CS236695B2 - Fungicide agent and for regulation of plant growth and production method of its efficient components - Google Patents

Fungicide agent and for regulation of plant growth and production method of its efficient components Download PDF

Info

Publication number: CS236695B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; growth; plants; cycloalkyl; acid
Prior art date: 1981-11-19

Application number

CS828295A

Other languages

Czech (cs)

English (en)

Inventor

Eckart Kranz

Karl H Buechel

Udo Kraatz

Erik Regel

Wilhelm Brandes

Paul-Ernst Frohberger

Klaus Luerssen

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.)

1981-11-19

Filing date

1982-11-19

Publication date

1985-05-15

1982-11-19 Application filed by Bayer Ag filed Critical Bayer Ag

1985-05-15 Publication of CS236695B2 publication Critical patent/CS236695B2/cs

Links

230000008635 plant growth Effects 0.000 title claims description 8
239000000417 fungicide Substances 0.000 title abstract description 4
238000004519 manufacturing process Methods 0.000 title description 5
239000002253 acid Substances 0.000 claims abstract description 22
150000003839 salts Chemical class 0.000 claims abstract description 15
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 4
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 4
150000001875 compounds Chemical class 0.000 claims description 49
239000004480 active ingredient Substances 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 20
150000002576 ketones Chemical class 0.000 claims description 15
238000000034 method Methods 0.000 claims description 13
238000002360 preparation method Methods 0.000 claims description 13
238000006243 chemical reaction Methods 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 7
230000000855 fungicidal effect Effects 0.000 claims description 7
150000001299 aldehydes Chemical class 0.000 claims description 5
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230000001105 regulatory effect Effects 0.000 claims description 4
125000000262 haloalkenyl group Chemical group 0.000 claims description 3
125000004122 cyclic group Chemical group 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims 1
239000005648 plant growth regulator Substances 0.000 abstract description 9
229910052751 metal Chemical class 0.000 abstract description 3
239000002184 metal Chemical class 0.000 abstract description 3
125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
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239000000642 acaricide Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
150000003973 alkyl amines Chemical group 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
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
150000003974 aralkylamines Chemical group 0.000 description 1
150000004982 aromatic amines Chemical group 0.000 description 1
239000002969 artificial stone Substances 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
229910001863 barium hydroxide Inorganic materials 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
239000001273 butane Substances 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000012320 chlorinating reagent Substances 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
229960004106 citric acid Drugs 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
238000000576 coating method Methods 0.000 description 1
150000001868 cobalt Chemical class 0.000 description 1
238000004040 coloring Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
244000038559 crop plants Species 0.000 description 1
238000006731 degradation reaction Methods 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
229940117389 dichlorobenzene Drugs 0.000 description 1
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
231100000676 disease causative agent Toxicity 0.000 description 1
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
230000004345 fruit ripening Effects 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
229960002598 fumaric acid Drugs 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000007954 growth retardant Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000011534 incubation Methods 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
230000036512 infertility Effects 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
229960000448 lactic acid Drugs 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
239000006028 limestone Substances 0.000 description 1
NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 1
150000002689 maleic acids Chemical class 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000002420 orchard Substances 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
238000010422 painting Methods 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920000056 polyoxyethylene ether 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
NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
230000002028 premature Effects 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 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
230000000284 resting effect Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
230000005070 ripening Effects 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
230000007226 seed germination Effects 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
238000004904 shortening Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
229960001367 tartaric acid Drugs 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
230000005068 transpiration Effects 0.000 description 1
FEONEKOZSGPOFN-UHFFFAOYSA-K tribromoiron Chemical compound Br[Fe](Br)Br FEONEKOZSGPOFN-UHFFFAOYSA-K 0.000 description 1
FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
238000009827 uniform distribution 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
- 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
- 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
- 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)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

CS828295A 1981-11-19 1982-11-19 Fungicide agent and for regulation of plant growth and production method of its efficient components CS236695B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813145846 DE3145846A1 (de)	1981-11-19	1981-11-19	Cycloalkyl-((alpha)-triazolyl-ss-hydroxy)-ketone, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide und pflanzenwachstumsregulatoren

Publications (1)

Publication Number	Publication Date
CS236695B2 true CS236695B2 (en)	1985-05-15

Family

ID=6146717

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS828295A CS236695B2 (en)	1981-11-19	1982-11-19	Fungicide agent and for regulation of plant growth and production method of its efficient components

Country Status (19)

Country	Link
US (1)	US4530715A (fr)
EP (1)	EP0080102B1 (fr)
JP (1)	JPS5892668A (fr)
AT (1)	ATE20059T1 (fr)
AU (1)	AU554279B2 (fr)
BR (1)	BR8206678A (fr)
CA (1)	CA1185246A (fr)
CS (1)	CS236695B2 (fr)
DD (1)	DD208531A5 (fr)
DE (2)	DE3145846A1 (fr)
DK (1)	DK514582A (fr)
ES (1)	ES8307767A1 (fr)
GR (1)	GR77760B (fr)
HU (1)	HU188524B (fr)
IL (1)	IL67274A (fr)
NZ (1)	NZ202515A (fr)
PL (1)	PL131544B1 (fr)
PT (1)	PT75818B (fr)
ZA (1)	ZA828493B (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3145857A1 (de) *	1981-11-19	1983-05-26	Bayer Ag, 5090 Leverkusen	Alkylcyloalkyl-triazolylmethyl-ketone und verfahreen zu ihrer herstellung
DE3702920A1 (de) *	1987-01-31	1988-08-11	Bayer Ag	Substituierte hydroxy-azolyl-ketone
ATA136687A (de) *	1987-05-27	1993-09-15	Technica Entwicklung	Verfahren und vorrichtung zum beheben von durch naehrstoff-ueberschuss bedingten belastungen von kulturpflanzen
DE3812967A1 (de) *	1987-06-24	1989-01-05	Bayer Ag	Azolylmethyl-cyclopropyl-derivate
DE4208050A1 (de) *	1992-03-13	1993-09-23	Bayer Ag	Azolylmethyl-fluorcyclopropyl-derivate
TW200307539A (en) *	2002-02-01	2003-12-16	Bristol Myers Squibb Co	Cycloalkyl inhibitors of potassium channel function
EP2654433B1 (fr)	2010-12-21	2017-08-30	Bayer Cropscience LP	Les mutants "papier émeri" de bacillus et des méthodes d'application pour la promotion de la croissance des plantes, de la santé des plants et pour le contrôl des maladies et des parasites
MX2014002890A (es)	2011-09-12	2015-01-19	Bayer Cropscience Lp	Metodo para mejorar la salud y/o promover el crecimiento de una planta y/o mejorar la maduracion de frutos.

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1601453A (en) *	1977-05-05	1981-10-28	Ici Ltd	Triazole and imidazole derivatives useful in agriculture
DE2832233A1 (de) *	1978-07-21	1980-01-31	Bayer Ag	Alpha -azolyl- beta -hydroxy-ketone, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE3002430A1 (de) *	1980-01-24	1981-07-30	Bayer Ag, 5090 Leverkusen	Triazolyl-alkandiol-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide

1981
- 1981-11-19 DE DE19813145846 patent/DE3145846A1/de not_active Withdrawn
1982
- 1982-11-02 US US06/438,448 patent/US4530715A/en not_active Expired - Fee Related
- 1982-11-09 PT PT75818A patent/PT75818B/pt unknown
- 1982-11-09 DE DE8282110296T patent/DE3271447D1/de not_active Expired
- 1982-11-09 AT AT82110296T patent/ATE20059T1/de not_active IP Right Cessation
- 1982-11-09 EP EP82110296A patent/EP0080102B1/fr not_active Expired
- 1982-11-16 DD DD82244913A patent/DD208531A5/de unknown
- 1982-11-16 JP JP57199847A patent/JPS5892668A/ja active Pending
- 1982-11-16 NZ NZ202515A patent/NZ202515A/en unknown
- 1982-11-16 IL IL67274A patent/IL67274A/xx unknown
- 1982-11-17 PL PL1982239079A patent/PL131544B1/pl unknown
- 1982-11-17 GR GR69836A patent/GR77760B/el unknown
- 1982-11-18 BR BR8206678A patent/BR8206678A/pt unknown
- 1982-11-18 CA CA000415878A patent/CA1185246A/fr not_active Expired
- 1982-11-18 ZA ZA828493A patent/ZA828493B/xx unknown
- 1982-11-18 AU AU90706/82A patent/AU554279B2/en not_active Ceased
- 1982-11-18 DK DK514582A patent/DK514582A/da not_active Application Discontinuation
- 1982-11-19 ES ES517513A patent/ES8307767A1/es not_active Expired
- 1982-11-19 HU HU823736A patent/HU188524B/hu unknown
- 1982-11-19 CS CS828295A patent/CS236695B2/cs unknown

Also Published As

Publication number	Publication date
AU9070682A (en)	1983-05-26
CA1185246A (fr)	1985-04-09
HU188524B (en)	1986-04-28
EP0080102A1 (fr)	1983-06-01
DK514582A (da)	1983-05-20
ATE20059T1 (de)	1986-06-15
IL67274A0 (en)	1983-03-31
DE3145846A1 (de)	1983-05-26
ZA828493B (en)	1983-09-28
PL239079A1 (en)	1983-08-15
JPS5892668A (ja)	1983-06-02
PT75818A (en)	1982-12-01
GR77760B (fr)	1984-09-25
AU554279B2 (en)	1986-08-14
DE3271447D1 (en)	1986-07-03
BR8206678A (pt)	1983-10-04
PL131544B1 (en)	1984-11-30
DD208531A5 (de)	1984-04-04
ES517513A0 (es)	1983-08-16
PT75818B (en)	1985-07-26
US4530715A (en)	1985-07-23
IL67274A (en)	1986-02-28
EP0080102B1 (fr)	1986-05-28
ES8307767A1 (es)	1983-08-16
NZ202515A (en)	1985-05-31

Publication	Publication Date	Title
KR960005952B1 (ko)	1996-05-06	아졸릴메틸-시클로프로필 유도체, 이의 제조방법 및 이를 함유하는 제제
US4785002A (en)	1988-11-15	Imidazo-pyrrolo-pyridines useful as fungicidal and growth-regulating agents
CS237335B2 (en)	1985-07-16	Fungicide agent and agent for regulation of growth of plants and processing of active components
CS236870B2 (en)	1985-05-15	Fungicide agent for control of grow of plants and processing of active component
JPH0413349B2 (fr)	1992-03-09
KR840001752B1 (ko)	1984-10-19	1-하이드록시에틸-아졸 유도체의 제조방법
HU194554B (en)	1988-02-29	Fungicide and growth-controlling compositions containing tetrahydrofuran-2-yl-methyl-amine derivatives as active components and process for producing tetrahydrofuran-2-yl-methyl-amine derivatives
CS236888B2 (en)	1985-05-15	Fungicide agent for control of grow of plants and processing of active component
CS236691B2 (en)	1985-05-15	Agent for regulation of plant growth and fungicide agent and production method of its efficient components
CS212287B2 (en)	1982-03-26	Fungicide means and means for regulation of the plant growth and method of making the active substances
JPH0422913B2 (fr)	1992-04-20
US4530715A (en)	1985-07-23	Cycloalkyl (α-triazolyl-β-hydroxy)-ketones as fungicides and plant growth regulators
CS212338B2 (en)	1982-03-26	Means for regulation of the plant growth and fungicide means and method of making the active substance
USRE32796E (en)	1988-12-06	Benzyl-pyrimidinylalkyl-ethers as plant growth regulators and fungicides, and corresponding pyrimidinyl-carbinols
CS230598B2 (en)	1984-08-13	Fungicid agent and for regulation of growing of plants and method manufacture of efficient compound
CS236795B2 (en)	1985-05-15	Fungicide agent for regulation of grow of plants and processing method of active component
US4368202A (en)	1983-01-11	Combating fungi with pyrazole-substituted oximino-cyano-acetamide derivatives
US4469902A (en)	1984-09-04	1-Iodoprop-1-yn-3-ols as plant protection agents
US4622064A (en)	1986-11-11	Triazolo-(3,2-c)perhydroxazin-8-one derivatives and use as fungicides and plant growth regulators
US4291061A (en)	1981-09-22	1H-inden-1-one derivatives, processes for producing them, their use in microbicidal compositions, and for combating microorganisms
US4291046A (en)	1981-09-22	Preparation of novel fungicidally active spiro derivatives of 3-(3,5-dihalogenophenyl)-oxazolidine-2-thion-4-ones
US4689343A (en)	1987-08-25	Novel thiolane-2,4-dione-3-carboxamide fungicides
US4514417A (en)	1985-04-30	Combating fungi with new N-sulphenylated allophanates
US4474808A (en)	1984-10-02	Pesticidally active novel N-sulphenylated biuret-N"-carboxylic acid esters
FI71732B (fi)	1986-10-31	1-hydroxietylazolderivat deras framstaellningsfoerfarande och anvaendning som tillvaextregulerande medel foer vaexter och som fungicider