not_active Withdrawn
1988
- 1988-10-31 EP EP88118076A patent/EP0315850B1/fr not_active Expired - Lifetime
- 1988-10-31 AT AT88118076T patent/ATE78131T1/de not_active IP Right Cessation
- 1988-10-31 DE DE8888118076T patent/DE3872831D1/de not_active Expired - Lifetime
- 1988-11-04 CA CA000582228A patent/CA1329995C/fr not_active Expired - Fee Related
- 1988-11-04 DD DD88321477A patent/DD283322A5/de unknown
- 1988-11-04 FI FI885097A patent/FI89854C/fi not_active IP Right Cessation
- 1988-11-04 HU HU885709A patent/HU203832B/hu not_active IP Right Cessation
- 1988-11-07 KR KR1019880014638A patent/KR960007690B1/ko not_active Expired - Fee Related
- 1988-11-07 JP JP63279549A patent/JP2765878B2/ja not_active Expired - Fee Related

Also Published As

Publication number	Publication date
EP0315850A3 (en)	1990-01-24
FI885097A0 (fi)	1988-11-04
KR890007641A (ko)	1989-07-05
JP2765878B2 (ja)	1998-06-18
HU203832B (en)	1991-10-28
DE3872831D1 (de)	1992-08-20
DE3737888A1 (de)	1989-05-18
ATE78131T1 (de)	1992-08-15
FI885097L (fi)	1989-05-08
HUT49460A (en)	1989-10-30
FI89854B (fi)	1993-08-31
EP0315850A2 (fr)	1989-05-17
JPH01157905A (ja)	1989-06-21
KR960007690B1 (ko)	1996-06-08
FI89854C (fi)	1993-12-10
EP0315850B1 (fr)	1992-07-15
CA1329995C (fr)	1994-06-07

Publication	Publication Date	Title
EP0315850B1 (fr)	1992-07-15	Procédé pour influencer la croissance des plantes par des azolylméthyloxiranes
DD158845A5 (de)	1983-02-09	Pflanzenbehandlungsmittel
EP0433780B1 (fr)	1996-04-03	Azolylméthylcycloalkanols substitués et fongicides les contenant
EP0097881A2 (fr)	1984-01-11	Azolyl-cétones et -alcools substitués
EP0017209B1 (fr)	1982-12-22	Sels d'alcoylammonium substitués, leur préparation et leur utilisation pour la régulation de la croissance des plantes
DE2845254A1 (de)	1980-05-08	Gamma -azolylverbindungen
EP0031911A2 (fr)	1981-07-15	Triazolylméthyl-tert.-butyl-cétones substituées, procédé pour leur préparation ainsi que leur utilisation comme agents protecteurs des plantes et comme intermédiaires
DE3909862A1 (de)	1990-09-27	Azolylethylcyclopropane, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel
EP0229642B1 (fr)	1990-07-11	Dérivés d'azoles, fongicides et régulateur de croissance les contenant
EP0095677B1 (fr)	1986-06-18	Triazolyl-cétonoximes et dioximes, leur procédé de préparation et leur application comme agents régulateurs de croissance des plantes
EP0363766B1 (fr)	1991-04-10	Azolylméthylcyclopropanes et leur application comme produits protecteurs pour plantes
EP0092730A2 (fr)	1983-11-02	Dérivés bis azolyls, leur préparation, leur application comme agents régulateurs de croissance des plantes et les compositions les contenant
EP0270002B1 (fr)	1992-04-15	Dérivés de cyclohexénone
DE3941593A1 (de)	1991-06-20	Azolylmethylcycloalkanole
EP0421227B1 (fr)	1994-06-15	Dérivés du 1-hydroxy-1,2,4-triazole et fongicides les contenant et agents régulateurs de croissance
EP0076446A2 (fr)	1983-04-13	Azolylalkyl-2,3-dihydrobenzofuranes ayant une action de régulateurs de croissance des plantes et leur application
DE3604871A1 (de)	1987-08-20	Cyclohexenonderivate, verfahren zu ihrer herstellung und ihre verwendung als mittel zur regulierung des pflanzenwachstums
EP0394843B1 (fr)	1993-12-15	Halovinyl-azoles et fungicides et régulateurs de croissance des plantes les contenant
EP0230268A2 (fr)	1987-07-29	Composé d'azole halogénés et fungicides les contenant
DE3523862A1 (de)	1987-01-08	Mittel zur regulierung des pflanzenwachstums
EP0076445B1 (fr)	1985-05-29	Agent de régulation de croissance des plantes
EP0407877B1 (fr)	1994-06-29	Dérivés de 1,2-dihalo-azolyléthane et fongicides les contenant
DE3435944A1 (de)	1986-04-10	Vinyl-carbamoyl-imidazole enthaltende mittel zur regulierung des pflanzenwachstums
DE3914944A1 (de)	1990-11-08	Azolylethanderivate und diese enthaltende fungizide und wachstumsregulatoren
DE3932387A1 (de)	1991-04-11	Vinylazole und ihre verwendung als pflanzenschutzmittel