CS256391B2 - Agent for plants growing regulation - Google Patents

Agent for plants growing regulation Download PDF

Info

Publication number: CS256391B2
Authority: CS; Czechoslovakia
Prior art keywords: methyl; dihydro; growth; dimethyl; chloroethylphosphonic acid
Prior art date: 1984-07-18

Application number

CS855347A

Other languages

Czech (cs)

English (en)

Inventor

Sandor Balint

Judit Bencsik

Ferenc Fodor

Andras Horvath

Elemer Toemoerdi

Csaba Soeptei

Jozsef Karsai

Endre Sebestyen

Sandor Gaal

Ivan Gardi

Gyoergy Kiss

Andras Papp

Imre Csatlos

Original Assignee

Nitrokemia Ipartelepek

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

1985-07-18

Publication date

1988-04-15

1985-07-18 Application filed by Nitrokemia Ipartelepek filed Critical Nitrokemia Ipartelepek

1988-04-15 Publication of CS256391B2 publication Critical patent/CS256391B2/cs

Links

230000033228 biological regulation Effects 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 42
-1 hydroxy-alkyl phosphonic acid derivatives Chemical class 0.000 claims abstract description 32
239000004480 active ingredient Substances 0.000 claims abstract description 14
230000008635 plant growth Effects 0.000 claims abstract description 10
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
239000001257 hydrogen Substances 0.000 claims abstract description 4
125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 2
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical class OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 claims description 44
238000002360 preparation method Methods 0.000 claims description 25
HSHNITRMYYLLCV-UHFFFAOYSA-N 4-methylumbelliferone Chemical compound C1=C(O)C=CC2=C1OC(=O)C=C2C HSHNITRMYYLLCV-UHFFFAOYSA-N 0.000 claims description 19
239000000203 mixture Substances 0.000 claims description 12
239000007788 liquid Substances 0.000 claims description 11
239000002253 acid Substances 0.000 claims description 8
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 claims description 7
LOUZURPQCYZSJH-UHFFFAOYSA-N 1-chloro-2-dichlorophosphorylethane Chemical compound ClCCP(Cl)(Cl)=O LOUZURPQCYZSJH-UHFFFAOYSA-N 0.000 claims description 4
239000011230 binding agent Substances 0.000 claims description 4
238000000034 method Methods 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 2
239000007787 solid Substances 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
239000000969 carrier Substances 0.000 claims 1
150000008028 secondary esters Chemical group 0.000 claims 1
230000001105 regulatory effect Effects 0.000 abstract description 2
125000006526 (C1-C2) alkyl group Chemical group 0.000 abstract 1
125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
150000001768 cations Chemical class 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 abstract 1
125000001188 haloalkyl group Chemical group 0.000 abstract 1
230000012010 growth Effects 0.000 description 37
238000011282 treatment Methods 0.000 description 31
241000196324 Embryophyta Species 0.000 description 27
240000003768 Solanum lycopersicum Species 0.000 description 26
235000007688 Lycopersicon esculentum Nutrition 0.000 description 25
238000012360 testing method Methods 0.000 description 18
244000068988 Glycine max Species 0.000 description 17
235000010469 Glycine max Nutrition 0.000 description 17
230000008859 change Effects 0.000 description 17
238000003306 harvesting Methods 0.000 description 17
235000003222 Helianthus annuus Nutrition 0.000 description 14
229910019142 PO4 Inorganic materials 0.000 description 13
230000000694 effects Effects 0.000 description 13
239000010452 phosphate Substances 0.000 description 13
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
239000002689 soil Substances 0.000 description 10
244000020551 Helianthus annuus Species 0.000 description 8
239000013543 active substance Substances 0.000 description 8
230000002829 reductive effect Effects 0.000 description 8
239000007921 spray Substances 0.000 description 8
235000008534 Capsicum annuum var annuum Nutrition 0.000 description 6
241000208818 Helianthus Species 0.000 description 6
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-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
238000005507 spraying Methods 0.000 description 6
240000004160 Capsicum annuum Species 0.000 description 5
235000007862 Capsicum baccatum Nutrition 0.000 description 5
241000209140 Triticum Species 0.000 description 5
235000021307 Triticum Nutrition 0.000 description 5
239000001728 capsicum frutescens Substances 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
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 5
239000000126 substance Substances 0.000 description 5
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 4
229920001213 Polysorbate 20 Polymers 0.000 description 4
240000008042 Zea mays Species 0.000 description 4
235000002017 Zea mays subsp mays Nutrition 0.000 description 4
230000004720 fertilization Effects 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 4
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 4
239000000843 powder 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
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
230000004071 biological effect Effects 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
230000007423 decrease Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
238000009472 formulation Methods 0.000 description 3
230000009036 growth inhibition Effects 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
235000009973 maize Nutrition 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000005648 plant growth regulator Substances 0.000 description 3
239000001103 potassium chloride Substances 0.000 description 3
235000011164 potassium chloride Nutrition 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
239000002426 superphosphate Substances 0.000 description 3
IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
UJMGZPCKYHBCKU-UHFFFAOYSA-N 2,2-dimethyl-2,3-dihydrobenzofuran Chemical compound C1=CC=C2OC(C)(C)CC2=C1 UJMGZPCKYHBCKU-UHFFFAOYSA-N 0.000 description 2
235000002566 Capsicum Nutrition 0.000 description 2
NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 description 2
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 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 2
230000003001 depressive effect Effects 0.000 description 2
150000005690 diesters Chemical class 0.000 description 2
238000004817 gas chromatography Methods 0.000 description 2
150000002431 hydrogen Chemical group 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
229920005610 lignin Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000004550 soluble concentrate Substances 0.000 description 2
230000000638 stimulation Effects 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
SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-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
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
ANHAEBWRQNIPEV-UHFFFAOYSA-N 2-chloroethyl dihydrogen phosphate Chemical compound OP(O)(=O)OCCCl ANHAEBWRQNIPEV-UHFFFAOYSA-N 0.000 description 1
WWOBYPKUYODHDG-UHFFFAOYSA-N 4-chlorocatechol Chemical compound OC1=CC=C(Cl)C=C1O WWOBYPKUYODHDG-UHFFFAOYSA-N 0.000 description 1
CFNMUZCFSDMZPQ-GHXNOFRVSA-N 7-[(z)-3-methyl-4-(4-methyl-5-oxo-2h-furan-2-yl)but-2-enoxy]chromen-2-one Chemical compound C=1C=C2C=CC(=O)OC2=CC=1OC/C=C(/C)CC1OC(=O)C(C)=C1 CFNMUZCFSDMZPQ-GHXNOFRVSA-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
240000008384 Capsicum annuum var. annuum Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
239000006002 Pepper Substances 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
241000722363 Piper Species 0.000 description 1
235000016761 Piper aduncum Nutrition 0.000 description 1
235000017804 Piper guineense Nutrition 0.000 description 1
235000008184 Piper nigrum 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
229920003171 Poly (ethylene oxide) Polymers 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
150000001346 alkyl aryl ethers Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000002238 attenuated effect Effects 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
238000004166 bioassay Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229940126543 compound 14 Drugs 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
125000004966 cyanoalkyl group Chemical group 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
230000000459 effect on growth Effects 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
229940067606 lecithin Drugs 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
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
230000035790 physiological processes and functions Effects 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000010088 rubber extraction Methods 0.000 description 1
CQRYARSYNCAZFO-UHFFFAOYSA-N salicyl alcohol Chemical compound OCC1=CC=CC=C1O CQRYARSYNCAZFO-UHFFFAOYSA-N 0.000 description 1
230000036555 skin type Effects 0.000 description 1
IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
230000007480 spreading Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
230000004936 stimulating effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000010408 sweeping Methods 0.000 description 1
150000007970 thio esters Chemical class 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
239000000080 wetting agent Substances 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)

CS855347A 1984-07-18 1985-07-18 Agent for plants growing regulation CS256391B2 (en)

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
CS256391B2 true CS256391B2 (en)	1988-04-15

Family

ID=10961156

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS855347A CS256391B2 (en)	1984-07-18	1985-07-18	Agent for plants growing regulation

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
HU190580B (en) *	1984-07-18	1986-09-29	Nitrokemia Ipartelepek,Hu	Plant growth regulating compositions comprising phosphonic acid-esters as active substance
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.

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2159364A (en) *		1939-05-23		Ethers of i
US4042370A (en) *	1974-09-18	1977-08-16	Sandoz Ltd.	Di-(acyloxyalkyl)-β-haloethane-phosphonates and dithiophosphonates and use as plant growth regulators
DD132632A1 (de) *	1977-08-12	1978-10-18	Bernhard Hesse	Mittel zur beeinflussung des pflanzenwachstums
DE2853936A1 (de) *	1978-12-14	1980-07-03	Bayer Ag	Phosphonsaeureester
GB2043072B (en) *	1979-02-13	1983-11-23	Symphar Sa	Diphosphonate compounds
GB2043073B (en) *	1979-02-13	1983-05-11	Symphar Sa	Mono-and diphosphonate compounds
DE3120437A1 (de) *	1981-05-22	1982-12-09	Hoechst Ag, 6000 Frankfurt	Verfahren zur herstellung von vinylphosphonsaeure
IL71373A (en) *	1983-04-07	1987-07-31	Mitsubishi Chem Ind	O-(2,3-dihydro-2,2-dimethyl-7 benzofuranyl)thiophosphoric and phosphonic esters,process for their production and pesticidal compositions containing them

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
DD239328A5 (de)	1986-09-24
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
RO94902A (fr)	1988-08-15
EP0188502A1 (fr)	1986-07-30
ES545631A0 (es)	1986-10-01

Publication	Publication Date	Title
SU803845A3 (ru)	1981-02-07	Гербицидный состав
EP0239414B1 (fr)	1989-11-02	Amide N-benzylique de l'acide 2-(4-fluoro-3-trifluorométhylphénoxy)butanoique et composition herbicide le contenant
EP0344533B1 (fr)	1993-12-08	Composition régulatrice de la croissance des plantes et procédé pour régler la croissance d'une plante
JP2606300B2 (ja)	1997-04-30	除草組成物
CS221820B2 (en)	1983-04-29	Herbicide means
US3518074A (en)	1970-06-30	Benzoylcholine halides as plant growth stunting agents
US2981619A (en)	1961-04-25	Method of inhibiting plant growth
US3332943A (en)	1967-07-25	Carbamoylthio derivatives
SU1486049A3 (ru)	1989-06-07	Способ регулирования роста сельскохозяйственных культур
US4023956A (en)	1977-05-17	Amide phosphorothiolate herbicides
US4398944A (en)	1983-08-16	Herbicidal composition and method for inhibiting growth of weeds
US4776874A (en)	1988-10-11	2-chloro-ethyl phosphonic acid esters and plant growth regulating agents containing same as active ingredient
RU2027715C1 (ru)	1995-01-27	Производное пиридинсульфонамида, обладающее гербицидной активностью
US3832155A (en)	1974-08-27	N-alkoxyalkylidenesulfonamide compounds as herbicides
KR100231518B1 (ko)	1999-11-15	농원예용살진균조성물
US4696947A (en)	1987-09-29	Nematocide
CA1047497A (fr)	1979-01-30	Derive heterocyclique
SU1111673A3 (ru)	1984-08-30	Способ борьбы с сорн ками
US3690865A (en)	1972-09-12	Method of combating unwanted vegetation in sugar beet fields
US4456471A (en)	1984-06-26	Herbicidal N-haloacetyl-2-methyl-6-substituted methoxymethylanilines
PL103650B1 (pl)	1979-07-31	Srodek owadobojczy,roztoczobojczy,nicieniobojczy i grzybobojczy
RU1826860C (ru)	1993-07-07	Гербицидна композици
DE2260763A1 (de)	1973-06-20	Mittel zum abtoeten von schaedlichen organismen
SU620193A3 (ru)	1978-08-15	Фунгицидное средство
US4486222A (en)	1984-12-04	Herbicide composition and process for the preparation of the active ingredients herbicidal phenyl carbonates