DD239328A5 - Pflanzenwachstumsregulierendes mittel - Google Patents

Pflanzenwachstumsregulierendes mittel Download PDF

Info

Publication number: DD239328A5
Authority: DD; German Democratic Republic
Prior art keywords: methyl; ester; dihydro; dose; plant growth
Prior art date: 1984-07-18

Application number

DD85278628A

Other languages

German (de)

English (en)

Inventor

Sandor Balint

Judit Bencsik

Jozsef Fodor

Andras Horvath

Elemer Toemoerdi

Csaba Soeptei

Jozsef Karsai

Endre Sebestyen

Sandor Gaal

Ivan Gardi

Gyoergy Kis

Andras Papp

Imre Csatlos

Original Assignee

��@��k��

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.)

1984-07-18

Filing date

1985-07-16

Publication date

1986-09-24

1985-07-16 Application filed by ��@��k�� filed Critical ��@��k��

1986-09-24 Publication of DD239328A5 publication Critical patent/DD239328A5/de

Links

230000008635 plant growth Effects 0.000 title claims abstract description 21
230000001105 regulatory effect Effects 0.000 title claims abstract description 12
150000001875 compounds Chemical class 0.000 claims abstract description 37
239000004480 active ingredient Substances 0.000 claims abstract description 19
-1 hydroxy-alkyl phosphonic acid derivatives Chemical class 0.000 abstract description 47
239000003795 chemical substances by application Substances 0.000 abstract description 20
239000001257 hydrogen Substances 0.000 abstract description 4
229910052739 hydrogen Inorganic materials 0.000 abstract description 4
150000001768 cations Chemical class 0.000 abstract description 3
125000001188 haloalkyl group Chemical group 0.000 abstract description 3
125000006526 (C1-C2) alkyl group Chemical group 0.000 abstract 1
125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 abstract 1
125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 65
238000011282 treatment Methods 0.000 description 49
150000002148 esters Chemical class 0.000 description 42
241000196324 Embryophyta Species 0.000 description 36
230000000694 effects Effects 0.000 description 29
240000003768 Solanum lycopersicum Species 0.000 description 27
230000012010 growth Effects 0.000 description 26
238000012360 testing method Methods 0.000 description 25
235000007688 Lycopersicon esculentum Nutrition 0.000 description 23
238000002360 preparation method Methods 0.000 description 20
HSPWOFDKASGERG-UHFFFAOYSA-N 2-chloroethyl-[(2,2-dimethyl-3h-1-benzofuran-7-yl)oxy]phosphinic acid Chemical compound C1=CC(OP(O)(=O)CCCl)=C2OC(C)(C)CC2=C1 HSPWOFDKASGERG-UHFFFAOYSA-N 0.000 description 18
239000000203 mixture Substances 0.000 description 18
HSHNITRMYYLLCV-UHFFFAOYSA-N 4-methylumbelliferone Chemical compound C1=C(O)C=CC2=C1OC(=O)C=C2C HSHNITRMYYLLCV-UHFFFAOYSA-N 0.000 description 16
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
230000008859 change Effects 0.000 description 14
239000002689 soil Substances 0.000 description 14
244000068988 Glycine max Species 0.000 description 13
235000003222 Helianthus annuus Nutrition 0.000 description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
238000002474 experimental method Methods 0.000 description 12
WJGPNUBJBMCRQH-UHFFFAOYSA-N 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-ol Chemical compound C1=CC(O)=C2OC(C)(C)CC2=C1 WJGPNUBJBMCRQH-UHFFFAOYSA-N 0.000 description 11
235000010469 Glycine max Nutrition 0.000 description 8
241000208818 Helianthus Species 0.000 description 8
241000209140 Triticum Species 0.000 description 8
235000021307 Triticum Nutrition 0.000 description 8
239000007921 spray Substances 0.000 description 8
IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
244000020551 Helianthus annuus Species 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
238000000034 method Methods 0.000 description 5
238000005507 spraying Methods 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
YTPMCWYIRHLEGM-BQYQJAHWSA-N 1-[(e)-2-propylsulfonylethenyl]sulfonylpropane Chemical compound CCCS(=O)(=O)\C=C\S(=O)(=O)CCC YTPMCWYIRHLEGM-BQYQJAHWSA-N 0.000 description 4
229920001213 Polysorbate 20 Polymers 0.000 description 4
239000000969 carrier Substances 0.000 description 4
238000010410 dusting Methods 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 4
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 4
230000009467 reduction Effects 0.000 description 4
239000007787 solid Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 3
235000002566 Capsicum Nutrition 0.000 description 3
240000004160 Capsicum annuum Species 0.000 description 3
235000008534 Capsicum annuum var annuum Nutrition 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
239000002253 acid Substances 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 3
239000001511 capsicum annuum Substances 0.000 description 3
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 3
230000000994 depressogenic effect Effects 0.000 description 3
238000011161 development Methods 0.000 description 3
230000004720 fertilization Effects 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
229920005610 lignin Polymers 0.000 description 3
239000011707 mineral Substances 0.000 description 3
230000004048 modification Effects 0.000 description 3
238000012986 modification Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000002426 superphosphate Substances 0.000 description 3
HBEDSQVIWPRPAY-UHFFFAOYSA-N 2,3-dihydrobenzofuran Chemical compound C1=CC=C2OCCC2=C1 HBEDSQVIWPRPAY-UHFFFAOYSA-N 0.000 description 2
125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 2
239000006002 Pepper Substances 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
235000016761 Piper aduncum Nutrition 0.000 description 2
235000017804 Piper guineense Nutrition 0.000 description 2
244000203593 Piper nigrum Species 0.000 description 2
235000008184 Piper nigrum Nutrition 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
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
230000009471 action Effects 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 2
238000009835 boiling Methods 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
150000008371 chromenes Chemical class 0.000 description 2
230000007423 decrease Effects 0.000 description 2
239000003814 drug Substances 0.000 description 2
229940079593 drug Drugs 0.000 description 2
239000007789 gas Substances 0.000 description 2
150000002431 hydrogen Chemical group 0.000 description 2
235000009973 maize Nutrition 0.000 description 2
125000004430 oxygen atom Chemical group O* 0.000 description 2
239000000843 powder Substances 0.000 description 2
230000001603 reducing effect Effects 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
239000004550 soluble concentrate Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
OBGFMRSXJROQDT-UHFFFAOYSA-N 1-methoxy-1-methylurea Chemical compound CON(C)C(N)=O OBGFMRSXJROQDT-UHFFFAOYSA-N 0.000 description 1
OWRHJTUZVUYYNA-UHFFFAOYSA-N 1-methoxy-3-methylurea Chemical compound CNC(=O)NOC OWRHJTUZVUYYNA-UHFFFAOYSA-N 0.000 description 1
UJMGZPCKYHBCKU-UHFFFAOYSA-N 2,2-dimethyl-2,3-dihydrobenzofuran Chemical compound C1=CC=C2OC(C)(C)CC2=C1 UJMGZPCKYHBCKU-UHFFFAOYSA-N 0.000 description 1
WUDQPDHAFHIDFS-UHFFFAOYSA-N 2,3-dimethyl-1-benzofuran-7-ol Chemical compound C1=CC=C2C(C)=C(C)OC2=C1O WUDQPDHAFHIDFS-UHFFFAOYSA-N 0.000 description 1
GRDRTFJXTRZQBB-UHFFFAOYSA-N 2,6-dinitro-N,N-di(propan-2-yl)-4-(trifluoromethyl)aniline Chemical compound [N+](=O)([O-])C1=C(N(C(C)C)C(C)C)C(=CC(=C1)C(F)(F)F)[N+](=O)[O-] GRDRTFJXTRZQBB-UHFFFAOYSA-N 0.000 description 1
GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 1
WVXJJIDYNINQTJ-UHFFFAOYSA-N 2-chloroethyl-(4-methyl-2-oxochromen-7-yl)oxyphosphinic acid Chemical compound C1=C(OP(O)(=O)CCCl)C=CC2=C1OC(=O)C=C2C WVXJJIDYNINQTJ-UHFFFAOYSA-N 0.000 description 1
244000291564 Allium cepa Species 0.000 description 1
235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
244000099147 Ananas comosus Species 0.000 description 1
235000007119 Ananas comosus Nutrition 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
LRHPLDYGYMQRHN-UHFFFAOYSA-N Butanol Natural products CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
PQMOXTJVIYEOQL-UHFFFAOYSA-N Cumarin Natural products CC(C)=CCC1=C(O)C(C(=O)C(C)CC)=C(O)C2=C1OC(=O)C=C2CCC PQMOXTJVIYEOQL-UHFFFAOYSA-N 0.000 description 1
244000043261 Hevea brasiliensis Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
FSOGIJPGPZWNGO-UHFFFAOYSA-N Meomammein Natural products CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C(O)C2=C1OC(=O)C=C2CCC FSOGIJPGPZWNGO-UHFFFAOYSA-N 0.000 description 1
241001024327 Oenanthe <Aves> Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
241000758706 Piperaceae Species 0.000 description 1
240000004713 Pisum sativum Species 0.000 description 1
235000010582 Pisum sativum Nutrition 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
239000013504 Triton X-100 Substances 0.000 description 1
229920004890 Triton X-100 Polymers 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
239000013543 active substance Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
AQKNQRMIGNOQQF-UHFFFAOYSA-N azane;2-(2,4-dichlorophenoxy)acetic acid Chemical compound [NH4+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl AQKNQRMIGNOQQF-UHFFFAOYSA-N 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
230000034303 cell budding Effects 0.000 description 1
230000002301 combined effect Effects 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
230000001276 controlling effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
229960000956 coumarin Drugs 0.000 description 1
235000001671 coumarin Nutrition 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
125000002993 cycloalkylene group Chemical group 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
210000005069 ears Anatomy 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003895 organic fertilizer Substances 0.000 description 1
AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 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
239000003415 peat Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000035790 physiological processes and functions Effects 0.000 description 1
230000008569 process Effects 0.000 description 1
239000000047 product Substances 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000012262 resinous product Substances 0.000 description 1
CQRYARSYNCAZFO-UHFFFAOYSA-N salicyl alcohol Chemical compound OCC1=CC=CC=C1O CQRYARSYNCAZFO-UHFFFAOYSA-N 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
235000013599 spices Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
239000000725 suspension Substances 0.000 description 1
150000007970 thio esters Chemical class 0.000 description 1
HYYHSPXOZWOGDM-UHFFFAOYSA-N toluene 3,5,5-trimethylcyclohex-2-en-1-one Chemical compound O=C1C=C(CC(C)(C)C1)C.C1(=CC=CC=C1)C HYYHSPXOZWOGDM-UHFFFAOYSA-N 0.000 description 1
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1

Classifications

- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing heterocyclic radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring
- C07F9/65517—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring condensed with carbocyclic rings or carbocyclic ring systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/6552—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring
- C07F9/65522—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring condensed with carbocyclic rings or carbocyclic ring systems

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Dentistry (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Fertilizers (AREA)

DD85278628A 1984-07-18 1985-07-16 Pflanzenwachstumsregulierendes mittel DD239328A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU842800A HU190579B (en)	1984-07-18	1984-07-18	Plant growth regulating compositions comprising etherified hydroxy-alkyl-phosphonic acid-derivatives as active substance

Publications (1)

Publication Number	Publication Date
DD239328A5 true DD239328A5 (de)	1986-09-24

Family

ID=10961156

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85278628A DD239328A5 (de)	1984-07-18	1985-07-16	Pflanzenwachstumsregulierendes mittel

Country Status (14)

Country	Link
US (1)	US4668274A (fr)
EP (1)	EP0188502B1 (fr)
JP (1)	JPS61502753A (fr)
AT (1)	ATE41010T1 (fr)
BG (1)	BG51235A3 (fr)
CS (1)	CS256391B2 (fr)
DD (1)	DD239328A5 (fr)
DE (1)	DE3568439D1 (fr)
DK (1)	DK124086A (fr)
ES (1)	ES8700266A1 (fr)
HU (1)	HU190579B (fr)
RO (1)	RO94902B (fr)
SU (1)	SU1486049A3 (fr)
WO (1)	WO1986000904A1 (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
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DE4134158C2 (de) *	1991-10-11	1997-02-13	Max Delbrueck Centrum	Verwendung von Carboplatin in lyotrophen Mesophasen zur Überwindung einer durch Zytostatika ausgelösten Leukopenie
JP2008530221A (ja) *	2005-02-17	2008-08-07	バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト	（二置換プロペニル）フェニルアルキル置換ジヒドロベンゾフランを調製するための改善された方法
EP1853577A4 (fr) *	2005-02-17	2009-02-18	Bayer Cropscience Ag	Procede ameliore de preparation de dihydrobenzofuranes a substitution phenylalkyle (disubstitution propenyle)
WO2006102387A1 (fr) *	2005-03-23	2006-09-28	Bayer Cropscience Ag	Procede ameliore pour la preparation de dihydrobenzofuranes (propenyle disubstitue) a substitution phenylakyle
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.

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DD132632A1 (de) *	1977-08-12	1978-10-18	Bernhard Hesse	Mittel zur beeinflussung des pflanzenwachstums
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1984
- 1984-07-18 HU HU842800A patent/HU190579B/hu not_active IP Right Cessation
1985
- 1985-07-12 AT AT85903355T patent/ATE41010T1/de not_active IP Right Cessation
- 1985-07-12 DE DE8585903355T patent/DE3568439D1/de not_active Expired
- 1985-07-12 EP EP85903355A patent/EP0188502B1/fr not_active Expired
- 1985-07-12 WO PCT/HU1985/000044 patent/WO1986000904A1/fr not_active Ceased
- 1985-07-12 JP JP60503198A patent/JPS61502753A/ja active Pending
- 1985-07-12 RO RO122624A patent/RO94902B/ro unknown
- 1985-07-16 DD DD85278628A patent/DD239328A5/de not_active IP Right Cessation
- 1985-07-17 US US06/839,499 patent/US4668274A/en not_active Expired - Fee Related
- 1985-07-18 ES ES545631A patent/ES8700266A1/es not_active Expired
- 1985-07-18 CS CS855347A patent/CS256391B2/cs unknown
1986
- 1986-03-17 SU SU864027203A patent/SU1486049A3/ru active
- 1986-03-18 DK DK124086A patent/DK124086A/da not_active Application Discontinuation
- 1986-03-18 BG BG074117A patent/BG51235A3/bg unknown

Also Published As

Publication number	Publication date
ES8700266A1 (es)	1986-10-01
US4668274A (en)	1987-05-26
HU190579B (en)	1986-09-29
DK124086D0 (da)	1986-03-18
DK124086A (da)	1986-03-18
DE3568439D1 (en)	1989-04-06
ATE41010T1 (de)	1989-03-15
SU1486049A3 (ru)	1989-06-07
JPS61502753A (ja)	1986-11-27
RO94902B (ro)	1988-08-17
WO1986000904A1 (fr)	1986-02-13
BG51235A3 (bg)	1993-03-15
EP0188502B1 (fr)	1989-03-01
CS256391B2 (en)	1988-04-15
RO94902A (fr)	1988-08-15
EP0188502A1 (fr)	1986-07-30
ES545631A0 (es)	1986-10-01

Legal Events

Date	Code	Title	Description
2002-05-08	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE3177314T2 (de)	1996-09-19	Optisch isomeres Triazolylpentenol. Verfahren zur Herstellung und Verwendung als Fungizid, Herbizid und/oder Wachstumsregulator
DE1567212B2 (de)	1973-09-13	Fungicides Mittel mit bactencider Nebenwirkung
CH644371A5 (de)	1984-07-31	In 2- und 4-stellung disubstituierte 5-thiazolcarbonsaeuren und deren funktionelle derivate.
DE3688844T2 (de)	1994-01-05	Synergistische, herbizide Kombinationen und Verfahren zur Anwendung.
DE1245206B (de)	1967-07-20	Insektenbekaempfungsmittel
DE2514402A1 (de)	1976-10-21	Insektizide mittel
DD149935A5 (de)	1981-08-05	Verfahren zur herstellung von racemen oder optisch aktivem 2-(propargyloxyimino)-1,7,7-trimethylbicyclo(2,2,1)heptan
DD153845A5 (de)	1982-02-03	Verfahren zur herstellung unsymmetrischer thiophosphonatverbindungen
EP0272542B1 (fr)	1993-03-10	Agent d'abscission de parties de plantes
CH632997A5 (en)	1982-11-15	Plant growth regulator
DD251067A5 (de)	1987-11-04	Herbizide zusammensetzung
DD262992A5 (de)	1988-12-21	Nematizide und insektizide zusammensetzung
DD218268A5 (de)	1985-02-06	Herbizide zusammensetzung
CS256391B2 (en)	1988-04-15	Agent for plants growing regulation
DE3300056C2 (de)	1985-06-27	3-Nitrobenzolsulfonanilid-Derivate und diese enthaltende fungizide Mittel
DE2362333C3 (de)	1978-07-13	Thionophosphorsäureesteramide, Verfahren zu deren Herstellung und Verwendung derselben
DD238910A5 (de)	1986-09-10	Pflanzenwachstumsregulierende mittel
DE2635967A1 (de)	1977-03-17	2-cyanacetamid-derivate und ihre herstellung und anwendung
DD236868A5 (de)	1986-06-25	Mittel zum protahieren der wirkungsdauer und zur erhoehung der selektivitaet von herbiziden zusammensetzungen
DE2548898A1 (de)	1976-05-06	Benzothiazolderivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE2513652A1 (de)	1975-10-09	6,8-dichlor-3-methyl-4-chromonoxim, verfahren zur herstellung desselben und fungizide mittel
EP0092632B1 (fr)	1985-09-04	Nouveaux dérivés du benzonitrile, méthode de leur préparation et compositions herbicides
DE2154634A1 (fr)	1972-05-10
DE4011781A1 (de)	1990-10-31	Herbizides mittel
DE2348022A1 (de)	1975-04-03	Sulfonamid-zubereitungen fuer herbicide