LV10992B - 4- phenoxycoumarins as herbicidal agents - Google Patents

4- phenoxycoumarins as herbicidal agents Download PDF

Info

Publication number: LV10992B
Authority: LV; Latvia
Prior art keywords: alkyl; dichlorophenoxy; halogen; haloalkyl; optionally substituted
Prior art date: 1994-07-25

Application number

LVP-95-226A

Other languages

English (en)

Latvian (lv)

Other versions

LV10992A (lv

Inventor

Sergio I Alvarado

Pierre Antoine Marc

Brian J Dahlke

Eileen M Reilly

Original Assignee

American Cyanamid Co

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.)

1994-07-25

Filing date

1995-07-25

Publication date

1996-06-20

1995-07-25 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1996-02-20 Publication of LV10992A publication Critical patent/LV10992A/xx

1996-06-20 Publication of LV10992B publication Critical patent/LV10992B/en

Links

239000004009 herbicide Substances 0.000 title claims description 9
CPERZDRUHMSAMP-UHFFFAOYSA-N 4-phenoxychromen-2-one Chemical class C12=CC=CC=C2OC(=O)C=C1OC1=CC=CC=C1 CPERZDRUHMSAMP-UHFFFAOYSA-N 0.000 title description 7
229910052736 halogen Inorganic materials 0.000 claims description 66
150000002367 halogens Chemical class 0.000 claims description 65
125000000217 alkyl group Chemical group 0.000 claims description 57
-1 2,6-Dichlorophenoxy Chemical group 0.000 claims description 50
150000001875 compounds Chemical class 0.000 claims description 43
241000196324 Embryophyta Species 0.000 claims description 34
125000003545 alkoxy group Chemical group 0.000 claims description 33
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims description 29
125000001188 haloalkyl group Chemical group 0.000 claims description 29
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 28
238000000034 method Methods 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 24
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 24
238000002360 preparation method Methods 0.000 claims description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 20
240000007594 Oryza sativa Species 0.000 claims description 19
125000001424 substituent group Chemical group 0.000 claims description 19
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 18
230000002363 herbicidal effect Effects 0.000 claims description 18
229960000956 coumarin Drugs 0.000 claims description 17
229910052739 hydrogen Inorganic materials 0.000 claims description 17
239000002689 soil Substances 0.000 claims description 17
235000007164 Oryza sativa Nutrition 0.000 claims description 15
235000001671 coumarin Nutrition 0.000 claims description 15
235000009566 rice Nutrition 0.000 claims description 15
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 14
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 11
125000003342 alkenyl group Chemical group 0.000 claims description 11
125000000262 haloalkenyl group Chemical group 0.000 claims description 11
125000000232 haloalkynyl group Chemical group 0.000 claims description 11
229910052760 oxygen Inorganic materials 0.000 claims description 11
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 10
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 9
125000000753 cycloalkyl group Chemical group 0.000 claims description 9
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 7
239000001301 oxygen Substances 0.000 claims description 7
TUWDFRJHLFOUMI-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-5-nitrochromen-2-one Chemical compound C1=2C([N+](=O)[O-])=CC=CC=2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl TUWDFRJHLFOUMI-UHFFFAOYSA-N 0.000 claims description 6
125000004429 atom Chemical group 0.000 claims description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
OQMNHMKKIYYCCH-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-5-methylchromen-2-one Chemical compound C1=2C(C)=CC=CC=2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl OQMNHMKKIYYCCH-UHFFFAOYSA-N 0.000 claims description 5
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
240000005979 Hordeum vulgare Species 0.000 claims description 5
235000007340 Hordeum vulgare Nutrition 0.000 claims description 5
241000209056 Secale Species 0.000 claims description 5
235000007238 Secale cereale Nutrition 0.000 claims description 5
241000209140 Triticum Species 0.000 claims description 5
235000021307 Triticum Nutrition 0.000 claims description 5
240000008042 Zea mays Species 0.000 claims description 5
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
239000002904 solvent Substances 0.000 claims description 3
235000007319 Avena orientalis Nutrition 0.000 claims description 2
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 20
239000001257 hydrogen Substances 0.000 claims 14
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 14
125000004093 cyano group Chemical group *C#N 0.000 claims 12
125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
210000000056 organ Anatomy 0.000 claims 2
230000001850 reproductive effect Effects 0.000 claims 2
244000075850 Avena orientalis Species 0.000 claims 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims 1
230000008878 coupling Effects 0.000 claims 1
238000010168 coupling process Methods 0.000 claims 1
238000005859 coupling reaction Methods 0.000 claims 1
235000009973 maize Nutrition 0.000 claims 1
150000002926 oxygen Chemical class 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 27
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 21
238000011156 evaluation Methods 0.000 description 19
239000000047 product Substances 0.000 description 19
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
238000004458 analytical method Methods 0.000 description 12
235000013339 cereals Nutrition 0.000 description 12
239000007787 solid Substances 0.000 description 11
239000000243 solution Substances 0.000 description 11
230000003595 spectral effect Effects 0.000 description 11
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
239000012065 filter cake Substances 0.000 description 9
125000004438 haloalkoxy group Chemical group 0.000 description 9
244000038559 crop plants Species 0.000 description 8
238000010586 diagram Methods 0.000 description 8
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
229910052799 carbon Inorganic materials 0.000 description 7
238000010992 reflux Methods 0.000 description 7
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 6
238000012272 crop production Methods 0.000 description 6
230000006378 damage Effects 0.000 description 6
238000004128 high performance liquid chromatography Methods 0.000 description 6
239000005457 ice water Substances 0.000 description 6
229910000104 sodium hydride Inorganic materials 0.000 description 6
KFQPNUQMBBQQPH-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-6-methoxychromen-2-one Chemical compound C12=CC(OC)=CC=C2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl KFQPNUQMBBQQPH-UHFFFAOYSA-N 0.000 description 5
125000004414 alkyl thio group Chemical group 0.000 description 5
125000000304 alkynyl group Chemical group 0.000 description 5
230000001902 propagating effect Effects 0.000 description 5
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 4
238000005160 1H NMR spectroscopy Methods 0.000 description 4
MJKVTPMWOKAVMS-UHFFFAOYSA-N 3-hydroxy-1-benzopyran-2-one Chemical compound C1=CC=C2OC(=O)C(O)=CC2=C1 MJKVTPMWOKAVMS-UHFFFAOYSA-N 0.000 description 4
LVCHHJGAUZYEIG-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-5,6,7-trimethoxychromen-2-one Chemical compound C1=2C(OC)=C(OC)C(OC)=CC=2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl LVCHHJGAUZYEIG-UHFFFAOYSA-N 0.000 description 4
LEZRENZRQRVEOA-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-6,7-dimethoxychromen-2-one Chemical compound C1=2C=C(OC)C(OC)=CC=2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl LEZRENZRQRVEOA-UHFFFAOYSA-N 0.000 description 4
VXIXUWQIVKSKSA-UHFFFAOYSA-N 4-hydroxycoumarin Chemical compound C1=CC=CC2=C1OC(=O)C=C2O VXIXUWQIVKSKSA-UHFFFAOYSA-N 0.000 description 4
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 4
208000027418 Wounds and injury Diseases 0.000 description 4
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
229910052794 bromium Inorganic materials 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
235000005822 corn Nutrition 0.000 description 4
230000000694 effects Effects 0.000 description 4
208000014674 injury Diseases 0.000 description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
239000012071 phase Substances 0.000 description 4
230000000885 phytotoxic effect Effects 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000011369 resultant mixture Substances 0.000 description 4
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
239000012258 stirred mixture Substances 0.000 description 4
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
TZNUKOCBYXFUQE-UHFFFAOYSA-N 3-phenoxychromen-2-one Chemical class O=C1OC=2C=CC=CC=2C=C1OC1=CC=CC=C1 TZNUKOCBYXFUQE-UHFFFAOYSA-N 0.000 description 3
KYURQUUDMGNXPQ-UHFFFAOYSA-N 4-(2,6-dibromophenoxy)-5,6,7-trimethoxychromen-2-one Chemical compound C1=2C(OC)=C(OC)C(OC)=CC=2OC(=O)C=C1OC1=C(Br)C=CC=C1Br KYURQUUDMGNXPQ-UHFFFAOYSA-N 0.000 description 3
ZFPUBWWKAHUWBZ-UHFFFAOYSA-N 4-(2,6-dibromophenoxy)-5-(trifluoromethyl)chromen-2-one Chemical compound C1=2C(C(F)(F)F)=CC=CC=2OC(=O)C=C1OC1=C(Br)C=CC=C1Br ZFPUBWWKAHUWBZ-UHFFFAOYSA-N 0.000 description 3
AAKGOIDCJDRTRO-UHFFFAOYSA-N 4-(2,6-dibromophenoxy)-8-methoxychromen-2-one Chemical compound C=1C(=O)OC=2C(OC)=CC=CC=2C=1OC1=C(Br)C=CC=C1Br AAKGOIDCJDRTRO-UHFFFAOYSA-N 0.000 description 3
PXUUIKKCUMPFHT-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-5-(trifluoromethyl)chromen-2-one Chemical compound C1=2C(C(F)(F)F)=CC=CC=2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl PXUUIKKCUMPFHT-UHFFFAOYSA-N 0.000 description 3
VCVNVJSZBZOWAH-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-5-fluorochromen-2-one Chemical compound C1=2C(F)=CC=CC=2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl VCVNVJSZBZOWAH-UHFFFAOYSA-N 0.000 description 3
IVKXSLHSMHUYHP-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-6-hydroxychromen-2-one Chemical compound C12=CC(O)=CC=C2OC(=O)C=C1OC1=C(Cl)C=CC=C1Cl IVKXSLHSMHUYHP-UHFFFAOYSA-N 0.000 description 3
HIVWHNGWXSLBLX-UHFFFAOYSA-N 5-chloro-4-(2,6-dibromophenoxy)chromen-2-one Chemical compound C1=2C(Cl)=CC=CC=2OC(=O)C=C1OC1=C(Br)C=CC=C1Br HIVWHNGWXSLBLX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
241000722731 Carex Species 0.000 description 3
244000058871 Echinochloa crus-galli Species 0.000 description 3
101100134929 Gallus gallus COR9 gene Proteins 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
235000003990 Monochoria hastata Nutrition 0.000 description 3
240000000178 Monochoria vaginalis Species 0.000 description 3
241000209504 Poaceae Species 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
241001148683 Zostera marina Species 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
239000012267 brine Substances 0.000 description 3
238000004587 chromatography analysis Methods 0.000 description 3
239000013078 crystal Substances 0.000 description 3
238000000921 elemental analysis Methods 0.000 description 3
239000000284 extract Substances 0.000 description 3
239000000706 filtrate Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
SMFFZOQLHYIRDA-UHFFFAOYSA-N 3,4-dimethoxyphenol Chemical compound COC1=CC=C(O)C=C1OC SMFFZOQLHYIRDA-UHFFFAOYSA-N 0.000 description 2
CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
CKCOPMSBJBNBCQ-UHFFFAOYSA-N 3-chlorochromen-2-one Chemical compound C1=CC=C2OC(=O)C(Cl)=CC2=C1 CKCOPMSBJBNBCQ-UHFFFAOYSA-N 0.000 description 2
AUZQQIPZESHNMG-UHFFFAOYSA-N 3-methoxysalicylic acid Chemical compound COC1=CC=CC(C(O)=O)=C1O AUZQQIPZESHNMG-UHFFFAOYSA-N 0.000 description 2
QQXMYPKDCLLTEX-UHFFFAOYSA-N 4-(2,6-dichlorophenoxy)-8-methoxychromen-2-one Chemical compound C=1C(=O)OC=2C(OC)=CC=CC=2C=1OC1=C(Cl)C=CC=C1Cl QQXMYPKDCLLTEX-UHFFFAOYSA-N 0.000 description 2
RKEYJFRSDLEQIE-UHFFFAOYSA-N 4-chlorochromen-2-one Chemical class C1=CC=CC2=C1OC(=O)C=C2Cl RKEYJFRSDLEQIE-UHFFFAOYSA-N 0.000 description 2
VRZRUMKBZIBSMP-UHFFFAOYSA-N 5-chloro-4-(2,6-dichlorophenoxy)chromen-2-one Chemical compound ClC1=CC=CC(Cl)=C1OC1=CC(=O)OC2=C1C(Cl)=CC=C2 VRZRUMKBZIBSMP-UHFFFAOYSA-N 0.000 description 2
KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 2
125000004399 C1-C4 alkenyl group Chemical group 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
235000002848 Cyperus flabelliformis Nutrition 0.000 description 2
240000001505 Cyperus odoratus Species 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
241000192043 Echinochloa Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
229940100389 Sulfonylurea Drugs 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
235000011089 carbon dioxide Nutrition 0.000 description 2
238000001816 cooling Methods 0.000 description 2
VHILMKFSCRWWIJ-UHFFFAOYSA-N dimethyl acetylenedicarboxylate Chemical compound COC(=O)C#CC(=O)OC VHILMKFSCRWWIJ-UHFFFAOYSA-N 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000001530 fumaric acid Substances 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229940098779 methanesulfonic acid Drugs 0.000 description 2
DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical compound CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 2
LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
230000002085 persistent effect Effects 0.000 description 2
231100000208 phytotoxic Toxicity 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
229960004889 salicylic acid Drugs 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000012312 sodium hydride Substances 0.000 description 2
OJXASOYYODXRPT-UHFFFAOYSA-N sulfamoylurea Chemical compound NC(=O)NS(N)(=O)=O OJXASOYYODXRPT-UHFFFAOYSA-N 0.000 description 2
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical compound OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 2
DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
ZOVFLKOKOZVLQC-UHFFFAOYSA-N thiochromene-2-thione Chemical compound C1=CC=C2SC(=S)C=CC2=C1 ZOVFLKOKOZVLQC-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
CICJCOXCUHHCJY-YVMONPNESA-N (z)-2-[4-(trifluoromethoxy)phenoxy]but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)/OC1=CC=C(OC(F)(F)F)C=C1 CICJCOXCUHHCJY-YVMONPNESA-N 0.000 description 1
IYMYYQMPOBPRPU-UHFFFAOYSA-N 1-[2-fluoro-6-(trifluoromethyl)phenyl]ethanone Chemical compound CC(=O)C1=C(F)C=CC=C1C(F)(F)F IYMYYQMPOBPRPU-UHFFFAOYSA-N 0.000 description 1
LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
HOLHYSJJBXSLMV-UHFFFAOYSA-N 2,6-dichlorophenol Chemical compound OC1=C(Cl)C=CC=C1Cl HOLHYSJJBXSLMV-UHFFFAOYSA-N 0.000 description 1
QRDSMOKYRCJBDG-UHFFFAOYSA-N 2-(dichloromethyl)-6-nitrophenol Chemical compound OC1=C(C(Cl)Cl)C=CC=C1[N+]([O-])=O QRDSMOKYRCJBDG-UHFFFAOYSA-N 0.000 description 1
ZWVHTXAYIKBMEE-UHFFFAOYSA-N 2-hydroxyacetophenone Chemical class OCC(=O)C1=CC=CC=C1 ZWVHTXAYIKBMEE-UHFFFAOYSA-N 0.000 description 1
LZEYBPBDKIHNRL-UHFFFAOYSA-N 4-(2,6-dibromophenoxy)-6,7-dimethoxychromen-2-one Chemical compound C1=2C=C(OC)C(OC)=CC=2OC(=O)C=C1OC1=C(Br)C=CC=C1Br LZEYBPBDKIHNRL-UHFFFAOYSA-N 0.000 description 1
WDRJNKMAZMEYOF-UHFFFAOYSA-N 4-(trifluoromethoxy)phenol Chemical compound OC1=CC=C(OC(F)(F)F)C=C1 WDRJNKMAZMEYOF-UHFFFAOYSA-N 0.000 description 1
GNYUIFAQVWIXJS-UHFFFAOYSA-N 4-chloro-6-methoxychromen-2-one Chemical compound O1C(=O)C=C(Cl)C2=CC(OC)=CC=C21 GNYUIFAQVWIXJS-UHFFFAOYSA-N 0.000 description 1
KFXXRRQBVLINPH-UHFFFAOYSA-N 4-hydroxy-6-methoxychromen-2-one Chemical compound O1C(=O)C=C(O)C2=CC(OC)=CC=C21 KFXXRRQBVLINPH-UHFFFAOYSA-N 0.000 description 1
RVMGXWBCQGAWBR-UHFFFAOYSA-N 4-oxo-1-benzopyran-2-carboxylic acid Chemical compound C1=CC=C2OC(C(=O)O)=CC(=O)C2=C1 RVMGXWBCQGAWBR-UHFFFAOYSA-N 0.000 description 1
OPSSGAQQBKUUGE-UHFFFAOYSA-N 4-oxo-6-(trifluoromethoxy)chromene-2-carboxylic acid Chemical compound FC(F)(F)OC1=CC=C2OC(C(=O)O)=CC(=O)C2=C1 OPSSGAQQBKUUGE-UHFFFAOYSA-N 0.000 description 1
ZXGMMHMAGOAFGQ-UHFFFAOYSA-N 6-methyl-3-oxa-13-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2(7),8-trien-4-one Chemical compound C1CCN2CCCC3=C2C1=C1OC(=O)CC(C)C1=C3 ZXGMMHMAGOAFGQ-UHFFFAOYSA-N 0.000 description 1
241000209763 Avena sativa Species 0.000 description 1
235000007558 Avena sp Nutrition 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
244000150187 Cyperus papyrus Species 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000169139 Monochoria Species 0.000 description 1
YZAJGNMSFKRIGI-UHFFFAOYSA-N N1C(S(=O)(=O)N)=NC=C2N=CC=C21 Chemical compound N1C(S(=O)(=O)N)=NC=C2N=CC=C21 YZAJGNMSFKRIGI-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
235000019502 Orange oil Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
235000005324 Typha latifolia Nutrition 0.000 description 1
241000208041 Veronica Species 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
230000009418 agronomic effect Effects 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
150000004775 coumarins Chemical class 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000002024 ethyl acetate extract Substances 0.000 description 1
UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
208000006278 hypochromic anemia Diseases 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
230000036244 malformation Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000010907 mechanical stirring Methods 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
239000010502 orange oil Substances 0.000 description 1
238000003359 percent control normalization Methods 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000002243 precursor Substances 0.000 description 1
230000035755 proliferation Effects 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
239000012217 radiopharmaceutical Substances 0.000 description 1
229940121896 radiopharmaceutical Drugs 0.000 description 1
230000002799 radiopharmaceutical effect Effects 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
230000000007 visual effect Effects 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/18—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with sulfur as the ring hetero atom
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/42—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4
- C07D311/44—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 with one hydrogen atom in position 3
- C07D311/46—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 with one hydrogen atom in position 3 unsubstituted in the carbocyclic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/42—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4
- C07D311/44—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 with one hydrogen atom in position 3
- C07D311/54—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 with one hydrogen atom in position 3 substituted in the carbocyclic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/04—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D335/06—Benzothiopyrans; Hydrogenated benzothiopyrans

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plural Heterocyclic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pyrane Compounds (AREA)
Heterocyclic Compounds Containing Sulfur Atoms (AREA)

LVP-95-226A 1994-07-25 1995-07-25 4- phenoxycoumarins as herbicidal agents LV10992B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US08/279,579 US5563280A (en)	1994-07-25	1994-07-25	4-Phenoxycoumarins as herbicidal agents

Publications (2)

Publication Number	Publication Date
LV10992A LV10992A (lv)	1996-02-20
LV10992B true LV10992B (en)	1996-06-20

Family

ID=23069573

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LVP-95-226A LV10992B (en)	1994-07-25	1995-07-25	4- phenoxycoumarins as herbicidal agents

Country Status (23)

Country	Link
US (3)	US5563280A (cs)
EP (1)	EP0694257A1 (cs)
JP (1)	JPH0873304A (cs)
KR (1)	KR960003574A (cs)
CN (1)	CN1119188A (cs)
AU (1)	AU2715195A (cs)
BR (1)	BR9503417A (cs)
CA (1)	CA2154408A1 (cs)
CZ (1)	CZ183195A3 (cs)
EE (1)	EE9500030A (cs)
HU (1)	HUT75945A (cs)
IL (1)	IL114704A0 (cs)
LV (1)	LV10992B (cs)
MD (1)	MD950364A (cs)
NO (1)	NO952940L (cs)
NZ (1)	NZ272626A (cs)
PL (1)	PL309764A1 (cs)
RU (1)	RU95113207A (cs)
SK (1)	SK92995A3 (cs)
TJ (1)	TJ95000241A (cs)
TR (1)	TR199500890A2 (cs)
TW (1)	TW318846B (cs)
ZA (1)	ZA956151B (cs)

Cited By (1)

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CN106749144A (zh) *	2016-12-27	2017-05-31	江苏大学	7‑芳氧乙酰氧基香豆素类化合物及其在农药上的应用

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US5808105A (en) *	1995-10-10	1998-09-15	American Cyanamid Company	4-phenoxycoumarins as herbicidal agents
EP0861242B1 (en) *	1995-10-13	2001-05-30	Aventis CropScience UK Limited	Heterocyclic fungicides
CA2433578A1 (en) *	2000-12-28	2002-07-11	Koichi Niimura	Process for preparation of esculetin compounds, esculetin compounds and intermediates thereof, and use of both
EP1504000A4 (en) *	2002-05-14	2006-08-23	Vivoquest Inc	4-THIO COUMARINES
US7148253B2 (en) *	2002-05-14	2006-12-12	Xtl Biopharmaceuticals Ltd.	4-thio coumarins
HRP20030603A2 (en)	2003-07-25	2005-10-31	Pliva-Istra�iva�ki institut d.o.o.	Substituted furochromene compounds of antiinflammatory action
CN100405907C (zh) *	2005-11-18	2008-07-30	党永富	一种除草剂安全添加剂
CA2657093A1 (en) *	2006-07-07	2008-01-10	Steven P. Govek	Bicyclic heteroaryl inhibitors of pde4
US8338337B2 (en) *	2008-10-29	2012-12-25	Basf Se	Substituted pyridines having a herbicidal effect
BRPI1008214A2 (pt) *	2009-06-05	2015-08-25	Basf Se	"composto de pirazina da fórmula i, composto da fórmula i, processo para preparar o composto da fórmula i, composição e método para controlar uma vegetação indesejável"
CN104592183B (zh) *	2015-01-15	2016-05-18	青岛农业大学	N-酰基-n-间氟苄基-8-氨基香豆素类化合物及其制备与除草用途
CN109293616B (zh) *	2018-09-29	2022-06-21	贵州大学	一种含香豆素查尔酮类衍生物、其制备方法及应用
CN112806361B (zh) *	2019-11-18	2021-12-24	党永富	炭吸附4-羟基香豆素除草剂安全添加剂及其在治理除草剂副作用中的应用
KR102734863B1 (ko) *	2022-05-27	2024-11-29	엘림영농조합법인	복령의 재배방법
CN118290379A (zh) *	2024-03-19	2024-07-05	贵州工业职业技术学院	一种新型农用多功能物质的制备方法及其在抗病毒、抑菌以及促进植物生长方面的应用

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HU192678B (en) *	1985-03-04	1987-06-29	Nitrokemia Ipartelepek	Composition and process for treating field plants
IL85347A0 (en) *	1987-02-11	1988-07-31	May & Baker Ltd	Cyclic diones
GB2207425A (en) *	1987-07-30	1989-02-01	Shell Int Research	Diphenyl ether herbicides
DE3810706A1 (de) *	1988-03-25	1989-10-05	Schering Ag	Substituierte cumarinderivate, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider wirkung
JPH03227923A (ja) *	1990-01-30	1991-10-08	Sawai Seiyaku Kk	ひと免疫不全ウイルス疾患処置剤
HUT63843A (en) *	1992-02-13	1993-10-28	Biosignal Kutato Fejlesztoe Kf	Process for producing new kumarin derivatives and their analogs inhibiting mammal cell proliferation and tumour growth, as well as pharmaceutical comkpositions comprising such compounds

1994
- 1994-07-25 US US08/279,579 patent/US5563280A/en not_active Expired - Lifetime
1995
- 1995-07-14 CZ CZ951831A patent/CZ183195A3/cs unknown
- 1995-07-19 TW TW084107484A patent/TW318846B/zh active
- 1995-07-21 CA CA002154408A patent/CA2154408A1/en not_active Abandoned
- 1995-07-21 SK SK929-95A patent/SK92995A3/sk unknown
- 1995-07-21 TR TR95/00890A patent/TR199500890A2/xx unknown
- 1995-07-21 EP EP95305098A patent/EP0694257A1/en not_active Ceased
- 1995-07-24 AU AU27151/95A patent/AU2715195A/en not_active Abandoned
- 1995-07-24 IL IL11470495A patent/IL114704A0/xx unknown
- 1995-07-24 EE EE9500030A patent/EE9500030A/xx unknown
- 1995-07-24 NZ NZ272626A patent/NZ272626A/en unknown
- 1995-07-24 MD MD95-0364A patent/MD950364A/ro not_active Application Discontinuation
- 1995-07-24 RU RU95113207/04A patent/RU95113207A/ru unknown
- 1995-07-24 ZA ZA956151A patent/ZA956151B/xx unknown
- 1995-07-24 TJ TJ95000241A patent/TJ95000241A/xx unknown
- 1995-07-24 NO NO952940A patent/NO952940L/no unknown
- 1995-07-24 BR BR9503417A patent/BR9503417A/pt not_active Application Discontinuation
- 1995-07-24 HU HU9502218A patent/HUT75945A/hu unknown
- 1995-07-24 KR KR1019950021891A patent/KR960003574A/ko not_active Ceased
- 1995-07-24 JP JP7208342A patent/JPH0873304A/ja active Pending
- 1995-07-25 LV LVP-95-226A patent/LV10992B/en unknown
- 1995-07-25 PL PL95309764A patent/PL309764A1/xx unknown
- 1995-07-25 CN CN95107592A patent/CN1119188A/zh active Pending
- 1995-10-10 US US08/515,846 patent/US5681968A/en not_active Expired - Fee Related
1997
- 1997-03-21 US US08/821,900 patent/US5759959A/en not_active Expired - Fee Related

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN106749144A (zh) *	2016-12-27	2017-05-31	江苏大学	7‑芳氧乙酰氧基香豆素类化合物及其在农药上的应用
CN106749144B (zh) *	2016-12-27	2019-06-28	江苏大学	7-芳氧乙酰氧基香豆素类化合物及其在农药上的应用

Also Published As

Publication number	Publication date
US5681968A (en)	1997-10-28
NZ272626A (en)	1997-06-24
CA2154408A1 (en)	1996-01-26
MD950364A (ro)	1997-01-31
TW318846B (cs)	1997-11-01
EP0694257A1 (en)	1996-01-31
US5563280A (en)	1996-10-08
SK92995A3 (en)	1996-02-07
EE9500030A (et)	1996-02-15
RU95113207A (ru)	1997-06-27
HU9502218D0 (en)	1995-09-28
NO952940D0 (no)	1995-07-24
LV10992A (lv)	1996-02-20
JPH0873304A (ja)	1996-03-19
CZ183195A3 (en)	1996-02-14
HUT75945A (en)	1997-05-28
IL114704A0 (en)	1995-11-27
US5759959A (en)	1998-06-02
TR199500890A2 (tr)	1996-06-21
AU2715195A (en)	1996-03-07
BR9503417A (pt)	1996-06-04
PL309764A1 (en)	1996-02-05
KR960003574A (ko)	1996-02-23
ZA956151B (en)	1997-01-24
CN1119188A (zh)	1996-03-27
TJ95000241A (en)	1998-10-28
NO952940L (no)	1996-01-26

Publication	Publication Date	Title
LV10992B (en)	1996-06-20	4- phenoxycoumarins as herbicidal agents
KR960012178B1 (ko)	1996-09-16	피리미딘 유도체, 그의 제조방법, 제초방법 및 제초조성물
EP0238711B1 (en)	1990-11-28	Thiadiazabicyclononane derivatives, processes for their production and herbizidal compositions
EP0636615A1 (en)	1995-02-01	2-arylaminopyrimidinone derivative, and herbicide and plant growth regulator
EP0532022A1 (en)	1993-03-17	Acrylate compound, preparation process thereof and fungicide using the same
EP0613618A1 (en)	1994-09-07	Method for safening herbicides in crops using substituted benzopyran and tetrahydronaphthalene compounds
RU2066321C1 (ru)	1996-09-10	Производные пиридина или их соли, способ их получения, гербицидная композиция и способ уничтожения сорняков
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