DD144353A5 - Fungizide mittel - Google Patents

Fungizide mittel Download PDF

Info

Publication number: DD144353A5
Authority: DD; German Democratic Republic
Prior art keywords: ccl; hydroxy; butane; triazol; dimethyl
Prior art date: 1978-06-26

Application number

DD79213816A

Other languages

German (de)

English (en)

Inventor

Wolfgang Kraemer

Karl H Buechel

Engelbert Kuehle

Paul-Ernst Frohberger

Wilhelm Brandes

Original Assignee

Bayer 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.)

1978-06-26

Filing date

1979-06-21

Publication date

1980-10-15

1979-06-21 Application filed by Bayer Ag filed Critical Bayer Ag

1980-10-15 Publication of DD144353A5 publication Critical patent/DD144353A5/de

Links

239000000417 fungicide Substances 0.000 title claims abstract description 8
-1 carbamoyl-triazole-1-ol Chemical compound 0.000 claims abstract description 35
150000003839 salts Chemical class 0.000 claims abstract description 20
229910052736 halogen Chemical group 0.000 claims abstract description 13
150000002367 halogens Chemical group 0.000 claims abstract description 13
125000000217 alkyl group Chemical group 0.000 claims abstract description 12
229910052751 metal Chemical class 0.000 claims abstract description 12
239000002184 metal Chemical class 0.000 claims abstract description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 10
239000002253 acid Substances 0.000 claims abstract description 9
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
239000001257 hydrogen Substances 0.000 claims abstract description 9
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 8
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
239000004606 Fillers/Extenders Substances 0.000 claims abstract description 5
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 5
125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 4
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 4
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 4
125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 4
239000004094 surface-active agent Substances 0.000 claims abstract description 4
238000002360 preparation method Methods 0.000 claims description 15
238000000034 method Methods 0.000 claims description 6
241000233866 Fungi Species 0.000 claims description 4
239000000203 mixture Substances 0.000 abstract description 18
230000000855 fungicidal effect Effects 0.000 abstract description 8
239000003795 chemical substances by application Substances 0.000 abstract description 4
239000000460 chlorine Substances 0.000 description 66
150000001875 compounds Chemical class 0.000 description 47
125000001309 chloro group Chemical group Cl* 0.000 description 35
241000196324 Embryophyta Species 0.000 description 23
206010061217 Infestation Diseases 0.000 description 20
239000004480 active ingredient Substances 0.000 description 17
125000004432 carbon atom Chemical group C* 0.000 description 11
239000002904 solvent Substances 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
238000009472 formulation Methods 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
239000007788 liquid Substances 0.000 description 7
230000001681 protective effect Effects 0.000 description 7
239000007921 spray Substances 0.000 description 7
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
GALVWVNTTXFDBL-UHFFFAOYSA-N 1-phenoxy-1-(2h-triazol-4-yl)butan-2-ol Chemical class C=1NN=NC=1C(C(O)CC)OC1=CC=CC=C1 GALVWVNTTXFDBL-UHFFFAOYSA-N 0.000 description 5
240000008067 Cucumis sativus Species 0.000 description 5
241000221785 Erysiphales Species 0.000 description 5
240000005979 Hordeum vulgare Species 0.000 description 5
239000013543 active substance Substances 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
125000002877 alkyl aryl group Chemical group 0.000 description 5
PVXRCPDNJSFYBV-UHFFFAOYSA-N carbamoyl fluoride Chemical class NC(F)=O PVXRCPDNJSFYBV-UHFFFAOYSA-N 0.000 description 5
235000013339 cereals Nutrition 0.000 description 5
239000003814 drug Substances 0.000 description 5
229940079593 drug Drugs 0.000 description 5
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JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
239000003960 organic solvent Substances 0.000 description 5
229920000151 polyglycol Polymers 0.000 description 5
239000010695 polyglycol Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000002689 soil Substances 0.000 description 5
239000007858 starting material Substances 0.000 description 5
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
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235000007340 Hordeum vulgare Nutrition 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
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150000007513 acids Chemical class 0.000 description 4
239000001273 butane Substances 0.000 description 4
239000000969 carrier Substances 0.000 description 4
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125000001424 substituent group Chemical group 0.000 description 4
239000011701 zinc Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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150000001340 alkali metals Chemical class 0.000 description 3
239000002585 base Substances 0.000 description 3
238000001035 drying Methods 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
DUJBWBJTNVLCLM-UHFFFAOYSA-N n-methyl-n-(trichloromethylsulfanyl)carbamoyl fluoride Chemical compound FC(=O)N(C)SC(Cl)(Cl)Cl DUJBWBJTNVLCLM-UHFFFAOYSA-N 0.000 description 3
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HAGYXNVNFOULKK-UHFFFAOYSA-N 1-trityl-1,2,4-triazole Chemical compound N1=CN=CN1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 HAGYXNVNFOULKK-UHFFFAOYSA-N 0.000 description 2
IPIOZMPHOAYMAQ-UHFFFAOYSA-N 3,3-dimethyl-1-phenoxy-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical class C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=CC=C1 IPIOZMPHOAYMAQ-UHFFFAOYSA-N 0.000 description 2
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
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206010017533 Fungal infection Diseases 0.000 description 2
241000896246 Golovinomyces cichoracearum Species 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
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LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
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GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
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HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
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JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000010410 dusting Methods 0.000 description 2
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150000002148 esters Chemical class 0.000 description 2
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DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 2
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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 2
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DSEWCGHALGPHPT-UHFFFAOYSA-N 1-(4-bromophenoxy)-4-chloro-3-(chloromethyl)-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(CCl)(CCl)C)OC1=CC=C(Br)C=C1 DSEWCGHALGPHPT-UHFFFAOYSA-N 0.000 description 1
RCHYGXSFFHHQSR-UHFFFAOYSA-N 3,3-dimethyl-1-(2-phenylphenoxy)-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=CC=C1C1=CC=CC=C1 RCHYGXSFFHHQSR-UHFFFAOYSA-N 0.000 description 1
KACWPNYTHORXIG-UHFFFAOYSA-N 4-bromo-1-(4-chloro-2-methylphenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol;4-chloro-3-(chloromethyl)-3-methyl-1-phenoxy-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(CCl)(CCl)C)OC1=CC=CC=C1.CC1=CC(Cl)=CC=C1OC(C(O)C(C)(C)CBr)N1N=CN=C1 KACWPNYTHORXIG-UHFFFAOYSA-N 0.000 description 1
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239000011777 magnesium Substances 0.000 description 1
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239000004579 marble Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
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AZFQCTBZOPUVOW-UHFFFAOYSA-N methyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 AZFQCTBZOPUVOW-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
ZUZLIXGTXQBUDC-UHFFFAOYSA-N methyltrioctylammonium Chemical compound CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC ZUZLIXGTXQBUDC-UHFFFAOYSA-N 0.000 description 1
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229910052901 montmorillonite Inorganic materials 0.000 description 1
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
YZMHQCWXYHARLS-UHFFFAOYSA-N naphthalene-1,2-disulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC=C21 YZMHQCWXYHARLS-UHFFFAOYSA-N 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
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239000003208 petroleum Substances 0.000 description 1
DJFBJKSMACBYBD-UHFFFAOYSA-N phosphane;hydrate Chemical class O.P DJFBJKSMACBYBD-UHFFFAOYSA-N 0.000 description 1
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239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
230000000630 rising effect Effects 0.000 description 1
239000011435 rock Substances 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000000779 smoke Substances 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 description 1
238000009331 sowing Methods 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
DTIFFPXSSXFQCJ-UHFFFAOYSA-N tetrahexylazanium Chemical compound CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC DTIFFPXSSXFQCJ-UHFFFAOYSA-N 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
CHYBTAZWINMGHA-UHFFFAOYSA-N tetraoctylazanium Chemical compound CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)CCCCCCCC CHYBTAZWINMGHA-UHFFFAOYSA-N 0.000 description 1
GJSGYPDDPQRWPK-UHFFFAOYSA-N tetrapentylammonium Chemical compound CCCCC[N+](CCCCC)(CCCCC)CCCCC GJSGYPDDPQRWPK-UHFFFAOYSA-N 0.000 description 1
GIZSHQYTTBQKOQ-UHFFFAOYSA-N threo-Syringoylglycerol Chemical compound COC1=CC(C(O)C(O)CO)=CC(OC)=C1O GIZSHQYTTBQKOQ-UHFFFAOYSA-N 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
239000011135 tin Substances 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
OKBQUWUVZGPEQZ-UHFFFAOYSA-N tributyl(hexadecyl)phosphanium Chemical compound CCCCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC OKBQUWUVZGPEQZ-UHFFFAOYSA-N 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 1
WSFDRHZUAHDHDN-UHFFFAOYSA-N trimethyl-[(4-methylphenyl)methyl]azanium Chemical compound CC1=CC=C(C[N+](C)(C)C)C=C1 WSFDRHZUAHDHDN-UHFFFAOYSA-N 0.000 description 1
ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical compound C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- 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
- 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
- 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
- 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

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)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

DD79213816A 1978-06-26 1979-06-21 Fungizide mittel DD144353A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782827968 DE2827968A1 (de)	1978-06-26	1978-06-26	Sulfenylierte carbamoyl-triazolyl- o,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide

Publications (1)

Publication Number	Publication Date
DD144353A5 true DD144353A5 (de)	1980-10-15

Family

ID=6042776

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79213816A DD144353A5 (de)	1978-06-26	1979-06-21	Fungizide mittel

Country Status (10)

Country	Link
US (1)	US4239766A (cs)
EP (1)	EP0006538B1 (cs)
JP (1)	JPS554395A (cs)
BR (1)	BR7903977A (cs)
CS (1)	CS215022B2 (cs)
DD (1)	DD144353A5 (cs)
DE (2)	DE2827968A1 (cs)
DK (1)	DK267279A (cs)
IL (1)	IL57626A0 (cs)
PL (1)	PL115641B1 (cs)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2918894A1 (de) *	1979-05-10	1980-11-20	Bayer Ag	Fluorierte 1-triazolyl-butan-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2918896A1 (de) *	1979-05-10	1980-11-20	Bayer Ag	Antimikrobielle mittel
DE2938534A1 (de) *	1979-09-24	1981-04-23	Bayer Ag, 5090 Leverkusen	Acylierte triazolyl-(gamma)-fluorpinakolyl-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2938575A1 (de) *	1979-09-24	1981-04-23	Bayer Ag, 5090 Leverkusen	Acylierte imidazolyl-(gamma)-fluorpinakolyl-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE3033592A1 (de) *	1980-09-06	1982-04-22	Bayer Ag, 5090 Leverkusen	Fluorierte 1-azolyl-butan-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE3315262A1 (de) *	1983-04-27	1984-10-31	Bayer Ag, 5090 Leverkusen	Carbamoylierte azolylalkyl-phenoxy-carbinole, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenschutzmittel

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AT214708B (de) *	1948-05-18		Exxon Research Engineering Co	Verfahren zur Bekämpfung von Schädlingen
US2553775A (en) *	1949-06-21	1951-05-22	Standard Oil Dev Co	N-thiotrichloromethyl amides and parasiticidal compositions containing them
NL271019A (cs) *	1960-11-03
DE2600799A1 (de) *	1976-01-10	1977-07-14	Bayer Ag	Acylierte triazolyl-0,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2635883A1 (de) *	1976-08-10	1978-02-16	Bayer Ag	N-sulfenylierte oximcarbamate, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide und nematozide
DE2635663A1 (de) *	1976-08-07	1978-02-09	Bayer Ag	Azolyl-carbonsaeure-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2720949A1 (de) *	1977-05-10	1978-11-23	Bayer Ag	Azolylaether-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide

1978
- 1978-06-26 DE DE19782827968 patent/DE2827968A1/de not_active Withdrawn
1979
- 1979-06-07 US US06/046,283 patent/US4239766A/en not_active Expired - Lifetime
- 1979-06-15 DE DE7979101939T patent/DE2961504D1/de not_active Expired
- 1979-06-15 EP EP79101939A patent/EP0006538B1/de not_active Expired
- 1979-06-21 DD DD79213816A patent/DD144353A5/de unknown
- 1979-06-22 IL IL57626A patent/IL57626A0/xx unknown
- 1979-06-23 PL PL1979216553A patent/PL115641B1/pl unknown
- 1979-06-25 JP JP7923679A patent/JPS554395A/ja active Pending
- 1979-06-25 BR BR7903977A patent/BR7903977A/pt unknown
- 1979-06-25 DK DK267279A patent/DK267279A/da unknown
- 1979-06-26 CS CS794398A patent/CS215022B2/cs unknown

Also Published As

Publication number	Publication date
BR7903977A (pt)	1980-03-11
CS215022B2 (en)	1982-06-25
EP0006538B1 (de)	1981-12-02
DK267279A (da)	1979-12-27
PL216553A1 (cs)	1980-03-10
PL115641B1 (en)	1981-04-30
DE2827968A1 (de)	1980-01-10
IL57626A0 (en)	1979-10-31
DE2961504D1 (en)	1982-01-28
EP0006538A1 (de)	1980-01-09
JPS554395A (en)	1980-01-12
US4239766A (en)	1980-12-16

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EP0085333B1 (de)	1986-02-26	Ether-Derivate von substituierten 1-Hydroxyalkyl-azolen, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide und Pflanzenwachstumsregulatoren
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EP0025949B1 (de)	1983-07-20	Acylierte Triazolyl-gamma-fluorpinakolyl-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0019189B1 (de)	1982-07-28	Fungizide Mittel, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0004303B1 (de)	1982-01-13	Acylierte 1-Azolyl-2-hydroxy-butan-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0054865A1 (de)	1982-06-30	Substituierte 1-Azolyl-butan-2-one, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide sowie als Zwischenprodukte
EP0031911B1 (de)	1982-11-17	Substituierte Triazolylmethyl-tert.-butyl-ketone, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenschutzmittel sowie als Zwischenprodukte
EP0032561B1 (de)	1983-05-04	Triazolylphenacyl-pyridyl-ether-Derivate, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0009707B1 (de)	1981-12-23	Halogenierte 1-Azolyl-1-fluorphenoxy-butan-Derivate, Verfahren zu ihrer Herstellung, sie enthaltende Fungizide Mittel sowie ihre Verwendung als Fungizide
EP0006538B1 (de)	1981-12-02	Sulfenylierte Carbamoyl-triazolyl-O,N-acetale, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0042980A2 (de)	1982-01-06	4-Substituierte 1-Azolyl-l-phenoxy-3,3-dimethyl-butan-2-one und -ole, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
DD141255A5 (de)	1980-04-23	Fungizide mittel
EP0040366B1 (de)	1983-11-02	Imidazolyl-vinyl-ketone und -carbinole, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0057864B1 (de)	1984-10-03	2-Azolylmethyl-1,3-dioxolan- und -dioxan-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
DD200215A5 (de)	1983-03-30	Fungizide mittel
EP0040367A1 (de)	1981-11-25	Substituierte Phenyl-triazolyl-vinyl-ketone, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0045016B1 (de)	1984-09-12	Substituierte Triazolylalkyl-pyridyl-ether, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0073331B1 (de)	1986-04-09	5-Aryloxy-5-azolyl-3,3-dimethyl-1-penten-4-one und -ole, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
EP0024538B1 (de)	1983-01-26	1,2,4-Triazolyl-enolether, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0039405A2 (de)	1981-11-11	Triazolyl-benzyloxy-ketone und -carbinole, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide
DE3434158A1 (de)	1986-03-20	Substituierte 1,1-bis-azolyl-butan-2-one und -ole
EP0033087A2 (de)	1981-08-05	Triazolyl-alkandiol-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0065204A2 (de)	1982-11-24	3-Substituierte 1-Azolyl-3-methyl-1-phenoxy-butan-2-one und -ole, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide