DE2431073A1 - Fungizides mittel - Google Patents
Fungizides mittelInfo
- Publication number
- DE2431073A1 DE2431073A1 DE2431073A DE2431073A DE2431073A1 DE 2431073 A1 DE2431073 A1 DE 2431073A1 DE 2431073 A DE2431073 A DE 2431073A DE 2431073 A DE2431073 A DE 2431073A DE 2431073 A1 DE2431073 A1 DE 2431073A1
- Authority
- DE
- Germany
- Prior art keywords
- active ingredient
- phenoxy
- phenyl
- plants
- rust
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 230000000855 fungicidal effect Effects 0.000 title description 7
- 241000221535 Pucciniales Species 0.000 claims description 9
- 239000000417 fungicide Substances 0.000 claims description 6
- 239000004606 Fillers/Extenders Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 2
- 241001295925 Gegenes Species 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 31
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 18
- 241000196324 Embryophyta Species 0.000 description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 206010061217 Infestation Diseases 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 241000221577 Uromyces appendiculatus Species 0.000 description 8
- 239000007921 spray Substances 0.000 description 8
- -1 1- phenyl-phenoxy Chemical group 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- 241000221576 Uromyces Species 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 208000015181 infectious disease Diseases 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 241000233866 Fungi Species 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000011081 inoculation Methods 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 241001123569 Puccinia recondita Species 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical group C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 231100000676 disease causative agent Toxicity 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 230000002464 fungitoxic effect Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 description 1
- PXVMLILXGXVKAT-UHFFFAOYSA-N 3,3-dimethyl-1-(4-phenylphenoxy)butan-2-one Chemical compound C1=CC(OCC(=O)C(C)(C)C)=CC=C1C1=CC=CC=C1 PXVMLILXGXVKAT-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000282376 Panthera tigris Species 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 241000221300 Puccinia Species 0.000 description 1
- 206010037888 Rash pustular Diseases 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 208000024386 fungal infectious disease Diseases 0.000 description 1
- 231100000162 fungitoxic Toxicity 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
- C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/63—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
- C07C45/71—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/20—Unsaturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/255—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing ether groups, groups, groups, or groups
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
- C07D327/04—Five-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (22)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2431073A DE2431073A1 (de) | 1974-06-28 | 1974-06-28 | Fungizides mittel |
GB2226875A GB1448974A (en) | 1974-06-28 | 1975-05-22 | Fungicidal agent |
SE7507347A SE7507347L (sv) | 1974-06-28 | 1975-06-06 | Fungicit medel. |
US05/586,122 US4053616A (en) | 1974-06-28 | 1975-06-11 | Combating rust fungi with 1-[1',2',4'-triazolyl-(1')]-1-(4'-phenyl-phenoxy)-3,3-dimethyl-butan-2-one |
NO752113A NO752113L (en, 2012) | 1974-06-28 | 1975-06-13 | |
CS4359A CS175397B2 (en, 2012) | 1974-06-28 | 1975-06-19 | |
IL47562A IL47562A0 (en) | 1974-06-28 | 1975-06-25 | A method of combating fungi with a certain 1,2,4-triazole derivative |
BE157696A BE830661A (fr) | 1974-06-28 | 1975-06-26 | Nouvelle composition fongicide |
CH832275A CH578301A5 (en, 2012) | 1974-06-28 | 1975-06-26 | |
LU72834A LU72834A1 (en, 2012) | 1974-06-28 | 1975-06-26 | |
BR5135/75D BR7503992A (pt) | 1974-06-28 | 1975-06-26 | Composicoes fungicidas |
TR18507A TR18507A (tr) | 1974-06-28 | 1975-06-26 | Fungisid maddeler |
ZA00754112A ZA754112B (en) | 1974-06-28 | 1975-06-27 | Fungicidal agent |
DK293975A DK136842C (da) | 1974-06-28 | 1975-06-27 | Fungicidt middel med selektiv virkning mod rustsvampe |
OA55539A OA05040A (fr) | 1974-06-28 | 1975-06-27 | Nouvelle composition fongicide. |
JP50079480A JPS5119128A (en, 2012) | 1974-06-28 | 1975-06-27 | |
IE1428/75A IE41173B1 (en) | 1974-06-28 | 1975-06-27 | Fungicidal agent |
FR7520316A FR2275997A1 (fr) | 1974-06-28 | 1975-06-27 | Composition a base de 1-(1,2,4-triazolyl-(1)) - 1 - (4'-phenylphenoxy)-3,3-dimethylbutane-2-one, utilisable selectivement contre les champignons responsables de la rouille |
DD186943A DD121262A5 (en, 2012) | 1974-06-28 | 1975-06-27 | |
AU82562/75A AU483332B2 (en) | 1974-06-28 | 1975-06-30 | Fungicidal agent |
KE2711A KE2711A (en) | 1974-06-28 | 1977-03-15 | Fungicidal agent |
MY257/77A MY7700257A (en) | 1974-06-28 | 1977-12-30 | Fungicidal agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2431073A DE2431073A1 (de) | 1974-06-28 | 1974-06-28 | Fungizides mittel |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2431073A1 true DE2431073A1 (de) | 1976-01-15 |
Family
ID=5919183
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2431073A Pending DE2431073A1 (de) | 1974-06-28 | 1974-06-28 | Fungizides mittel |
Country Status (21)
Country | Link |
---|---|
US (1) | US4053616A (en, 2012) |
JP (1) | JPS5119128A (en, 2012) |
BE (1) | BE830661A (en, 2012) |
BR (1) | BR7503992A (en, 2012) |
CH (1) | CH578301A5 (en, 2012) |
CS (1) | CS175397B2 (en, 2012) |
DD (1) | DD121262A5 (en, 2012) |
DE (1) | DE2431073A1 (en, 2012) |
DK (1) | DK136842C (en, 2012) |
FR (1) | FR2275997A1 (en, 2012) |
GB (1) | GB1448974A (en, 2012) |
IE (1) | IE41173B1 (en, 2012) |
IL (1) | IL47562A0 (en, 2012) |
KE (1) | KE2711A (en, 2012) |
LU (1) | LU72834A1 (en, 2012) |
MY (1) | MY7700257A (en, 2012) |
NO (1) | NO752113L (en, 2012) |
OA (1) | OA05040A (en, 2012) |
SE (1) | SE7507347L (en, 2012) |
TR (1) | TR18507A (en, 2012) |
ZA (1) | ZA754112B (en, 2012) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0001571A1 (de) * | 1977-10-12 | 1979-05-02 | BASF Aktiengesellschaft | Phenylazophenyloxy-triazolylverbindungen und Fungizide, die diese Verbindungen enthalten |
US4178383A (en) | 1976-05-28 | 1979-12-11 | Bayer Aktiengesellschaft | Fungicidally active oxime-ethers of isonitrosocyanoacetamides |
EP0007506A1 (de) * | 1978-07-21 | 1980-02-06 | Bayer Ag | Alpha-Azolyl-keto-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide |
EP0010691A1 (de) * | 1978-10-23 | 1980-05-14 | BASF Aktiengesellschaft | Neue 1,2,4-Triazolderivate Verfahren zu ihrer Herstellung, ihre Verwendung zur Herstellung von Pflanzenschutzmitteln, Verfahren zur Herstellung von Fungiziden und Verfahren zur Bekämpfung von Fungi sowie fungizide Mittel |
EP0040350A1 (de) * | 1980-05-19 | 1981-11-25 | BASF Aktiengesellschaft | Neue Azolverbindungen, ihre Herstellung, ihre Verwendung zur Pflanzenbehandlung und Mittel dafür |
RU2363157C1 (ru) * | 2008-03-24 | 2009-08-10 | Федеральное государственное образовательное учреждение высшего профессионального образования "Горский государственный аграрный университет" | Способ защиты зерна от болезней при хранении |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2713777C3 (de) * | 1977-03-29 | 1979-10-31 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von l-Azolyl-33-dimethyl-l-phenoxy-butan-2-onen |
EP0007707A1 (en) * | 1978-07-27 | 1980-02-06 | Imperial Chemical Industries Plc | 1,3-Diazol- and 1,2,4-triazol-derivatives, processes for their preparation, pesticidal compositions containing them and methods of combating pests |
DE3208142A1 (de) * | 1982-03-06 | 1983-09-08 | Bayer Ag, 5090 Leverkusen | Fungizide mittel |
US4642385A (en) * | 1985-11-19 | 1987-02-10 | Mobay Corporation | Preparation of monochloropinacolone |
WO1988007813A1 (en) * | 1987-04-14 | 1988-10-20 | Greencare Pty. Limited | Soil spreader |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3912752A (en) * | 1972-01-11 | 1975-10-14 | Bayer Ag | 1-Substituted-1,2,4-triazoles |
-
1974
- 1974-06-28 DE DE2431073A patent/DE2431073A1/de active Pending
-
1975
- 1975-05-22 GB GB2226875A patent/GB1448974A/en not_active Expired
- 1975-06-06 SE SE7507347A patent/SE7507347L/xx unknown
- 1975-06-11 US US05/586,122 patent/US4053616A/en not_active Expired - Lifetime
- 1975-06-13 NO NO752113A patent/NO752113L/no unknown
- 1975-06-19 CS CS4359A patent/CS175397B2/cs unknown
- 1975-06-25 IL IL47562A patent/IL47562A0/xx unknown
- 1975-06-26 TR TR18507A patent/TR18507A/xx unknown
- 1975-06-26 LU LU72834A patent/LU72834A1/xx unknown
- 1975-06-26 BR BR5135/75D patent/BR7503992A/pt unknown
- 1975-06-26 BE BE157696A patent/BE830661A/xx unknown
- 1975-06-26 CH CH832275A patent/CH578301A5/xx not_active IP Right Cessation
- 1975-06-27 ZA ZA00754112A patent/ZA754112B/xx unknown
- 1975-06-27 DK DK293975A patent/DK136842C/da active
- 1975-06-27 JP JP50079480A patent/JPS5119128A/ja active Pending
- 1975-06-27 FR FR7520316A patent/FR2275997A1/fr not_active Withdrawn
- 1975-06-27 DD DD186943A patent/DD121262A5/xx unknown
- 1975-06-27 OA OA55539A patent/OA05040A/xx unknown
- 1975-06-27 IE IE1428/75A patent/IE41173B1/xx unknown
-
1977
- 1977-03-15 KE KE2711A patent/KE2711A/xx unknown
- 1977-12-30 MY MY257/77A patent/MY7700257A/xx unknown
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4178383A (en) | 1976-05-28 | 1979-12-11 | Bayer Aktiengesellschaft | Fungicidally active oxime-ethers of isonitrosocyanoacetamides |
EP0001571A1 (de) * | 1977-10-12 | 1979-05-02 | BASF Aktiengesellschaft | Phenylazophenyloxy-triazolylverbindungen und Fungizide, die diese Verbindungen enthalten |
EP0007506A1 (de) * | 1978-07-21 | 1980-02-06 | Bayer Ag | Alpha-Azolyl-keto-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide |
EP0010691A1 (de) * | 1978-10-23 | 1980-05-14 | BASF Aktiengesellschaft | Neue 1,2,4-Triazolderivate Verfahren zu ihrer Herstellung, ihre Verwendung zur Herstellung von Pflanzenschutzmitteln, Verfahren zur Herstellung von Fungiziden und Verfahren zur Bekämpfung von Fungi sowie fungizide Mittel |
EP0040350A1 (de) * | 1980-05-19 | 1981-11-25 | BASF Aktiengesellschaft | Neue Azolverbindungen, ihre Herstellung, ihre Verwendung zur Pflanzenbehandlung und Mittel dafür |
US4380546A (en) * | 1980-05-19 | 1983-04-19 | Basf Aktiengesellschaft | Azole compounds, their preparation, their use for crop treatment, and agents for this purpose |
RU2363157C1 (ru) * | 2008-03-24 | 2009-08-10 | Федеральное государственное образовательное учреждение высшего профессионального образования "Горский государственный аграрный университет" | Способ защиты зерна от болезней при хранении |
Also Published As
Publication number | Publication date |
---|---|
JPS5119128A (en, 2012) | 1976-02-16 |
IE41173L (en) | 1975-12-28 |
KE2711A (en) | 1977-04-01 |
DK136842B (da) | 1977-12-05 |
BE830661A (fr) | 1975-12-29 |
MY7700257A (en) | 1977-12-31 |
IL47562A0 (en) | 1975-08-31 |
FR2275997A1 (fr) | 1976-01-23 |
OA05040A (fr) | 1980-12-31 |
BR7503992A (pt) | 1976-06-29 |
US4053616A (en) | 1977-10-11 |
AU8256275A (en) | 1977-01-06 |
LU72834A1 (en, 2012) | 1976-04-13 |
GB1448974A (en) | 1976-09-08 |
TR18507A (tr) | 1977-03-04 |
IE41173B1 (en) | 1979-11-07 |
CH578301A5 (en, 2012) | 1976-08-13 |
CS175397B2 (en, 2012) | 1977-05-31 |
SE7507347L (sv) | 1975-12-29 |
DK293975A (da) | 1975-12-29 |
NO752113L (en, 2012) | 1975-12-30 |
DK136842C (da) | 1978-07-03 |
ZA754112B (en) | 1976-06-30 |
DD121262A5 (en, 2012) | 1976-07-20 |
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