IL93981A - תולדות 1)אימידאזול-1-איל( או )1, 2,4-טריאזול-1-איל( אתאן, ותכשירים המכילים אותן לקטילת פטריות ולוויסותהגידול של צמחים - Google Patents

תולדות 1)אימידאזול-1-איל( או )1, 2,4-טריאזול-1-איל( אתאן, ותכשירים המכילים אותן לקטילת פטריות ולוויסותהגידול של צמחים

Info

Publication number: IL93981A
Authority: IL; Israel
Prior art keywords: och3; tuted; unsubstituted; radicals; carbon
Prior art date: 1989-05-06

Application number

IL9398190A

Other languages

English (en)

Other versions

IL93981A0 (en

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.)

1989-05-06

Filing date

1990-04-02

Publication date

1994-04-12

1990-04-02 Application filed by Basf Ag filed Critical Basf Ag

1991-01-31 Publication of IL93981A0 publication Critical patent/IL93981A0/xx

1994-04-12 Publication of IL93981A publication Critical patent/IL93981A/he

Links

230000000855 fungicidal effect Effects 0.000 title claims description 13
239000000203 mixture Substances 0.000 title description 21
230000008635 plant growth Effects 0.000 title description 4
230000001105 regulatory effect Effects 0.000 title description 3
FEOIYPLRWRCSMS-UHFFFAOYSA-N 1-ethyl-1,2,4-triazole Chemical class CCN1C=NC=N1 FEOIYPLRWRCSMS-UHFFFAOYSA-N 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 28
-1 aminophenyl Chemical group 0.000 claims description 11
150000003839 salts Chemical class 0.000 claims description 11
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
229910052799 carbon Inorganic materials 0.000 claims description 9
XRPDDDRNQJNHLQ-UHFFFAOYSA-N 2-ethyl-1h-pyrrole Chemical class CCC1=CC=CN1 XRPDDDRNQJNHLQ-UHFFFAOYSA-N 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
241000233866 Fungi Species 0.000 claims description 5
125000003545 alkoxy group Chemical group 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 5
239000000417 fungicide Substances 0.000 claims description 5
229910052751 metal Inorganic materials 0.000 claims description 5
239000002184 metal Substances 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
238000007792 addition Methods 0.000 claims 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
150000004696 coordination complex Chemical class 0.000 claims 3
MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 claims 1
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 91
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 84
101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 description 26
241000196324 Embryophyta Species 0.000 description 22
239000004480 active ingredient Substances 0.000 description 16
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
230000012010 growth Effects 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
239000003630 growth substance Substances 0.000 description 7
239000000243 solution Substances 0.000 description 7
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000002904 solvent Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
239000002689 soil Substances 0.000 description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
235000013399 edible fruits Nutrition 0.000 description 4
239000012074 organic phase Substances 0.000 description 4
229910052700 potassium Inorganic materials 0.000 description 4
239000011591 potassium Substances 0.000 description 4
159000000000 sodium salts Chemical class 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
235000004443 Ricinus communis Nutrition 0.000 description 3
229940125904 compound 1 Drugs 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
239000011707 mineral Substances 0.000 description 3
235000010755 mineral Nutrition 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
239000007921 spray Substances 0.000 description 3
UDQTXCHQKHIQMH-KYGLGHNPSA-N (3ar,5s,6s,7r,7ar)-5-(difluoromethyl)-2-(ethylamino)-5,6,7,7a-tetrahydro-3ah-pyrano[3,2-d][1,3]thiazole-6,7-diol Chemical compound S1C(NCC)=N[C@H]2[C@@H]1O[C@H](C(F)F)[C@@H](O)[C@@H]2O UDQTXCHQKHIQMH-KYGLGHNPSA-N 0.000 description 2
ONNDGYXYNGPSJT-UHFFFAOYSA-N 2,2-diethyl-1,4-dioxane Chemical compound CCC1(CC)COCCO1 ONNDGYXYNGPSJT-UHFFFAOYSA-N 0.000 description 2
ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 2
PYRKKGOKRMZEIT-UHFFFAOYSA-N 2-[6-(2-cyclopropylethoxy)-9-(2-hydroxy-2-methylpropyl)-1h-phenanthro[9,10-d]imidazol-2-yl]-5-fluorobenzene-1,3-dicarbonitrile Chemical compound C1=C2C3=CC(CC(C)(O)C)=CC=C3C=3NC(C=4C(=CC(F)=CC=4C#N)C#N)=NC=3C2=CC=C1OCCC1CC1 PYRKKGOKRMZEIT-UHFFFAOYSA-N 0.000 description 2
TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 2
241000207199 Citrus Species 0.000 description 2
241000221787 Erysiphe Species 0.000 description 2
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
241001330975 Magnaporthe oryzae Species 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 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
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
239000002585 base Substances 0.000 description 2
239000001273 butane Substances 0.000 description 2
159000000007 calcium salts Chemical class 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
235000020971 citrus fruits Nutrition 0.000 description 2
229940125851 compound 27 Drugs 0.000 description 2
229940125936 compound 42 Drugs 0.000 description 2
230000001276 controlling effect Effects 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
230000009746 freeze damage Effects 0.000 description 2
238000003898 horticulture Methods 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000005070 ripening Effects 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
241000894007 species Species 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
239000002699 waste material Substances 0.000 description 2
WKFQMDFSDQFAIC-UHFFFAOYSA-N 2,4-dimethylthiolane 1,1-dioxide Chemical compound CC1CC(C)S(=O)(=O)C1 WKFQMDFSDQFAIC-UHFFFAOYSA-N 0.000 description 1
VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 1
241000223600 Alternaria Species 0.000 description 1
241000221198 Basidiomycota Species 0.000 description 1
241000123650 Botrytis cinerea Species 0.000 description 1
235000006008 Brassica napus var napus Nutrition 0.000 description 1
240000000385 Brassica napus var. napus Species 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000371644 Curvularia ravenelii Species 0.000 description 1
241000510928 Erysiphe necator Species 0.000 description 1
240000009088 Fragaria x ananassa Species 0.000 description 1
241000208818 Helianthus Species 0.000 description 1
235000003222 Helianthus annuus Nutrition 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
240000007817 Olea europaea Species 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
241000315044 Passalora arachidicola Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
241000233622 Phytophthora infestans Species 0.000 description 1
241001281803 Plasmopara viticola Species 0.000 description 1
241000317981 Podosphaera fuliginea Species 0.000 description 1
241001337928 Podosphaera leucotricha Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000221300 Puccinia Species 0.000 description 1
241000228453 Pyrenophora Species 0.000 description 1
241000520648 Pyrenophora teres Species 0.000 description 1
241000231139 Pyricularia Species 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
241001533598 Septoria Species 0.000 description 1
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
241000221566 Ustilago Species 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
239000000370 acceptor Substances 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
238000009835 boiling Methods 0.000 description 1
YFNONBGXNFCTMM-UHFFFAOYSA-N butoxybenzene Chemical group CCCCOC1=CC=CC=C1 YFNONBGXNFCTMM-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052792 caesium Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
244000038559 crop plants Species 0.000 description 1
239000010779 crude oil Substances 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
235000021038 drupes Nutrition 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
210000002615 epidermis Anatomy 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
FKBSHNBSEUWDAC-UHFFFAOYSA-L lithium sodium dihydroxide Chemical compound [Li+].[OH-].[OH-].[Na+] FKBSHNBSEUWDAC-UHFFFAOYSA-L 0.000 description 1
239000000463 material Substances 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000003891 oxalate salts Chemical class 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
230000008121 plant development Effects 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
VLYFRFHWUBBLRR-UHFFFAOYSA-L potassium;sodium;carbonate Chemical compound [Na+].[K+].[O-]C([O-])=O VLYFRFHWUBBLRR-UHFFFAOYSA-L 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
238000004904 shortening Methods 0.000 description 1
ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
235000009518 sodium iodide Nutrition 0.000 description 1
238000005507 spraying Methods 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
238000005728 strengthening Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
230000005068 transpiration Effects 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
230000008511 vegetative development Effects 0.000 description 1
230000009105 vegetative growth Effects 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

IL9398190A 1989-05-06 1990-04-02 תולדות 1)אימידאזול-1-איל( או )1, 2,4-טריאזול-1-איל( אתאן, ותכשירים המכילים אותן לקטילת פטריות ולוויסותהגידול של צמחים IL93981A (he)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3914944A DE3914944A1 (de)	1989-05-06	1989-05-06	Azolylethanderivate und diese enthaltende fungizide und wachstumsregulatoren

Publications (2)

Publication Number	Publication Date
IL93981A0 IL93981A0 (en)	1991-01-31
IL93981A true IL93981A (he)	1994-04-12

Family

ID=6380222

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9398190A IL93981A (he)	1989-05-06	1990-04-02	תולדות 1)אימידאזול-1-איל( או )1, 2,4-טריאזול-1-איל( אתאן, ותכשירים המכילים אותן לקטילת פטריות ולוויסותהגידול של צמחים

Country Status (9)

Country	Link
EP (1)	EP0397005A3 (he)
JP (1)	JPH02306967A (he)
KR (1)	KR900018050A (he)
AU (1)	AU616843B2 (he)
CA (1)	CA2013648A1 (he)
DE (1)	DE3914944A1 (he)
IL (1)	IL93981A (he)
NZ (1)	NZ233565A (he)
ZA (1)	ZA903390B (he)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4009594A1 (de) *	1990-03-26	1991-10-02	Basf Ag	Fungizide azolylethanderivate

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NZ181916A (en) *	1975-09-10	1979-01-11	Ici Ltd	1-substituted-1,2,4-triazoles and fungicidal compositions
EP0091219B1 (en) *	1982-04-01	1987-10-21	Schering Agrochemicals Limited	Heterocyclic fungicidal and growth regulant compounds, and compositions containing them

1989
- 1989-05-06 DE DE3914944A patent/DE3914944A1/de not_active Withdrawn
1990
- 1990-04-02 CA CA002013648A patent/CA2013648A1/en not_active Abandoned
- 1990-04-02 IL IL9398190A patent/IL93981A/he not_active IP Right Cessation
- 1990-04-30 EP EP19900108210 patent/EP0397005A3/de not_active Withdrawn
- 1990-05-02 JP JP2115319A patent/JPH02306967A/ja active Pending
- 1990-05-04 AU AU54677/90A patent/AU616843B2/en not_active Ceased
- 1990-05-04 NZ NZ233565A patent/NZ233565A/en unknown
- 1990-05-04 ZA ZA903390A patent/ZA903390B/xx unknown
- 1990-05-04 KR KR1019900006405A patent/KR900018050A/ko not_active Withdrawn

Also Published As

Publication number	Publication date
KR900018050A (ko)	1990-12-20
ZA903390B (en)	1992-01-29
DE3914944A1 (de)	1990-11-08
AU616843B2 (en)	1991-11-07
CA2013648A1 (en)	1990-11-06
AU5467790A (en)	1990-11-08
EP0397005A2 (de)	1990-11-14
JPH02306967A (ja)	1990-12-20
IL93981A0 (en)	1991-01-31
EP0397005A3 (de)	1991-12-18
NZ233565A (en)	1991-04-26

Legal Events

Date	Code	Title	Description
1997-01-10	RH	Patent void

Publication	Publication Date	Title
KR960005952B1 (ko)	1996-05-06	아졸릴메틸-시클로프로필 유도체, 이의 제조방법 및 이를 함유하는 제제
CS225838B2 (en)	1984-02-13	The fungicide agent and the agent for the regulation of the plant growth
KR0163185B1 (ko)	1998-12-01	치환된 아졸일메틸시클로알칸올 및 이들을 함유하는 살균제
US5057532A (en)	1991-10-15	Azolylethylcyclopropanes and their use thereof as crop protection agents
DD202493A5 (de)	1983-09-21	Mikrobizide und wuchsregulierende mittel
US4384879A (en)	1983-05-24	4-(1H-Azolylmethyl)-1,3-dioxolan-5-one derivatives, production thereof and use thereof as growth regulators and/or microbicides
CA1132578A (en)	1982-09-28	.beta.-TRIAZOLYL OXIMES, AGENTS CONTAINING THEM FOR INFLUENCING THE GROWTH OF PLANTS, AND THEIR USE
JPS61200968A (ja)	1986-09-05	複素環式化合物、その製造方法およびこれを含有する、殺菌または植物生長調整剤組成物
US4969950A (en)	1990-11-13	Triazole compounds and methods for regulating plant growth
AU614430B2 (en)	1991-08-29	Azolylmethylcyclopropanes and their use as crop protection agents
EA019612B1 (ru)	2014-04-30	Замещенные производные фенил(окси/тио)алканолов
US5164408A (en)	1992-11-17	1,2-dihaloazolylethane derivatives and crop protection agents containing them
US5199969A (en)	1993-04-06	Azolylethane derivatives and fungicides and growth regulators containing them
US5084471A (en)	1992-01-28	1-halovinylazoles and fungicides and growth regulators containing these
US5122531A (en)	1992-06-16	Vinylazoles and the use thereof for crop protection
US4512795A (en)	1985-04-23	Norbornane compounds, plant growth regulators containing these compounds, and their intermediates
NZ233565A (en)	1991-04-26	Azolylethane derivatives and fungicidal or plant growth regulating compositions
JPS5815964A (ja)	1983-01-29	置換２−ヒドロキシ−３−アゾリルプロパン誘導体、その製法ならびに該誘導体を含有する殺菌剤および生長調節剤
US4282030A (en)	1981-08-04	Method for plant growth regulation
IL97504A (he)	1995-05-26	תולדות 1-)אימידאזוליל או 1,2,4 - טריאזוליל( אתאן(, הכנתן ותכשירים קוטלי פטריות המכילים אותן
JPH0522715B2 (he)	1993-03-30
DE4038811A1 (de)	1991-06-13	Neue triazole mit den pflanzenwuchs regulierender und hemmender wirkung
JPH01102068A (ja)	1989-04-19	置換トリアゾリルアルカノール類
CS241499B2 (cs)	1986-03-13	Prostředek k regulaci růstu rostlin a fungicidní prostředek a způsob výroby účinné složky