DD147807A5 - Fungizide mittel - Google Patents

Fungizide mittel Download PDF

Info

Publication number: DD147807A5
Authority: DD; German Democratic Republic
Prior art keywords: parts; weight; alkyl; oil; halogen
Prior art date: 1978-12-18

Application number

DD79217705A

Other languages

German (de)

English (en)

Inventor

Karl Eicken

Peter Plath

Ernst-Heinrich Pommer

Original Assignee

Basf Ag

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.)

1978-12-18

Filing date

1979-12-14

Publication date

1981-04-22

1979-12-14 Application filed by Basf Ag filed Critical Basf Ag

1981-04-22 Publication of DD147807A5 publication Critical patent/DD147807A5/de

Links

239000000417 fungicide Substances 0.000 title abstract description 13
150000001912 cyanamides Chemical class 0.000 claims abstract description 9
239000000460 chlorine Substances 0.000 claims description 92
-1 C 1 -C 2 Chemical group 0.000 claims description 32
230000000855 fungicidal effect Effects 0.000 claims description 14
229910052736 halogen Chemical group 0.000 claims description 13
239000000203 mixture Substances 0.000 claims description 13
150000002367 halogens Chemical group 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 10
229910052757 nitrogen Inorganic materials 0.000 claims description 9
125000004093 cyano group Chemical group *C#N 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
239000007787 solid Substances 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
229910052794 bromium Inorganic materials 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
239000011737 fluorine Substances 0.000 claims description 4
229910052731 fluorine Inorganic materials 0.000 claims description 4
125000004430 oxygen atom Chemical group O* 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000000304 alkynyl group Chemical group 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
239000007788 liquid Substances 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract description 15
238000004519 manufacturing process Methods 0.000 abstract 1
238000000034 method Methods 0.000 abstract 1
239000003921 oil Substances 0.000 description 30
239000004480 active ingredient Substances 0.000 description 26
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
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 description 12
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
239000011734 sodium Substances 0.000 description 12
229910052708 sodium Inorganic materials 0.000 description 12
239000002904 solvent Substances 0.000 description 12
239000006185 dispersion Substances 0.000 description 11
239000000243 solution Substances 0.000 description 10
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
241000233866 Fungi Species 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
241000196324 Embryophyta Species 0.000 description 8
239000002253 acid Substances 0.000 description 7
159000000000 sodium salts Chemical class 0.000 description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 6
239000013543 active substance Substances 0.000 description 6
239000012071 phase Substances 0.000 description 6
239000011591 potassium Substances 0.000 description 6
229910052700 potassium Inorganic materials 0.000 description 6
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
239000000741 silica gel Substances 0.000 description 6
229910002027 silica gel Inorganic materials 0.000 description 6
XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
150000001340 alkali metals Chemical class 0.000 description 5
239000012074 organic phase Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical class C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 5
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
206010061217 Infestation Diseases 0.000 description 4
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
150000002431 hydrogen Chemical group 0.000 description 4
239000003444 phase transfer catalyst Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
238000005507 spraying Methods 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
240000004713 Pisum sativum Species 0.000 description 3
240000003768 Solanum lycopersicum Species 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
229910052784 alkaline earth metal Inorganic materials 0.000 description 3
150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
239000002361 compost Substances 0.000 description 3
239000003814 drug Substances 0.000 description 3
229940079593 drug Drugs 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
239000008187 granular material Substances 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
238000002156 mixing Methods 0.000 description 3
239000000376 reactant Substances 0.000 description 3
238000001953 recrystallisation Methods 0.000 description 3
239000007858 starting material Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
239000011701 zinc Substances 0.000 description 3
229910052725 zinc Inorganic materials 0.000 description 3
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 2
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
241000233614 Phytophthora Species 0.000 description 2
241000233622 Phytophthora infestans Species 0.000 description 2
235000010582 Pisum sativum Nutrition 0.000 description 2
241001281803 Plasmopara viticola Species 0.000 description 2
241000233639 Pythium Species 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
238000009835 boiling Methods 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
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
239000004927 clay Substances 0.000 description 2
229940125904 compound 1 Drugs 0.000 description 2
229940126214 compound 3 Drugs 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000012990 dithiocarbamate Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
235000019441 ethanol Nutrition 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
235000013312 flour Nutrition 0.000 description 2
230000002538 fungal effect Effects 0.000 description 2
150000008282 halocarbons Chemical class 0.000 description 2
125000000623 heterocyclic group Chemical class 0.000 description 2
SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 2
150000004679 hydroxides Chemical class 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
208000015181 infectious disease Diseases 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
150000004702 methyl esters Chemical class 0.000 description 2
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
150000002790 naphthalenes Chemical class 0.000 description 2
150000004010 onium ions Chemical class 0.000 description 2
239000006072 paste Substances 0.000 description 2
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229920000570 polyether Polymers 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
150000004023 quaternary phosphonium compounds Chemical class 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000002689 soil Substances 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical class CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-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
OIWIYLWZIIJNHU-UHFFFAOYSA-N 1-sulfanylpyrazole Chemical compound SN1C=CC=N1 OIWIYLWZIIJNHU-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
VFTFKUDGYRBSAL-UHFFFAOYSA-N 15-crown-5 Chemical compound C1COCCOCCOCCOCCO1 VFTFKUDGYRBSAL-UHFFFAOYSA-N 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
KBLAMUYRMZPYLS-UHFFFAOYSA-N 2,3-bis(2-methylpropyl)naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 KBLAMUYRMZPYLS-UHFFFAOYSA-N 0.000 description 1
YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
OHDHXJFJWMHFEM-UHFFFAOYSA-N 2-(trichloromethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C(Cl)(Cl)Cl)C(=O)C2=C1 OHDHXJFJWMHFEM-UHFFFAOYSA-N 0.000 description 1
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125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
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OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Adhesives Or Adhesive Processes (AREA)
Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Furan Compounds (AREA)
Pyridine Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

DD79217705A 1978-12-18 1979-12-14 Fungizide mittel DD147807A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782854600 DE2854600A1 (de)	1978-12-18	1978-12-18	Substituierte cyanamide

Publications (1)

Publication Number	Publication Date
DD147807A5 true DD147807A5 (de)	1981-04-22

Family

ID=6057524

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79217705A DD147807A5 (de)	1978-12-18	1979-12-14	Fungizide mittel

Country Status (17)

Country	Link
US (1)	US4235928A (fr)
EP (1)	EP0012428B1 (fr)
JP (1)	JPS5585558A (fr)
AT (1)	ATE64T1 (fr)
AU (1)	AU5385479A (fr)
BR (1)	BR7908263A (fr)
CA (1)	CA1117131A (fr)
CS (1)	CS212332B2 (fr)
DD (1)	DD147807A5 (fr)
DE (2)	DE2854600A1 (fr)
DK (1)	DK536779A (fr)
IE (1)	IE49237B1 (fr)
IL (1)	IL58841A0 (fr)
MA (1)	MA18680A1 (fr)
NZ (1)	NZ192429A (fr)
PL (1)	PL118864B2 (fr)
ZA (1)	ZA796788B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4177149A (en) *	1978-07-21	1979-12-04	Pall Corporation	Filter assembly for intravenous liquid administration apparatus
DE2854599A1 (de) *	1978-12-18	1980-06-26	Basf Ag	Substituierte n-halogenmethylanilide und verfahren zu ihrer herstellung und verwendung
DE3130302A1 (de) *	1981-07-31	1983-02-17	Basf Ag, 6700 Ludwigshafen	N-carbamoylmethyl-haogenacetanilide, verfahren zu ihrer herstellung und diese enthaltende herbizide
DE3134882A1 (de) *	1981-09-03	1983-03-10	Basf Ag, 6700 Ludwigshafen	Oxadiazolcarbonsaeureamide, verfahren zu ihrer herstellung und diese enthaltende fungizide
US4863940A (en) *	1984-07-26	1989-09-05	Rohm And Haas	N-acetonyl-substituted amides and phytopathogenic fungicidal use thereof
US5196046A (en) *	1984-07-26	1993-03-23	Rohm And Haas Company	N-acetonyl-substituted-amides
DE3506814A1 (de) *	1985-02-27	1986-08-28	Basf Ag, 6700 Ludwigshafen	5-isoxazolcarbonsaeureamide, ihre herstellung und verwendung als fungizide
ES2075202T3 (es) *	1989-04-17	1995-10-01	Byk Gulden Lomberg Chem Fab	Nuevas arilpiridazinas, su preparacion, su utilizacion, y medicamentos que las contienen.
US6906069B1 (en)	1999-01-08	2005-06-14	Amgen Inc.	LXR modulators
WO2001060818A1 (fr) *	2000-02-14	2001-08-23	Tularik Inc.	Modulateurs lxr
US6673543B2 (en) *	2000-04-05	2004-01-06	Tularik, Inc.	Solid phase synthesis of LXR ligands
DE10063114A1 (de) *	2000-12-18	2002-06-20	Bayer Ag	Dichlorpyridylmethylcyanamidine
US7112606B2 (en) *	2002-01-30	2006-09-26	Amgen Inc.	Heterocyclic arylsulfonamidobenzylic compounds
US9364773B2 (en)	2013-02-22	2016-06-14	Anschutz Exploration Corporation	Method and system for removing hydrogen sulfide from sour oil and sour water

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1164160A (en) *	1966-12-30	1969-09-17	Shell Int Research	N,N-Disubstituted Amino Acid Derivatives and their use as Herbicides
US3954992A (en) *	1973-07-02	1976-05-04	E. I. Du Pont De Nemours And Company	2-Cyano-2-hydroxyiminoacetamides as plant disease control agents

1978
- 1978-12-18 DE DE19782854600 patent/DE2854600A1/de not_active Withdrawn
1979
- 1979-11-30 US US06/099,017 patent/US4235928A/en not_active Expired - Lifetime
- 1979-11-30 IL IL58841A patent/IL58841A0/xx unknown
- 1979-12-12 DE DE7979105108T patent/DE2960357D1/de not_active Expired
- 1979-12-12 EP EP79105108A patent/EP0012428B1/fr not_active Expired
- 1979-12-12 AT AT79105108T patent/ATE64T1/de not_active IP Right Cessation
- 1979-12-13 CA CA000341806A patent/CA1117131A/fr not_active Expired
- 1979-12-14 ZA ZA00796788A patent/ZA796788B/xx unknown
- 1979-12-14 DD DD79217705A patent/DD147807A5/de unknown
- 1979-12-14 PL PL1979220416A patent/PL118864B2/pl unknown
- 1979-12-14 CS CS798825A patent/CS212332B2/cs unknown
- 1979-12-14 AU AU53854/79A patent/AU5385479A/en not_active Abandoned
- 1979-12-15 MA MA18882A patent/MA18680A1/fr unknown
- 1979-12-17 JP JP16289479A patent/JPS5585558A/ja active Pending
- 1979-12-17 BR BR7908263A patent/BR7908263A/pt unknown
- 1979-12-17 IE IE2435/79A patent/IE49237B1/en unknown
- 1979-12-17 DK DK536779A patent/DK536779A/da unknown
- 1979-12-17 NZ NZ192429A patent/NZ192429A/xx unknown

Also Published As

Publication number	Publication date
ATE64T1 (de)	1981-05-15
NZ192429A (en)	1981-07-13
PL220416A2 (fr)	1980-12-15
ZA796788B (en)	1980-12-31
CS212332B2 (en)	1982-03-26
DE2854600A1 (de)	1980-06-26
US4235928A (en)	1980-11-25
EP0012428A1 (fr)	1980-06-25
AU5385479A (en)	1980-06-26
JPS5585558A (en)	1980-06-27
PL118864B2 (en)	1981-11-30
IL58841A0 (en)	1980-02-29
DK536779A (da)	1980-06-19
CA1117131A (fr)	1982-01-26
BR7908263A (pt)	1980-09-23
DE2960357D1 (en)	1981-08-20
MA18680A1 (fr)	1980-07-01
IE49237B1 (en)	1985-09-04
EP0012428B1 (fr)	1981-05-13
IE792435L (en)	1980-06-18

Publication	Publication Date	Title
EP0012428B1 (fr)	1981-05-13	Cyanamides substituées, procédé pour leur préparation et leur utilisation comme fongicides
EP0013360B1 (fr)	1982-04-07	Anilides carboxyliques N-substitués, procédé pour leur préparation et leur utilisation comme fongicides
EP0026873B1 (fr)	1982-10-06	Anilides d'acides isoxazolecarboxyliques, leur préparation, fungicides les contenant et procédé de lutte contre les champignons
EP0029996B1 (fr)	1983-02-16	Méthyl-2 naphtylamides N-substitués, procédé pour leur préparation et fongicides les contenant
EP0065723B1 (fr)	1984-09-12	2-Méthylnaphtylamides N-substituées, leur préparation et leur emploi comme fongicides
EP0069294A1 (fr)	1983-01-12	2-Méthylnaphtylamides N-substitués, procédé pour leur préparation et fongicides les contenant
EP0039421A1 (fr)	1981-11-11	1-(Trihalogénométhyl-sulfényl)-4-aryl-1,2,4-trazolidin-5-ones, procédé pour leur préparation, fongicides les contenant et procédé de lutte contre les champignons au moyen de ces produits
EP0019745B1 (fr)	1982-07-28	2-Aminopropanalacétals, procédé pour leur préparation, fongicides les contenant, leur préparation et procédé de lutte contre des champignons
EP0088325B1 (fr)	1985-09-11	Oximino-acétamides, leur préparation, leur utilisation et leur composition fongicides
EP0033114B1 (fr)	1983-08-24	Thiourées fongicides substituées, leur préparation, leur utilisation dans la lutte contre les champignons et compositions les contenant
EP0037927A1 (fr)	1981-10-21	2-(N-aryl-, N-isoxazolylcarbonyl)-aminobutyrolactones, procédé pour les préparer et fongicides les contenant
EP0051742B1 (fr)	1985-01-09	(N-aryl-N-thiadiazolyl-1,2,3-carbonyl)-aminobutyrolactones, leur préparation, fongicides les contenant et leur utilisation comme fongicides
EP0073973A1 (fr)	1983-03-16	Anilides d'acides thiazolyl- et isothiazolyl carboxyliques, procédé pour les préparer et leur utilisation comme fongicides
DE3202298A1 (de)	1983-08-18	Neue 5-nitrobenzisothiazol-3-sulfide, ihre herstellung und verwendung zur bekaempfung von fungi
DE3135239A1 (de)	1983-03-17	N-substituierte brenztraubensaeureamide, verfahren zu ihrer herstellung und diese enthaltende fungizide
EP0092095A2 (fr)	1983-10-26	(Trihalométhyl-sulfényl)-1-méthyl-4-imidazole-carboxamide-5 et fongicides les contenant
EP0078999A1 (fr)	1983-05-18	Amides d'acide isoxazoline-2-carboxylique, procédé pour les préparer et fongicides les contenant
EP0074071A1 (fr)	1983-03-16	Oxalamides, procédé pour leur préparation et fongicides les contenant
EP0076382A2 (fr)	1983-04-13	N-alkinyl-N-naphtylamides, procédés pour leur préparation et fongicides les contenant
EP0080080A1 (fr)	1983-06-01	Amides de l'acide isoxazole carboxylique, leur préparation et leur utilisation comme fongicides
DE2939350A1 (de)	1981-04-30	Glykoletheranilide, verfahren zu ihrer herstellung und diese enthaltende fungizide
EP0069293A1 (fr)	1983-01-12	Naphtylamides l'acide glycolétheracétique, procédé pour leur préparation et fongicides les contenant
EP0076915A2 (fr)	1983-04-20	Oxadiazolcarboxamides, leur procédé de préparation et les fongicides les contenant
DD156940A5 (de)	1982-10-06	Fungizide mittel