DD209377A5 - Verfahren zur bekaempfung unerwuenschter vegetation - Google Patents

Verfahren zur bekaempfung unerwuenschter vegetation Download PDF

Info

Publication number: DD209377A5
Authority: DD; German Democratic Republic
Prior art keywords: hydrogen; chloro; item; group; chlorine
Prior art date: 1982-03-25

Application number

DD83249135A

Other languages

German (de)

English (en)

Inventor

William J Michaely

Gary W Kraatz

Original Assignee

Stauffer Chemical 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.)

1982-03-25

Filing date

1983-03-24

Publication date

1984-05-09

1983-03-24 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1984-05-09 Publication of DD209377A5 publication Critical patent/DD209377A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 31
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 34
150000001875 compounds Chemical class 0.000 claims abstract description 33
239000001257 hydrogen Substances 0.000 claims abstract description 33
150000002431 hydrogen Chemical class 0.000 claims abstract description 21
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 11
239000000460 chlorine Substances 0.000 claims abstract description 11
229910052801 chlorine Inorganic materials 0.000 claims abstract description 11
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 10
125000000217 alkyl group Chemical group 0.000 claims abstract description 7
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 7
229910052794 bromium Inorganic materials 0.000 claims abstract description 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 6
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 4
150000002367 halogens Chemical class 0.000 claims abstract description 4
229910052740 iodine Inorganic materials 0.000 claims abstract description 4
239000011630 iodine Substances 0.000 claims abstract description 4
229910052736 halogen Inorganic materials 0.000 claims abstract description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 31
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 5
125000003545 alkoxy group Chemical group 0.000 claims description 2
CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 claims 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 1
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
239000001301 oxygen Substances 0.000 claims 1
229910052760 oxygen Inorganic materials 0.000 claims 1
230000002363 herbicidal effect Effects 0.000 abstract description 22
-1 2- (2-substituted benzoyl) -1,3-cyclohexanediones Chemical class 0.000 abstract description 6
239000000203 mixture Substances 0.000 description 28
239000004009 herbicide Substances 0.000 description 21
241000196324 Embryophyta Species 0.000 description 15
239000004480 active ingredient Substances 0.000 description 13
239000002689 soil Substances 0.000 description 13
239000007788 liquid Substances 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
238000009472 formulation Methods 0.000 description 6
231100000208 phytotoxic Toxicity 0.000 description 6
230000000885 phytotoxic effect Effects 0.000 description 6
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
239000012876 carrier material Substances 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
239000007921 spray Substances 0.000 description 5
240000006995 Abutilon theophrasti Species 0.000 description 4
230000006378 damage Effects 0.000 description 4
239000000428 dust Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
235000003403 Limnocharis flava Nutrition 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000002245 particle Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
235000005074 zinc chloride Nutrition 0.000 description 3
239000011592 zinc chloride Substances 0.000 description 3
244000285774 Cyperus esculentus Species 0.000 description 2
235000005853 Cyperus esculentus Nutrition 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
150000001448 anilines Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
GJQBHOAJJGIPRH-UHFFFAOYSA-N benzoyl cyanide Chemical class N#CC(=O)C1=CC=CC=C1 GJQBHOAJJGIPRH-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000012043 crude product Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
230000002262 irrigation Effects 0.000 description 2
238000003973 irrigation Methods 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000004576 sand Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
SMYMJHWAQXWPDB-UHFFFAOYSA-N (2,4,5-trichlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SMYMJHWAQXWPDB-UHFFFAOYSA-N 0.000 description 1
125000000027 (C1-C10) alkoxy group Chemical group 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
239000003559 2,4,5-trichlorophenoxyacetic acid Substances 0.000 description 1
MJJCNUBDKYFMHM-UHFFFAOYSA-N 2,4-dichlorobenzoyl cyanide Chemical compound ClC1=CC=C(C(=O)C#N)C(Cl)=C1 MJJCNUBDKYFMHM-UHFFFAOYSA-N 0.000 description 1
OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
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 1
FBMDQVBGIYSDTI-UHFFFAOYSA-N 2-n,4-n-bis(3-methoxypropyl)-6-methylsulfanyl-1,3,5-triazine-2,4-diamine Chemical compound COCCCNC1=NC(NCCCOC)=NC(SC)=N1 FBMDQVBGIYSDTI-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
NAOCHJCREOAPOF-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-1,1-dimethylurea Chemical compound CN(C)C(=O)NC1=CC(Cl)=CC(Cl)=C1 NAOCHJCREOAPOF-UHFFFAOYSA-N 0.000 description 1
125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
244000178993 Brassica juncea Species 0.000 description 1
235000011332 Brassica juncea Nutrition 0.000 description 1
235000014700 Brassica juncea var napiformis Nutrition 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-N 0.000 description 1
HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
241000032989 Ipomoea lacunosa Species 0.000 description 1
239000005574 MCPA Substances 0.000 description 1
244000088461 Panicum crus-galli Species 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
240000001398 Typha domingensis Species 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
150000003869 acetamides Chemical class 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000000304 alkynyl group Chemical group 0.000 description 1
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000006286 aqueous extract Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
150000001559 benzoic acids Chemical class 0.000 description 1
238000009835 boiling Methods 0.000 description 1
YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
239000011362 coarse particle Substances 0.000 description 1
239000002361 compost Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
150000001879 copper Chemical class 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
HJSLFCCWAKVHIW-UHFFFAOYSA-N cyclohexane-1,3-dione Chemical compound O=C1CCCC(=O)C1 HJSLFCCWAKVHIW-UHFFFAOYSA-N 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
150000004659 dithiocarbamates Chemical class 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000284 extract Substances 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000003864 humus Substances 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
229910003480 inorganic solid Inorganic materials 0.000 description 1
239000003621 irrigation water Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000003350 kerosene 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
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
238000002156 mixing Methods 0.000 description 1
DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 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
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
239000010451 perlite Substances 0.000 description 1
235000019362 perlite Nutrition 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000000630 rising effect Effects 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
241000894007 species Species 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000003419 tautomerization reaction Methods 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
231100000167 toxic agent Toxicity 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
238000009834 vaporization Methods 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/45—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by at least one doubly—bound oxygen atom, not being part of a —CHO group
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/80—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen
- C07C49/813—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen polycyclic

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Environmental Sciences (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catching Or Destruction (AREA)

DD83249135A 1982-03-25 1983-03-24 Verfahren zur bekaempfung unerwuenschter vegetation DD209377A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US36165882A	1982-03-25	1982-03-25
US46425183A	1983-02-09	1983-02-09

Publications (1)

Publication Number	Publication Date
DD209377A5 true DD209377A5 (de)	1984-05-09

Family

ID=27001374

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD83249135A DD209377A5 (de)	1982-03-25	1983-03-24	Verfahren zur bekaempfung unerwuenschter vegetation

Country Status (21)

Country	Link
EP (1)	EP0090262B1 (ro)
KR (1)	KR890002635B1 (ro)
AU (1)	AU560068B2 (ro)
BG (1)	BG38931A3 (ro)
BR (1)	BR8301522A (ro)
CA (1)	CA1217204A (ro)
CS (1)	CS236789B2 (ro)
DD (1)	DD209377A5 (ro)
DE (1)	DE3382601T2 (ro)
DK (1)	DK156135C (ro)
ES (1)	ES8500881A1 (ro)
GR (1)	GR77167B (ro)
IE (1)	IE59474B1 (ro)
IL (1)	IL68231A (ro)
NO (1)	NO156607C (ro)
NZ (1)	NZ203678A (ro)
PH (1)	PH17866A (ro)
PL (1)	PL144046B1 (ro)
PT (1)	PT76418B (ro)
RO (1)	RO89692A (ro)
YU (1)	YU43159B (ro)

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US4767447A (en) *	1986-09-12	1988-08-30	Stauffer Chemical Company	Certain 2-(substituted benzoyl)-5-(substituted or unsubstituted phenyl)-1,3-cyclohexanediones
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US4938796A (en) *	1987-07-06	1990-07-03	Ici Americas Inc.	Herbicidal compositions of acylated 1,3-dicarbonyl herbicides and antidotes therefor
US4859234A (en) *	1987-09-14	1989-08-22	Ici Americas Inc.	Herbicidal compositions of acylated 1,3-dicarbonyl herbicides and phenoxyalkanoic acids, salts, amides and esters therof as antidotes
IL91083A (en) *	1988-07-25	1993-04-04	Ciba Geigy	Cyclohexanedione derivatives, their preparation and their use as herbicides
US4957538A (en) *	1988-11-18	1990-09-18	Ici Americas Inc.	Certain 2-(2',3',4'-trisubstituted benzoyl)-1,3-cyclohexanediones
US5336662A (en) *	1989-04-25	1994-08-09	Sandoz Ltd.	Heterocyclic diones as plant growth regulators
KR927002913A (ko) *	1989-10-18	1992-12-17	짜우너, 라피체	제초 활성 물질 혼합물
KR927003554A (ko) *	1990-10-25	1992-12-18	예안 크레이머	살충제 및 식물 생장 조절제로서의 헤테로 사이클계 디온 유도체
MX9200956A (es) *	1991-03-06	1993-09-01	Hoechst Ag	Benzoilciclohexanodionas substituidas con haloalcoxi en calidad de herbicidad y reguladoras del crecimiento de las plantas
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CN1597672A (zh)	1998-07-24	2005-03-23	拜尔公司	取代的苯甲酰基环己二酮类化合物
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1983
- 1983-03-16 EP EP83102599A patent/EP0090262B1/en not_active Expired
- 1983-03-16 DE DE8383102599T patent/DE3382601T2/de not_active Expired - Fee Related
- 1983-03-18 YU YU659/83A patent/YU43159B/xx unknown
- 1983-03-21 PT PT76418A patent/PT76418B/pt unknown
- 1983-03-22 PH PH28673A patent/PH17866A/en unknown
- 1983-03-22 GR GR70838A patent/GR77167B/el unknown
- 1983-03-23 CS CS831984A patent/CS236789B2/cs unknown
- 1983-03-23 DK DK131783A patent/DK156135C/da not_active IP Right Cessation
- 1983-03-24 RO RO83110450A patent/RO89692A/ro unknown
- 1983-03-24 NO NO831058A patent/NO156607C/no unknown
- 1983-03-24 CA CA000424381A patent/CA1217204A/en not_active Expired
- 1983-03-24 AU AU12768/83A patent/AU560068B2/en not_active Ceased
- 1983-03-24 IL IL68231A patent/IL68231A/xx not_active IP Right Cessation
- 1983-03-24 ES ES520957A patent/ES8500881A1/es not_active Expired
- 1983-03-24 KR KR1019830001192A patent/KR890002635B1/ko not_active Expired
- 1983-03-24 BR BR8301522A patent/BR8301522A/pt unknown
- 1983-03-24 NZ NZ203678A patent/NZ203678A/en unknown
- 1983-03-24 IE IE64983A patent/IE59474B1/en not_active IP Right Cessation
- 1983-03-24 DD DD83249135A patent/DD209377A5/de unknown
- 1983-03-24 PL PL1983241172A patent/PL144046B1/pl unknown
- 1983-03-25 BG BG060289A patent/BG38931A3/xx unknown

Also Published As

Publication number	Publication date
DK131783D0 (da)	1983-03-23
IL68231A0 (en)	1983-06-15
ES520957A0 (es)	1984-11-01
AU560068B2 (en)	1987-03-26
CS236789B2 (en)	1985-05-15
BR8301522A (pt)	1983-12-06
NO831058L (no)	1983-09-26
PH17866A (en)	1985-01-14
DE3382601D1 (en)	1992-09-10
BG38931A3 (en)	1986-03-14
PL241172A1 (en)	1984-01-02
YU43159B (en)	1989-04-30
DK131783A (da)	1983-09-26
IL68231A (en)	1986-08-31
KR840003776A (ko)	1984-10-04
PT76418A (en)	1983-04-01
GR77167B (ro)	1984-09-10
NZ203678A (en)	1987-01-23
NO156607C (no)	1987-10-21
ES8500881A1 (es)	1984-11-01
EP0090262B1 (en)	1992-08-05
IE59474B1 (en)	1994-03-09
NO156607B (no)	1987-07-13
YU65983A (en)	1986-02-28
IE830649L (en)	1983-09-25
DK156135B (da)	1989-06-26
EP0090262A2 (en)	1983-10-05
PT76418B (en)	1986-11-13
EP0090262A3 (en)	1984-03-28
DE3382601T2 (de)	1993-01-07
CA1217204A (en)	1987-01-27
DK156135C (da)	1989-11-06
RO89692A (ro)	1986-06-30
PL144046B1 (en)	1988-04-30
AU1276883A (en)	1983-09-29
KR890002635B1 (ko)	1989-07-21

Publication	Publication Date	Title
DE3382601T2 (de)	1993-01-07	2-(2-substituierte benzoyl)-1,3 cyclohexandione.
DD233150A5 (de)	1986-02-19	Herbizide mittel
DD247210A5 (de)	1987-07-01	Verfahren zur herstellung von 2'-(2'-nitrobenzol)-1,-3-cyclohexandienen
DE1643527B2 (de)	1979-02-22	N,N-Disubstituierte Alanine und deren Verwendung als Herbicide
DD232416A5 (de)	1986-01-29	Herbizide mittel
DE2822304A1 (de)	1978-11-30	Substituierte cyclohexan-1,3-dion- derivate
DD247211A5 (de)	1987-07-01	Verfahren zur herstellung von 2-(2'-alkylbenzol)-1,3-cyclohexandienen
DE2417487A1 (de)	1975-10-30	Herbizide mittel
EP0003805B1 (de)	1982-06-30	Pyridazonverbindungen und diese enthaltende herbizide Zusammensetzungen
DE2744169A1 (de)	1978-04-06	N-eckige klammer auf 4-(subst.- benzyloxy)-phenyl eckige klammer zu -n'- methyl-n'-methoxyharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide
EP0036390B1 (de)	1983-10-26	Diphenyläther-Harnstoffe mit herbizider Wirkung
DE1542943A1 (de)	1972-04-06	Herbizide
CH644096A5 (de)	1984-07-13	N-benzylhalogenacetamidderivate.
EP0007089B1 (de)	1981-09-16	Acylanilide mit herbicider und fungicider Wirkung, Verfahren zu ihrer Herstellung und ihre Verwendung
CH646941A5 (de)	1984-12-28	N-dimethylbenzylacetamidderivate.
EP0018585B1 (de)	1984-02-08	Parabansäurederivate, Herbizide, die diese Verbindungen enthalten, und Verfahren zur Herstellung der Herbizide
EP0095099B1 (de)	1986-08-20	Cyclohexan-1,3-dion-Derivate
DD262992A5 (de)	1988-12-21	Nematizide und insektizide zusammensetzung
DE2918541A1 (de)	1979-11-15	Diphenylaminderivate und verfahren zu deren herstellung
EP0072348A2 (de)	1983-02-16	Neue Phenoxyphenyl-aminosäure-Derivate, ihre Herstellung, sie enthaltende Mittel sowie ihre Verwendung
EP0067381B1 (de)	1984-03-21	Anilide, Verfahren zu ihrer Herstellung und diese enthaltende Herbizide
DE1914015C3 (de)	1978-08-24	a-ChloM-tertbutylamino-e-cyclopropylamino-s-triazin und dieses enthaltende Mittel zur Bekämpfung von Unkräutern
DE2021822A1 (de)	1970-11-19	Acylierte Triflourmethylharnstoffcarbamate und deren Verwendung als Herbizide
EP0114299A2 (de)	1984-08-01	Phenylglyoxylsäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
EP0174680B1 (en)	1988-07-06	Substituted 4-fluorothiocarbanilide herbicidal compounds and methods of use