DD301896A9 - Zusammensetzung und Methode zur Verringerung der Phytotoxitaet fuer Kulturpflanzen aufgrund von herbiziden Benzoesaeurederivaten - Google Patents

Zusammensetzung und Methode zur Verringerung der Phytotoxitaet fuer Kulturpflanzen aufgrund von herbiziden Benzoesaeurederivaten Download PDF

Info

Publication number: DD301896A9
Authority: DD; German Democratic Republic
Prior art keywords: alkyl; compound; dichloroacetyl; formula; composition according
Prior art date: 1988-08-01

Application number

DD33124989A

Other languages

German (de)

English (en)

Inventor

Knudt J Miller

Brett H Bussler

Original Assignee

Monsanto 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.)

1988-08-01

Filing date

1989-07-28

Publication date

1994-06-30

1989-07-28 Application filed by Monsanto Co filed Critical Monsanto Co

1994-06-30 Publication of DD301896A9 publication Critical patent/DD301896A9/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 162
230000002363 herbicidal effect Effects 0.000 title claims description 187
238000000034 method Methods 0.000 title claims description 19
231100000674 Phytotoxicity Toxicity 0.000 title claims description 6
244000038559 crop plants Species 0.000 title claims description 6
150000001558 benzoic acid derivatives Chemical class 0.000 title description 7
150000001875 compounds Chemical class 0.000 claims abstract description 140
125000000217 alkyl group Chemical group 0.000 claims abstract description 39
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 31
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 26
150000002367 halogens Chemical class 0.000 claims abstract description 22
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 21
239000001257 hydrogen Substances 0.000 claims abstract description 21
229910052736 halogen Inorganic materials 0.000 claims abstract description 20
150000003839 salts Chemical class 0.000 claims abstract description 17
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 14
125000001424 substituent group Chemical group 0.000 claims abstract description 14
125000003342 alkenyl group Chemical group 0.000 claims abstract description 12
125000000262 haloalkenyl group Chemical group 0.000 claims abstract description 12
125000002541 furyl group Chemical group 0.000 claims abstract description 10
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 7
125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 7
125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 7
125000001544 thienyl group Chemical group 0.000 claims abstract description 6
125000006350 alkyl thio alkyl group Chemical group 0.000 claims abstract description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 4
150000001735 carboxylic acids Chemical class 0.000 claims abstract 3
BLNWTAHYTCHDJH-UHFFFAOYSA-O hydroxy(oxo)azanium Chemical compound O[NH+]=O BLNWTAHYTCHDJH-UHFFFAOYSA-O 0.000 claims abstract 3
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 389
239000000729 antidote Substances 0.000 claims description 216
239000004009 herbicide Substances 0.000 claims description 199
-1 alkoxy radical Chemical class 0.000 claims description 144
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 38
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical group CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims description 34
WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 claims description 31
WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims description 24
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 23
XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims description 21
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 16
150000002431 hydrogen Chemical class 0.000 claims description 14
125000005843 halogen group Chemical group 0.000 claims description 12
125000003545 alkoxy group Chemical group 0.000 claims description 11
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 11
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 10
125000000623 heterocyclic group Chemical group 0.000 claims description 10
125000001841 imino group Chemical group [H]N=* 0.000 claims description 10
SUSQOBVLVYHIEX-UHFFFAOYSA-N phenylacetonitrile Chemical compound N#CCC1=CC=CC=C1 SUSQOBVLVYHIEX-UHFFFAOYSA-N 0.000 claims description 10
229910052757 nitrogen Inorganic materials 0.000 claims description 9
125000004433 nitrogen atom Chemical group N* 0.000 claims description 9
FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims description 8
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 8
150000003254 radicals Chemical class 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 7
229920006395 saturated elastomer Polymers 0.000 claims description 7
YZVFSQQHQPPKNX-UHFFFAOYSA-N 1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C1=CN=CS1 YZVFSQQHQPPKNX-UHFFFAOYSA-N 0.000 claims description 6
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 6
PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
125000000304 alkynyl group Chemical group 0.000 claims description 6
125000001309 chloro group Chemical group Cl* 0.000 claims description 6
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
150000004702 methyl esters Chemical class 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
125000004076 pyridyl group Chemical group 0.000 claims description 6
125000004434 sulfur atom Chemical group 0.000 claims description 6
FJGFHPNQSDXCFC-UHFFFAOYSA-N 1-azaspiro[4.4]nonane Chemical compound C1CCCC21NCCC2 FJGFHPNQSDXCFC-UHFFFAOYSA-N 0.000 claims description 5
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 5
HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 claims description 5
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 claims description 5
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 5
229910052708 sodium Inorganic materials 0.000 claims description 5
239000011734 sodium Substances 0.000 claims description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
GQHLRKZHTIDGFF-UHFFFAOYSA-N 1,5-diazonane Chemical compound C1CCNCCCNC1 GQHLRKZHTIDGFF-UHFFFAOYSA-N 0.000 claims description 4
KWGQOJWITMQEOT-UHFFFAOYSA-N 2-benzhydryloxyacetic acid Chemical compound C=1C=CC=CC=1C(OCC(=O)O)C1=CC=CC=C1 KWGQOJWITMQEOT-UHFFFAOYSA-N 0.000 claims description 4
NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 claims description 4
229960001413 acetanilide Drugs 0.000 claims description 4
125000003277 amino group Chemical group 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
CSVFWMMPUJDVKH-UHFFFAOYSA-N 1,1-dichloropropan-2-one Chemical compound CC(=O)C(Cl)Cl CSVFWMMPUJDVKH-UHFFFAOYSA-N 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 3
125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 3
125000006383 alkylpyridyl group Chemical group 0.000 claims description 3
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical class [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 3
150000003863 ammonium salts Chemical class 0.000 claims description 3
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 3
HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 claims description 3
125000000392 cycloalkenyl group Chemical group 0.000 claims description 3
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
125000000232 haloalkynyl group Chemical group 0.000 claims description 3
125000001041 indolyl group Chemical group 0.000 claims description 3
125000005358 mercaptoalkyl group Chemical group 0.000 claims description 3
STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 claims description 3
125000000160 oxazolidinyl group Chemical group 0.000 claims description 3
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125000004928 piperidonyl group Chemical group 0.000 claims description 3
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XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 3
125000003226 pyrazolyl group Chemical group 0.000 claims description 3
125000000719 pyrrolidinyl group Chemical group 0.000 claims description 3
125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 claims description 3
125000000335 thiazolyl group Chemical group 0.000 claims description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 claims description 2
125000005277 alkyl imino group Chemical group 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims description 2
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BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 claims description 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 8
LPCHEYGJJBDGHB-UHFFFAOYSA-N 2,2-dichloro-1-(2-methyl-3,4-dihydro-2h-quinolin-1-yl)ethanone Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)CCC2=C1 LPCHEYGJJBDGHB-UHFFFAOYSA-N 0.000 claims 4
PFBUKDPBVNJDEW-UHFFFAOYSA-N dichlorocarbene Chemical group Cl[C]Cl PFBUKDPBVNJDEW-UHFFFAOYSA-N 0.000 claims 4
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QQRKRAQOBUDCRQ-UHFFFAOYSA-N ethyl 3-bromo-5-[(4-methoxy-6-methylpyrimidin-2-yl)carbamoylsulfamoyl]-1-methylpyrazole-4-carboxylate Chemical compound BrC1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(C)N=2)=C1C(=O)OCC QQRKRAQOBUDCRQ-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
229960004285 fomepizole Drugs 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
244000304962 green bristle grass Species 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
125000004438 haloalkoxy group Chemical group 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229930002839 ionone Natural products 0.000 description 1
150000002499 ionone derivatives Chemical class 0.000 description 1
150000002545 isoxazoles Chemical class 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
FFPNHFRVPAMADN-UHFFFAOYSA-N methyl 3-chloro-5-[(4-methoxy-6-methylpyrimidin-2-yl)carbamoylsulfamoyl]-1-methylpyrazole-4-carboxylate Chemical compound ClC1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(C)N=2)=C1C(=O)OC FFPNHFRVPAMADN-UHFFFAOYSA-N 0.000 description 1
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
125000006682 monohaloalkyl group Chemical group 0.000 description 1
BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
SFDJOSRHYKHMOK-UHFFFAOYSA-N nitramide Chemical class N[N+]([O-])=O SFDJOSRHYKHMOK-UHFFFAOYSA-N 0.000 description 1
XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 1
LJDZFAPLPVPTBD-UHFFFAOYSA-N nitroformic acid Chemical class OC(=O)[N+]([O-])=O LJDZFAPLPVPTBD-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
LIXFJRLISFERDN-UHFFFAOYSA-N o-ethyl n,n-dipropylcarbamothioate Chemical compound CCCN(CCC)C(=S)OCC LIXFJRLISFERDN-UHFFFAOYSA-N 0.000 description 1
239000005416 organic matter Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
ZVTQYRVARPYRRE-UHFFFAOYSA-N oxadiazol-4-one Chemical class O=C1CON=N1 ZVTQYRVARPYRRE-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
125000002071 phenylalkoxy group Chemical group 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
125000006684 polyhaloalkyl group Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
230000002265 prevention Effects 0.000 description 1
AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
229940080818 propionamide Drugs 0.000 description 1
150000005599 propionic acid derivatives Chemical class 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
GVBSRTBYUFJDIW-UHFFFAOYSA-N pyridine-3,5-dicarbothioic s-acid Chemical compound OC(=S)C1=CN=CC(C(O)=S)=C1 GVBSRTBYUFJDIW-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
DJXNJVFEFSWHLY-UHFFFAOYSA-N quinoline-3-carboxylic acid Chemical compound C1=CC=CC2=CC(C(=O)O)=CN=C21 DJXNJVFEFSWHLY-UHFFFAOYSA-N 0.000 description 1
235000009736 ragweed Nutrition 0.000 description 1
230000004044 response Effects 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000013514 silicone foam Substances 0.000 description 1
238000002791 soaking Methods 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000001593 sorbitan monooleate Substances 0.000 description 1
229940035049 sorbitan monooleate Drugs 0.000 description 1
235000011069 sorbitan monooleate Nutrition 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
238000004544 sputter deposition Methods 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
125000000475 sulfinyl group Chemical class [*:2]S([*:1])=O 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
150000008054 sulfonate salts Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 1
150000003557 thiazoles Chemical class 0.000 description 1
150000003628 tricarboxylic acids 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
230000004222 uncontrolled growth Effects 0.000 description 1
235000020234 walnut Nutrition 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene 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
- 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
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD33124989A 1988-08-01 1989-07-28 Zusammensetzung und Methode zur Verringerung der Phytotoxitaet fuer Kulturpflanzen aufgrund von herbiziden Benzoesaeurederivaten DD301896A9 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US22692888A	1988-08-01	1988-08-01
US36946189A	1989-06-26	1989-06-26

Publications (1)

Publication Number	Publication Date
DD301896A9 true DD301896A9 (de)	1994-06-30

Family

ID=26920996

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD33124989A DD301896A9 (de)	1988-08-01	1989-07-28	Zusammensetzung und Methode zur Verringerung der Phytotoxitaet fuer Kulturpflanzen aufgrund von herbiziden Benzoesaeurederivaten

Country Status (12)

Country	Link
EP (1)	EP0354201A3 (da)
JP (1)	JPH0291004A (da)
KR (1)	KR920001504B1 (da)
CN (1)	CN1039949A (da)
AU (1)	AU624169B2 (da)
BR (1)	BR8903782A (da)
DD (1)	DD301896A9 (da)
DK (1)	DK372889A (da)
HR (1)	HRP920515A2 (da)
IL (1)	IL91142A0 (da)
PT (1)	PT91318A (da)
YU (1)	YU48319B (da)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5201933A (en) *	1988-08-01	1993-04-13	Monsanto Company	Safening herbicidal benzoic acid derivatives
DE4132774A1 (de) *	1991-10-02	1993-04-08	Henkel Kgaa	Stark wirkende antimikrobielle wirkstoffe
EP0546230A1 (en) *	1991-12-10	1993-06-16	Merrell Dow Pharmaceuticals Inc.	Novel process for preparing 4-amino-5-hexenoic acid
UA63884C2 (en) *	1995-04-12	2004-02-16	Singenta Participations Ag	Herbicidal composition and a method of controlling the emergence of undesirable plants
EP0795269B1 (en) *	1996-03-13	2003-07-30	Syngenta Participations AG	Herbicidal combinations
US6586367B2 (en)	1996-09-05	2003-07-01	Syngenta Crop Protection, Inc.	Process for the control of weeds
AU7527898A (en) *	1997-04-23	1998-11-13	Novartis Ag	Herbicide
AU2005236055B2 (en)	2004-04-20	2011-10-06	Transtech Pharma, Llc	Substituted thiazole and pyrimidine derivatives as melanocortin receptor modulators
CN102578084B (zh) *	2004-08-11	2014-06-11	组合化学工业株式会社	农药组合物
US8563742B2 (en)	2008-08-29	2013-10-22	High Point Pharmaceuticals, Llc	Substituted aminothiazole derivatives, pharmaceutical compositions, and methods of use

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH624552A5 (da) *	1975-09-04	1981-08-14	Ciba Geigy Ag
US4269775A (en) *	1978-09-01	1981-05-26	Ciba-Geigy Corporation	Oxime derivatives for protecting plant crops
US4288384A (en) *	1979-09-07	1981-09-08	Stauffer Chemical Company	N-Cyanoalkyl haloacetamides herbicidal antidotes
US5225570A (en) *	1987-08-13	1993-07-06	Monsanto Company	5-heterocyclic-substituted oxazolidine dihaloacetamides

1989
- 1989-07-25 YU YU148989A patent/YU48319B/sh unknown
- 1989-07-28 AU AU39060/89A patent/AU624169B2/en not_active Ceased
- 1989-07-28 EP EP19890870117 patent/EP0354201A3/en not_active Withdrawn
- 1989-07-28 BR BR898903782A patent/BR8903782A/pt not_active IP Right Cessation
- 1989-07-28 DK DK372889A patent/DK372889A/da not_active Application Discontinuation
- 1989-07-28 KR KR1019890010761A patent/KR920001504B1/ko not_active Expired
- 1989-07-28 DD DD33124989A patent/DD301896A9/de unknown
- 1989-07-28 CN CN89105533A patent/CN1039949A/zh active Pending
- 1989-07-28 PT PT91318A patent/PT91318A/pt unknown
- 1989-07-28 IL IL91142A patent/IL91142A0/xx unknown
- 1989-07-28 JP JP1196432A patent/JPH0291004A/ja active Pending
1992
- 1992-09-26 HR HRP920515AA patent/HRP920515A2/hr not_active Application Discontinuation

Also Published As

Publication number	Publication date
CN1039949A (zh)	1990-02-28
PT91318A (pt)	1990-03-08
JPH0291004A (ja)	1990-03-30
KR910000021A (ko)	1991-01-29
HRP920515A2 (hr)	1994-04-30
YU48319B (sh)	1998-05-15
YU148989A (en)	1991-10-31
DK372889A (da)	1990-02-02
EP0354201A3 (en)	1991-10-09
EP0354201A2 (en)	1990-02-07
IL91142A0 (en)	1990-03-19
KR920001504B1 (ko)	1992-02-15
BR8903782A (pt)	1990-03-20
AU3906089A (en)	1990-02-01
AU624169B2 (en)	1992-06-04
DK372889D0 (da)	1989-07-28

Legal Events

Date	Code	Title	Description
1994-06-30	A9	Laid open application accord. to par. 10.3 extension act

Publication	Publication Date	Title
DE69130956T2 (de)	1999-10-07	Verminderung der wechselwirkung zwischen pestizide auf nutzpflanzen
DE3875556T2 (de)	1993-05-06	5-heterocyclisch substituierte oxazolidin-halogenacetamide.
EP0094349B1 (de)	1994-04-06	Verwendung von Chinolinderivaten zum Schützen von Kulturpflanzen
DE3884076T2 (de)	1994-02-10	Herbizide Zusammensetzungen von acylierten 1,3-Dicarbonyl-Herbiziden und Antidots dafür.
DE3817192A1 (de)	1989-11-30	1,2,4-triazolderivate enthaltende pflanzenschuetzende mittel sowie neue derivate des 1,2,4-triazols
DE69607827T2 (de)	2000-10-12	Herbizide zusammensetzungen von 4-benzoylisoxazolen oder 2-cyano-1,3-dionherbiziden und antidots für diese
DD234604A5 (de)	1986-04-09	Verfahren zur selektiven unkrautbekaempfung in nutzpflanzenkulturen
DD208066A5 (de)	1984-03-28	Verfahren zum schuetzen von kulturpflanzen gegen schaedigende wirkungen von aggressiven agrarchemikalien
EP0492367A2 (de)	1992-07-01	Mischungen aus Herbiziden und Antidots
EP0943240B1 (de)	2001-11-14	Kombinationen aus Herbiziden und pflanzenschützenden Stoffen
DE19842894A1 (de)	2000-03-23	Synergistische Wirkstoffkombinationen zur Bekämpfung von Schadpflanzen in Nutzpflanzenkulturen
EP0152006B1 (de)	1989-02-08	Verwendung von Chinolyloxy-Verbindungen als Antidots für Fenoxapropethyl (Ethyl-2[4-(6-chlorbenzoxazolyloxy)-phenoxy]-propionat)
EP0480902A1 (en)	1992-04-15	Safening herbicidal benzoic acid derivatives
EP0149974B1 (de)	1988-09-21	Mittel zum Schützen von Kulturpflanzen vor der phytotoxischen Wirkung von Herbiziden
KR920007609B1 (ko)	1992-09-08	독성이 완화된 이미다졸리논 제초제
DD301896A9 (de)	1994-06-30	Zusammensetzung und Methode zur Verringerung der Phytotoxitaet fuer Kulturpflanzen aufgrund von herbiziden Benzoesaeurederivaten
EP1290946B1 (de)	2004-03-31	Herbizides Mittel
EP0768034A1 (de)	1997-04-16	Herbizides synergistisches Mittel und Verfahren zur Unkrautbekämpfung
DE69227778T2 (de)	1999-07-01	Safener für herbizide pyrazolylsulfonylharnstoffe
DE4236475A1 (de)	1994-06-09	Herbizide Mittel zur Unkrautbekämpfung in Reiskulturen
EP0431545A2 (de)	1991-06-12	Selektive herbizide Mittel und fungizide Mittel
EP0397602A1 (de)	1990-11-14	Neue N-Phenylpyrrolidine
EP0126710B1 (de)	1987-09-30	Mittel zum Schützen von Kulturpflanzen vor der phytotoxischen Wirkung von Herbiziden
EP0480306B1 (de)	1995-08-30	Synergistische herbizide Mittel
DE4241629A1 (de)	1994-06-16	Synergistische herbizide Mittel und Safener