DD238910A5 - Pflanzenwachstumsregulierende mittel - Google Patents
Pflanzenwachstumsregulierende mittel Download PDFInfo
- Publication number
- DD238910A5 DD238910A5 DD85278589A DD27858985A DD238910A5 DD 238910 A5 DD238910 A5 DD 238910A5 DD 85278589 A DD85278589 A DD 85278589A DD 27858985 A DD27858985 A DD 27858985A DD 238910 A5 DD238910 A5 DD 238910A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- oxy
- plant growth
- dihydro
- dimethyl
- benzofuran
- Prior art date
Links
- -1 2,3-dihydro-2,2-dimethylbenzofuran-7-yl Chemical group 0.000 claims abstract description 30
- 239000004480 active ingredient Substances 0.000 claims abstract description 14
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 14
- 150000001768 cations Chemical class 0.000 claims abstract description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 2
- 230000008635 plant growth Effects 0.000 claims description 28
- 230000001105 regulatory effect Effects 0.000 claims description 15
- 239000002689 soil Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000000969 carrier Substances 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 238000011282 treatment Methods 0.000 description 41
- 150000001875 compounds Chemical class 0.000 description 37
- 241000196324 Embryophyta Species 0.000 description 26
- 230000000694 effects Effects 0.000 description 24
- 238000002360 preparation method Methods 0.000 description 23
- 239000000203 mixture Substances 0.000 description 20
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 18
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 17
- 240000003768 Solanum lycopersicum Species 0.000 description 17
- MSHBKNAWDRSOSF-UHFFFAOYSA-N 7-(2-diethoxyphosphorylethoxy)-2,2-dimethyl-3h-1-benzofuran Chemical compound CCOP(=O)(OCC)CCOC1=CC=CC2=C1OC(C)(C)C2 MSHBKNAWDRSOSF-UHFFFAOYSA-N 0.000 description 16
- 244000068988 Glycine max Species 0.000 description 16
- 235000010469 Glycine max Nutrition 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- HSHNITRMYYLLCV-UHFFFAOYSA-N 4-methylumbelliferone Chemical compound C1=C(O)C=CC2=C1OC(=O)C=C2C HSHNITRMYYLLCV-UHFFFAOYSA-N 0.000 description 14
- 230000012010 growth Effects 0.000 description 14
- 238000012360 testing method Methods 0.000 description 12
- 235000003222 Helianthus annuus Nutrition 0.000 description 11
- 230000008859 change Effects 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- JSTAJDYYTGMGEN-UHFFFAOYSA-N 2-(4-methyl-2-oxochromen-7-yl)oxyethylphosphonic acid Chemical compound CC1=CC(OC2=CC(=CC=C12)OCCP(O)(O)=O)=O JSTAJDYYTGMGEN-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 8
- 239000007921 spray Substances 0.000 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 description 7
- 241000209140 Triticum Species 0.000 description 7
- 235000021307 Triticum Nutrition 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- 244000020551 Helianthus annuus Species 0.000 description 6
- 230000002829 reductive effect Effects 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 241000208818 Helianthus Species 0.000 description 5
- 239000004495 emulsifiable concentrate Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000005292 vacuum distillation Methods 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
- RWQJSKNITXLYII-UHFFFAOYSA-N 7-(2-diethoxyphosphorylethoxy)-4-methylchromen-2-one Chemical compound CC1=CC(=O)OC2=CC(OCCP(=O)(OCC)OCC)=CC=C21 RWQJSKNITXLYII-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- 239000003444 phase transfer catalyst Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000001603 reducing effect Effects 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-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
- 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
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- AZKCXBXKASIJBY-OWOJBTEDSA-N [(E)-2-chloroethenyl]phosphonic acid Chemical compound Cl/C=C/P(O)(O)=O AZKCXBXKASIJBY-OWOJBTEDSA-N 0.000 description 3
- 239000001511 capsicum annuum Substances 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 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
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 235000013599 spices Nutrition 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- IBYHHJPAARCAIE-UHFFFAOYSA-N 1-bromo-2-chloroethane Chemical compound ClCCBr IBYHHJPAARCAIE-UHFFFAOYSA-N 0.000 description 2
- XLLJFWFFIDCGMI-UHFFFAOYSA-N 7-(2-bromoethoxy)-4-methylchromen-2-one Chemical compound C1=C(OCCBr)C=CC2=C1OC(=O)C=C2C XLLJFWFFIDCGMI-UHFFFAOYSA-N 0.000 description 2
- ZMBGUZNIPBCBMC-UHFFFAOYSA-N 7-(2-chloroethoxy)-2,2-dimethyl-3h-1-benzofuran Chemical compound C1=CC(OCCCl)=C2OC(C)(C)CC2=C1 ZMBGUZNIPBCBMC-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 239000006002 Pepper Substances 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical group 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- VJGNLOIQCWLBJR-UHFFFAOYSA-M benzyl(tributyl)azanium;chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CC1=CC=CC=C1 VJGNLOIQCWLBJR-UHFFFAOYSA-M 0.000 description 2
- YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000000843 powder Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000002426 superphosphate Substances 0.000 description 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- JNFBOWNNNAHVNZ-UHFFFAOYSA-N 1,2-dibromoethyne Chemical compound BrC#CBr JNFBOWNNNAHVNZ-UHFFFAOYSA-N 0.000 description 1
- JJOHSFWZFCGFNT-UHFFFAOYSA-N 1-(4-bromo-3-chlorophenyl)-3-methoxy-1-methylurea Chemical compound CONC(=O)N(C)C1=CC=C(Br)C(Cl)=C1 JJOHSFWZFCGFNT-UHFFFAOYSA-N 0.000 description 1
- OLKWMFUGWXLVNM-UHFFFAOYSA-N 2,2,4-trimethylchromen-7-ol Chemical compound OC1=CC=C2C(C)=CC(C)(C)OC2=C1 OLKWMFUGWXLVNM-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
- XPIQJMUYUKAKNX-VOTSOKGWSA-N 3-[(2e)-octa-2,7-dienyl]oxolane-2,5-dione Chemical class C=CCCC\C=C\CC1CC(=O)OC1=O XPIQJMUYUKAKNX-VOTSOKGWSA-N 0.000 description 1
- WZHMHOPKMPGQLO-UHFFFAOYSA-N 3-hydroxy-4-methylchromen-2-one Chemical compound C1=CC=CC2=C1OC(=O)C(O)=C2C WZHMHOPKMPGQLO-UHFFFAOYSA-N 0.000 description 1
- HKLGDJFRTRDDGE-UHFFFAOYSA-N 4-methyl-3h-chromene-2,7-dione Chemical compound C1=CC(=O)C=C2OC(=O)CC(C)=C21 HKLGDJFRTRDDGE-UHFFFAOYSA-N 0.000 description 1
- CSBLCDBHJJXRBX-UHFFFAOYSA-N 7-[2-[bis(2-chloroethoxy)phosphoryl]ethoxy]-2,2-dimethyl-3h-1-benzofuran Chemical compound C1=CC(OCCP(=O)(OCCCl)OCCCl)=C2OC(C)(C)CC2=C1 CSBLCDBHJJXRBX-UHFFFAOYSA-N 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 229930192334 Auxin Natural products 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- GHMDBLDLEYKYOS-UHFFFAOYSA-N CC1(CC2=C(O1)C(=CC=C2)OCCP(=O)(OCCOC)OCCOC)C Chemical compound CC1(CC2=C(O1)C(=CC=C2)OCCP(=O)(OCCOC)OCCOC)C GHMDBLDLEYKYOS-UHFFFAOYSA-N 0.000 description 1
- NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-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
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 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
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000002363 auxin Substances 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
- 210000004556 brain Anatomy 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229950005434 chloropyrilene Drugs 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000004720 fertilization Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003895 organic fertilizer Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 125000005342 perphosphate group Chemical group 0.000 description 1
- 230000004526 pharmaceutical effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012261 resinous substance Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 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
- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU842801A HU190580B (en) | 1984-07-18 | 1984-07-18 | Plant growth regulating compositions comprising phosphonic acid-esters as active substance |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD238910A5 true DD238910A5 (de) | 1986-09-10 |
Family
ID=10961160
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD85278589A DD238910A5 (de) | 1984-07-18 | 1985-07-15 | Pflanzenwachstumsregulierende mittel |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4776874A (es) |
| EP (1) | EP0187806A1 (es) |
| JP (1) | JPS61502754A (es) |
| BG (1) | BG47499A3 (es) |
| CS (1) | CS259882B2 (es) |
| DD (1) | DD238910A5 (es) |
| DK (1) | DK123986A (es) |
| ES (1) | ES8706708A1 (es) |
| HU (1) | HU190580B (es) |
| WO (1) | WO1986000903A1 (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2011349461A1 (en) | 2010-12-21 | 2013-06-27 | Bayer Cropscience Lp | Sandpaper mutants of Bacillus and methods of their use to enhance plant growth, promote plant health and control diseases and pests |
| BR112014005654A2 (pt) | 2011-09-12 | 2017-03-28 | Bayer Cropscience Lp | métodos para melhorar a saúde e promover o crescimento de uma planta e/ou de melhorar o amadurecimento da fruta |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3531549A (en) * | 1967-02-23 | 1970-09-29 | Gaf Corp | Catechol half esters of beta-haloethylphosphonic acid |
| US3551528A (en) * | 1967-02-23 | 1970-12-29 | Gaf Corp | Phosphonic acid esters and the methol for their preparation |
| US4042370A (en) * | 1974-09-18 | 1977-08-16 | Sandoz Ltd. | Di-(acyloxyalkyl)-β-haloethane-phosphonates and dithiophosphonates and use as plant growth regulators |
| US4172863A (en) * | 1976-06-14 | 1979-10-30 | Waldmann John J | Halogen-containing phosphates |
| CA1085870A (en) * | 1976-12-20 | 1980-09-16 | Robert J. Kiesel | Preparation of haloalylphosphonic acid |
| DD132632A1 (de) * | 1977-08-12 | 1978-10-18 | Bernhard Hesse | Mittel zur beeinflussung des pflanzenwachstums |
| DE3001895A1 (de) * | 1980-01-19 | 1981-07-23 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von alkanphosphonsaeurediarylester und alkanphosphinsaeurearylestern |
| 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 |
| HU190579B (en) * | 1984-07-18 | 1986-09-29 | Nitrokemia Ipartelepek,Hu | Plant growth regulating compositions comprising etherified hydroxy-alkyl-phosphonic acid-derivatives as active substance |
-
1984
- 1984-07-18 HU HU842801A patent/HU190580B/hu not_active IP Right Cessation
-
1985
- 1985-07-12 JP JP60503199A patent/JPS61502754A/ja active Pending
- 1985-07-12 WO PCT/HU1985/000043 patent/WO1986000903A1/en not_active Application Discontinuation
- 1985-07-12 EP EP85903354A patent/EP0187806A1/en not_active Ceased
- 1985-07-15 DD DD85278589A patent/DD238910A5/de unknown
- 1985-07-17 US US06/839,498 patent/US4776874A/en not_active Expired - Fee Related
- 1985-07-18 ES ES545632A patent/ES8706708A1/es not_active Expired
- 1985-07-18 CS CS855348A patent/CS259882B2/cs unknown
-
1986
- 1986-03-18 BG BG074116A patent/BG47499A3/xx unknown
- 1986-03-18 DK DK123986A patent/DK123986A/da not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ES8706708A1 (es) | 1987-07-01 |
| CS534885A2 (en) | 1988-03-15 |
| WO1986000903A1 (en) | 1986-02-13 |
| JPS61502754A (ja) | 1986-11-27 |
| HU190580B (en) | 1986-09-29 |
| BG47499A3 (en) | 1990-07-16 |
| US4776874A (en) | 1988-10-11 |
| EP0187806A1 (en) | 1986-07-23 |
| CS259882B2 (en) | 1988-11-15 |
| DK123986D0 (da) | 1986-03-18 |
| ES545632A0 (es) | 1987-07-01 |
| DK123986A (da) | 1986-03-18 |
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