DD262573A5 - Herbizide mittel - Google Patents

Herbizide mittel Download PDF

Info

Publication number: DD262573A5
Authority: DD; German Democratic Republic
Prior art keywords: alkyl; alkoxy; halogen; alkoxycarbonyl; formula
Prior art date: 1986-10-24

Application number

DD87308189A

Other languages

German (de)

English (en)

Inventor

Michael Frey

Heinz Erhardt

Hilmar Mildenberger

Klaus Bauer

Hermann Bieringer

Original Assignee

��@��k��

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.)

1986-10-24

Filing date

1987-10-22

Publication date

1988-12-07

1987-10-22 Application filed by ��@��k�� filed Critical ��@��k��

1988-12-07 Publication of DD262573A5 publication Critical patent/DD262573A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 11
239000004009 herbicide Substances 0.000 title claims abstract description 5
150000001875 compounds Chemical class 0.000 claims abstract description 34
239000004480 active ingredient Substances 0.000 claims abstract description 18
239000000203 mixture Substances 0.000 claims abstract description 16
125000000217 alkyl group Chemical group 0.000 claims abstract description 12
-1 nicotinoyl Chemical group 0.000 claims abstract description 12
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 7
LOTBYPQQWICYBB-UHFFFAOYSA-N methyl n-hexyl-n-[2-(hexylamino)ethyl]carbamate Chemical compound CCCCCCNCCN(C(=O)OC)CCCCCC LOTBYPQQWICYBB-UHFFFAOYSA-N 0.000 claims abstract description 5
125000003342 alkenyl group Chemical group 0.000 claims abstract 2
229910052736 halogen Inorganic materials 0.000 claims description 15
150000002367 halogens Chemical class 0.000 claims description 13
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 10
238000009472 formulation Methods 0.000 claims description 7
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 6
229910052760 oxygen Inorganic materials 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
125000005133 alkynyloxy group Chemical group 0.000 claims description 2
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
125000004076 pyridyl group Chemical group 0.000 claims description 2
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
150000003839 salts Chemical class 0.000 abstract description 9
125000005079 alkoxycarbonylmethyl group Chemical group 0.000 abstract description 2
125000000392 cycloalkenyl group Chemical group 0.000 abstract description 2
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 abstract 6
125000000753 cycloalkyl group Chemical group 0.000 abstract 2
101100477978 Hypocrea jecorina (strain QM6a) sor6 gene Proteins 0.000 abstract 1
125000000304 alkynyl group Chemical group 0.000 abstract 1
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
125000001309 chloro group Chemical group Cl* 0.000 description 55
241000196324 Embryophyta Species 0.000 description 21
230000000694 effects Effects 0.000 description 11
150000003254 radicals Chemical class 0.000 description 11
239000003921 oil Substances 0.000 description 10
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
230000012010 growth Effects 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000000126 substance Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 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 description 5
239000002253 acid Substances 0.000 description 5
239000013543 active substance Substances 0.000 description 5
239000012141 concentrate Substances 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
238000002156 mixing Methods 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
239000011734 sodium Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000000460 chlorine Substances 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
238000000227 grinding Methods 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
239000002689 soil Substances 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
150000003931 anilides Chemical class 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
239000003337 fertilizer Substances 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
239000002585 base Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
244000038559 crop plants Species 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000000284 extract Substances 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000000945 filler Substances 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
239000007787 solid Substances 0.000 description 2
238000009331 sowing Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
230000009105 vegetative growth Effects 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
238000009736 wetting Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
HOQOADCYROWGQA-UHFFFAOYSA-N 1,3-thiazinane Chemical group C1CNCSC1 HOQOADCYROWGQA-UHFFFAOYSA-N 0.000 description 1
WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical compound [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 description 1
YUGUNXGHQJDZJY-UHFFFAOYSA-N 1-diethoxyphosphorylpiperidine Chemical compound CCOP(=O)(OCC)N1CCCCC1 YUGUNXGHQJDZJY-UHFFFAOYSA-N 0.000 description 1
QIINMEGWTDLIJO-UHFFFAOYSA-N 1-ethoxycarbonylpiperidine-2-carboxylic acid Chemical compound CCOC(=O)N1CCCCC1C(O)=O QIINMEGWTDLIJO-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
CMJUNAQINNWKAU-KTKRTIGZSA-N 2-[[(z)-2-oxononadec-10-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)CNCCS(O)(=O)=O CMJUNAQINNWKAU-KTKRTIGZSA-N 0.000 description 1
AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
241000219144 Abutilon Species 0.000 description 1
241000743985 Alopecurus Species 0.000 description 1
241000219318 Amaranthus Species 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
235000006463 Brassica alba Nutrition 0.000 description 1
244000140786 Brassica hirta Species 0.000 description 1
125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
101150065749 Churc1 gene Proteins 0.000 description 1
241000132536 Cirsium Species 0.000 description 1
RHVRIAWHCRJMRY-UHFFFAOYSA-N ClC1=CC=C(NC(=O)C2N(CCCC2)P(=O)(OCC)OCC)C=C1 Chemical compound ClC1=CC=C(NC(=O)C2N(CCCC2)P(=O)(OCC)OCC)C=C1 RHVRIAWHCRJMRY-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
235000004035 Cryptotaenia japonica Nutrition 0.000 description 1
235000017896 Digitaria Nutrition 0.000 description 1
241001303487 Digitaria <clam> Species 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
241000192043 Echinochloa Species 0.000 description 1
244000058871 Echinochloa crus-galli Species 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241001101998 Galium Species 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
240000007171 Imperata cylindrica Species 0.000 description 1
235000021506 Ipomoea Nutrition 0.000 description 1
241000207783 Ipomoea Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000520028 Lamium Species 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
244000100545 Lolium multiflorum Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
102100038239 Protein Churchill Human genes 0.000 description 1
241000219053 Rumex Species 0.000 description 1
241000209056 Secale Species 0.000 description 1
235000007238 Secale cereale Nutrition 0.000 description 1
244000275012 Sesbania cannabina Species 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
240000006394 Sorghum bicolor Species 0.000 description 1
235000011684 Sorghum saccharatum Nutrition 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
102000007641 Trefoil Factors Human genes 0.000 description 1
235000015724 Trifolium pratense Nutrition 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
240000005592 Veronica officinalis Species 0.000 description 1
241001464837 Viridiplantae Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
230000006578 abscission Effects 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
FABHBJUSRZUNRG-NRFANRHFSA-N acropyrone Natural products COc1c(CC=C(C)C)c(O)c([C@H](CC(C)C)c2c(O)c3C=CC(C)(C)Oc3c(C(=O)C)c2O)c(O)c1C(=O)C FABHBJUSRZUNRG-NRFANRHFSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000007900 aqueous suspension 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
239000011230 binding agent Substances 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000000470 constituent Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
LGTLXDJOAJDFLR-UHFFFAOYSA-N diethyl chlorophosphate Chemical compound CCOP(Cl)(=O)OCC LGTLXDJOAJDFLR-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
238000001914 filtration Methods 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000005457 ice water Substances 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
HXEACLLIILLPRG-RXMQYKEDSA-N l-pipecolic acid Natural products OC(=O)[C@H]1CCCCN1 HXEACLLIILLPRG-RXMQYKEDSA-N 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
FRSXFKMXRLYCJW-UHFFFAOYSA-N n-(4-chlorophenyl)piperidine-2-carboxamide Chemical compound C1=CC(Cl)=CC=C1NC(=O)C1NCCCC1 FRSXFKMXRLYCJW-UHFFFAOYSA-N 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-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
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
HXEACLLIILLPRG-UHFFFAOYSA-N pipecolic acid Chemical compound OC(=O)C1CCCCN1 HXEACLLIILLPRG-UHFFFAOYSA-N 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
230000036435 stunted growth Effects 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/04—1,3-Thiazines; Hydrogenated 1,3-thiazines
- C07D279/06—1,3-Thiazines; Hydrogenated 1,3-thiazines not condensed with other rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/10—1,4-Thiazines; Hydrogenated 1,4-thiazines
- C07D279/12—1,4-Thiazines; Hydrogenated 1,4-thiazines not condensed with other rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Hydrogenated Pyridines (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

DD87308189A 1986-10-24 1987-10-22 Herbizide mittel DD262573A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19863636278 DE3636278A1 (de)	1986-10-24	1986-10-24	Herbizide mittel auf der basis von cyclischen (alpha)-iminocarbon-saeureaniliden sowie neue (alpha)-iminocarbonsaeureanilide und verfahren zu ihrer herstellung

Publications (1)

Publication Number	Publication Date
DD262573A5 true DD262573A5 (de)	1988-12-07

Family

ID=6312434

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD87308189A DD262573A5 (de)	1986-10-24	1987-10-22	Herbizide mittel

Country Status (9)

Country	Link
EP (1)	EP0264865A2 (fr)
JP (1)	JPS63115861A (fr)
AU (1)	AU8007587A (fr)
BR (1)	BR8705695A (fr)
DD (1)	DD262573A5 (fr)
DE (1)	DE3636278A1 (fr)
HU (1)	HUT47907A (fr)
IL (1)	IL84233A0 (fr)
ZA (1)	ZA877974B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8823775D0 (en) *	1988-10-11	1988-11-16	Scras	New 2-carbonyl substituted n n'-di-(trimethoxybenzoyl)piperazines
GB9110693D0 (en) *	1991-05-17	1991-07-10	Sandoz Ltd	Improvements in or relating to organic compounds
US7056935B2 (en)	1995-06-07	2006-06-06	Gpi Nil Holdings, Inc.	Rotamase enzyme activity inhibitors
DK0927168T3 (da) *	1996-08-28	2003-03-10	Procter & Gamble	1,3-diheterocykliske metalloproteaseinhibitorer
US6331537B1 (en)	1998-06-03	2001-12-18	Gpi Nil Holdings, Inc.	Carboxylic acids and carboxylic acid isosteres of N-heterocyclic compounds
AU1708099A (en)	1998-06-03	1999-12-20	Amgen, Inc.	N-linked sulfonamides of n-heterocyclic carboxylic acids or carboxylic acid isosteres
IL141063A (en) *	1998-08-07	2005-06-19	Applied Research Systems	Derivatives of pyrrolidine-2-carboxylic acid and piperidine-2-carboxylic acids and pharmaceutical compositions comprising said derivatives for treating infertility
US6417189B1 (en)	1999-11-12	2002-07-09	Gpi Nil Holdings, Inc.	AZA compounds, pharmaceutical compositions and methods of use
US7253169B2 (en)	1999-11-12	2007-08-07	Gliamed, Inc.	Aza compounds, pharmaceutical compositions and methods of use
AU1464101A (en)	1999-12-21	2001-07-03	Gpi Nil Holdings, Inc.	Hydantoin derivative compounds, pharmaceutical compositions, and methods of using same
US7906645B2 (en)	2004-12-24	2011-03-15	Astrazeneca Ab	Heterocyclic compounds as ccr2b antagonists
JP5705748B2 (ja) *	2009-02-18	2015-04-22	ベーリンガーインゲルハイムインターナショナルゲゼルシャフトミットベシュレンクテルハフツング	Ｃｂ２受容体を変調する複素環化合物
WO2011088015A1 (fr)	2010-01-15	2011-07-21	Boehringer Ingelheim International Gmbh	Composés qui modulent le récepteur cb2
EP2803668A1 (fr)	2013-05-17	2014-11-19	Boehringer Ingelheim International Gmbh	Nouveau (cyano-dimethyl-methyl)-isoxazoles et - [1,3,4] thiadiazoles

1986
- 1986-10-24 DE DE19863636278 patent/DE3636278A1/de not_active Withdrawn
1987
- 1987-10-17 EP EP87115217A patent/EP0264865A2/fr not_active Withdrawn
- 1987-10-21 IL IL84233A patent/IL84233A0/xx unknown
- 1987-10-22 DD DD87308189A patent/DD262573A5/de unknown
- 1987-10-23 AU AU80075/87A patent/AU8007587A/en not_active Abandoned
- 1987-10-23 JP JP62266684A patent/JPS63115861A/ja active Pending
- 1987-10-23 ZA ZA877974A patent/ZA877974B/xx unknown
- 1987-10-23 HU HU874753A patent/HUT47907A/hu unknown
- 1987-10-23 BR BR8705695A patent/BR8705695A/pt unknown

Also Published As

Publication number	Publication date
DE3636278A1 (de)	1988-05-05
JPS63115861A (ja)	1988-05-20
EP0264865A2 (fr)	1988-04-27
IL84233A0 (en)	1988-03-31
ZA877974B (en)	1988-04-26
HUT47907A (en)	1989-04-28
BR8705695A (pt)	1988-05-31
AU8007587A (en)	1988-04-28

Publication	Publication Date	Title
EP0044809B1 (fr)	1983-08-31	N-(2-substitué phénylsulfonyl)-N'-triazinyl urées
DE69028461T2 (de)	1997-02-06	Triazin-derivate und unkrautvertilgungsmittel daraus
EP0342569B1 (fr)	1994-06-22	2-Alkoxyphénoxysulfonylurées hétérocycliques et leur utilisation comme herbicides ou comme régulateurs de croissance des plantes
CH649081A5 (de)	1985-04-30	Triaza-verbindungen.
DD262573A5 (de)	1988-12-07	Herbizide mittel
EP0336354B1 (fr)	1994-11-02	Composés alkyl- et alcénylsulfonylurées hétérocycliquement substitués, procédés pour leur préparation et leur application comme herbicides ou régulateurs de croissance de végétaux
DD283918A5 (de)	1990-10-31	Herbizide und pflanzenwachsumsregulierende mittel und verfahren zur herstellung der wirkstoffe
DD261084A5 (de)	1988-10-19	1,2-disubstituierte piperidine, verfahren zu ihrer herstellung sowie ihre verwendung im pflanzenschutz
DD249623A5 (de)	1987-09-16	Herbizide mittel
EP0342568B1 (fr)	1994-02-02	Phénoxysulfonylurées substituées par un hétérocycle, procédé pour leur préparation et leur utilisation comme herbicides ou comme régulateurs de croissance des plantes
EP0058639B1 (fr)	1985-08-14	Esters de l'acide 2-(4-(6-halogène-quinoxalinyl-2-oxy)-phénoxy)-propionique, leurs procédés de préparation et leur application comme herbicides et régulateurs de la croissance de plantes
EP0151744B1 (fr)	1989-04-26	1-Acylimidazolinones, procédé de leur préparation et leur application dans l'agriculture
EP0288960A1 (fr)	1988-11-02	Alkyl N-aryltétrahydrophtalimides, procédé pour leur préparation et leur utilisation dans la protection des plantes
EP0145664A2 (fr)	1985-06-19	Sulfonylurées herbicides
EP0303114B1 (fr)	1994-08-24	Phénylesters d'acide sulfamique hétérocycliquement substitués, procédé pour leur préparation et leur utilisation comme herbicides et régulateurs de croissance des plantes
EP0493321A1 (fr)	1992-07-01	Pyrimidinyl- et triazinyl-salicylamides, leur usage et leur préparation
DD300431A5 (de)	1992-06-11	Heterocyclisch substituierte sulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren
DD228160A5 (de)	1985-10-09	Herbizide und wachstumsregulierende mittel
DE3502629A1 (de)	1986-07-31	Phenoxybenzoesaeurederivate, verfahren zu ihrer herstellung sowie ihre verwendung im pflanzenschutz
DD219362A5 (de)	1985-03-06	Herbizides mittel
DE3807532A1 (de)	1989-09-21	Pyrimidin-carbonsaeuren, verfahren zur herstellung und ihre verwendung als herbizide
DE3909053A1 (de)	1990-09-20	Phenoxysulfonylharnstoffe auf basis von 3-substituierten salicylsaeurealkylestern, verfahren zu ihrer herstellung und ihre verwendung als herbizide und pflanzenwachstumsregulatoren
DE3234451A1 (de)	1984-03-22	Neue pyridylharnstoffe, verfahren zu ihrer herstellung, sie enthaltende mittel und deren verwendung als herbizide
DE3234448A1 (de)	1984-03-22	Neue pyrimidinylharnstoffe, verfahren zu ihrer herstellung, sie enthaltende mittel und deren verwendung als herbizide
EP0221439A1 (fr)	1987-05-13	Compositions herbicides contenant des hétérocycles comportant des atomes d'azote et des radicaux arylcarbamyle et dérivés hétérocycliques comportant des radicaux arylcarbamyle