DD231725A5 - Herbizide mittel - Google Patents

Herbizide mittel Download PDF

Info

Publication number: DD231725A5
Authority: DD; German Democratic Republic
Prior art keywords: group; general formula; denotes; nit; och
Prior art date: 1984-01-10

Application number

DD85272457A

Other languages

German (de)

English (en)

Inventor

Kozo Shiokawa

Koichi Moriya

Toshio Goto

Atsumi Kamochi

Shigeo Kohama

Original Assignee

��@��@��@��@�K@�Kk��

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.)

1984-01-10

Filing date

1985-01-08

Publication date

1986-01-08

1985-01-08 Application filed by ��@��@��@��@�K@�Kk�� filed Critical ��@��@��@��@�K@�Kk��

1986-01-08 Publication of DD231725A5 publication Critical patent/DD231725A5/de

Links

239000004009 herbicide Substances 0.000 title claims abstract description 15
230000002363 herbicidal effect Effects 0.000 title claims description 18
125000003545 alkoxy group Chemical group 0.000 claims abstract description 15
VITPICOSHHCBFU-UHFFFAOYSA-N 1-sulfonylguanidine Chemical class NC(=N)N=S(=O)=O VITPICOSHHCBFU-UHFFFAOYSA-N 0.000 claims abstract description 14
125000000217 alkyl group Chemical group 0.000 claims abstract description 12
125000003282 alkyl amino group Chemical group 0.000 claims abstract description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims abstract description 4
-1 2-Ethoxysulfonylbenzolsulfonyl Chemical group 0.000 claims description 28
239000000203 mixture Substances 0.000 claims description 12
239000004606 Fillers/Extenders Substances 0.000 claims description 6
239000004094 surface-active agent Substances 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 5
230000008636 plant growth process Effects 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 abstract description 7
239000004480 active ingredient Substances 0.000 abstract description 6
101100242909 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) pbpA gene Proteins 0.000 abstract 1
101100269618 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) aliA gene Proteins 0.000 abstract 1
101100439974 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) clpE gene Proteins 0.000 abstract 1
101150109310 msrAB1 gene Proteins 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 56
238000000034 method Methods 0.000 description 43
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JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 20
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UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 10
239000002904 solvent Substances 0.000 description 10
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QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
229920001807 Urea-formaldehyde Polymers 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000002280 amphoteric surfactant Substances 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
239000003443 antiviral agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000005667 attractant 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
YBGQXNZTVFEKEN-UHFFFAOYSA-N benzene-1,2-disulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1S(Cl)(=O)=O YBGQXNZTVFEKEN-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
235000011116 calcium hydroxide Nutrition 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
238000005266 casting Methods 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
125000000113 cyclohexyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
125000004119 disulfanediyl group Chemical group *SS* 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
JFEUZPXAGPSPNP-UHFFFAOYSA-N ethyl 2-(methoxysulfamoyl)benzenesulfonate Chemical compound CCOS(=O)(=O)C1=CC=CC=C1S(=O)(=O)NOC JFEUZPXAGPSPNP-UHFFFAOYSA-N 0.000 description 1
HJJVBRKTPUAHPG-UHFFFAOYSA-N ethyl 2-[[(e)-n'-(4,6-dimethylpyrimidin-2-yl)carbamimidoyl]-methoxysulfamoyl]benzenesulfonate Chemical compound CCOS(=O)(=O)C1=CC=CC=C1S(=O)(=O)N(OC)C(N)=NC1=NC(C)=CC(C)=N1 HJJVBRKTPUAHPG-UHFFFAOYSA-N 0.000 description 1
MGTWUROPHXABEF-UHFFFAOYSA-N ethyl 2-chlorosulfonylbenzenesulfonate Chemical compound CCOS(=O)(=O)C1=CC=CC=C1S(Cl)(=O)=O MGTWUROPHXABEF-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000295 fuel oil Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000008103 glucose Substances 0.000 description 1
235000001727 glucose Nutrition 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
230000012010 growth Effects 0.000 description 1
229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
CYPPCCJJKNISFK-UHFFFAOYSA-J kaolinite Chemical compound [OH-].[OH-].[OH-].[OH-].[Al+3].[Al+3].[O-][Si](=O)O[Si]([O-])=O CYPPCCJJKNISFK-UHFFFAOYSA-J 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
210000001699 lower leg Anatomy 0.000 description 1
239000011419 magnesium lime Substances 0.000 description 1
UVJTVPWNRSZXEF-UHFFFAOYSA-N methyl 2-[(e)-[[(4,6-dimethylpyrimidin-2-yl)amino]-(methoxyamino)methylidene]amino]sulfonylbenzenesulfonate Chemical compound C=1C=CC=C(S(=O)(=O)OC)C=1S(=O)(=O)N=C(NOC)NC1=NC(C)=CC(C)=N1 UVJTVPWNRSZXEF-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
CVYUTQOJFVLGNW-UHFFFAOYSA-N methyl n-(4,6-dimethylpyrimidin-2-yl)-n'-(2-morpholin-4-ylsulfonylphenyl)sulfonylcarbamimidothioate Chemical compound C=1C=CC=C(S(=O)(=O)N2CCOCC2)C=1S(=O)(=O)N=C(SC)NC1=NC(C)=CC(C)=N1 CVYUTQOJFVLGNW-UHFFFAOYSA-N 0.000 description 1
BCROWDSKPORTTJ-UHFFFAOYSA-N methyl n-(4,6-dimethylpyrimidin-2-yl)-n'-(2-sulfamoylphenyl)sulfonylcarbamimidothioate Chemical compound C=1C=CC=C(S(N)(=O)=O)C=1S(=O)(=O)N=C(SC)NC1=NC(C)=CC(C)=N1 BCROWDSKPORTTJ-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
238000002156 mixing Methods 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
AQFWNELGMODZGC-UHFFFAOYSA-N o-ethylhydroxylamine Chemical compound CCON AQFWNELGMODZGC-UHFFFAOYSA-N 0.000 description 1
150000004045 organic chlorine compounds Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000002898 organic sulfur compounds Chemical class 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000019809 paraffin wax Nutrition 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
239000010451 perlite Substances 0.000 description 1
235000019362 perlite Nutrition 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000000047 product Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000008262 pumice Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003892 spreading Methods 0.000 description 1
238000004544 sputter deposition Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
244000045561 useful plants Species 0.000 description 1
235000013311 vegetables Nutrition 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
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000010457 zeolite Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
- 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
- A01N47/40—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
- A01N47/44—Guanidine; Derivatives thereof

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DD85272457A 1984-01-10 1985-01-08 Herbizide mittel DD231725A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP59001257A JPS60146878A (ja)	1984-01-10	1984-01-10	スルホニルグアニジン誘導体，その製法及び除草剤

Publications (1)

Publication Number	Publication Date
DD231725A5 true DD231725A5 (de)	1986-01-08

Family

ID=11496401

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85272457A DD231725A5 (de)	1984-01-10	1985-01-08	Herbizide mittel

Country Status (12)

Country	Link
US (1)	US4619688A (pt)
EP (1)	EP0148498A1 (pt)
JP (1)	JPS60146878A (pt)
KR (1)	KR850005418A (pt)
AU (1)	AU3736585A (pt)
BR (1)	BR8500090A (pt)
DD (1)	DD231725A5 (pt)
DK (1)	DK10685A (pt)
ES (1)	ES8607951A1 (pt)
HU (1)	HUT36343A (pt)
IL (1)	IL74010A0 (pt)
ZA (1)	ZA85201B (pt)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3431913A1 (de) *	1984-08-30	1986-03-13	Bayer Ag, 5090 Leverkusen	Oxyguanidin-derivate
DE3431916A1 (de) *	1984-08-30	1986-03-13	Bayer Ag, 5090 Leverkusen	Fluoralkoxyphenylsulfonylguanidine
DE3431918A1 (de) *	1984-08-30	1986-03-13	Bayer Ag, 5090 Leverkusen	Substituierte arylsulfonylguanidine
SE9301595L (sv) *	1993-05-10	1994-10-17	Tony Pervan	Fog för tunna flytande hårda golv
US20030084514A1 (en) *	2001-07-31	2003-05-08	Chan Marie S.	Method of dewrinkling fabrics

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4310346A (en) *	1980-03-14	1982-01-12	E. I. Du Pont De Nemours And Company	N(Substituted phenylsulfonyl) N'(substituted cyumidin-2-yl) ureas
DK259280A (da) *	1979-07-20	1981-01-21	Du Pont	Herbicide sulfonamider
US4404017A (en) *	1980-07-03	1983-09-13	Gulf Oil Corporation	Phthalimidoguanidine plant growth regulators
US4484939A (en) *	1983-02-18	1984-11-27	E. I. Du Pont De Nemours And Company	Herbicidal sulfonamide inner salts

1984
- 1984-01-10 JP JP59001257A patent/JPS60146878A/ja active Pending
- 1984-12-27 EP EP84116306A patent/EP0148498A1/de not_active Withdrawn
1985
- 1985-01-04 US US06/688,844 patent/US4619688A/en not_active Expired - Fee Related
- 1985-01-07 AU AU37365/85A patent/AU3736585A/en not_active Abandoned
- 1985-01-07 IL IL74010A patent/IL74010A0/xx unknown
- 1985-01-08 DD DD85272457A patent/DD231725A5/de unknown
- 1985-01-09 DK DK10685A patent/DK10685A/da unknown
- 1985-01-09 BR BR8500090A patent/BR8500090A/pt unknown
- 1985-01-09 KR KR1019850000075A patent/KR850005418A/ko not_active Application Discontinuation
- 1985-01-09 HU HU8567A patent/HUT36343A/hu unknown
- 1985-01-09 ES ES539429A patent/ES8607951A1/es not_active Expired
- 1985-01-19 ZA ZA85201A patent/ZA85201B/xx unknown

Also Published As

Publication number	Publication date
DK10685A (da)	1985-07-11
US4619688A (en)	1986-10-28
EP0148498A1 (de)	1985-07-17
ES8607951A1 (es)	1986-06-01
ES539429A0 (es)	1986-06-01
JPS60146878A (ja)	1985-08-02
ZA85201B (en)	1986-05-28
BR8500090A (pt)	1985-08-13
DK10685D0 (da)	1985-01-09
HUT36343A (en)	1985-09-30
IL74010A0 (en)	1985-04-30
KR850005418A (ko)	1985-08-26
AU3736585A (en)	1985-07-18

Publication	Publication Date	Title
EP0131258B1 (de)	1989-08-30	Neue N-Alkoxy- N-Alkylsulfonylaminosulfonylharnstoffe, und neue (Pyrimido) Triazino-thiatriazinoxide als Vorprodukte
EP0342569B1 (de)	1994-06-22	Heterocyclische 2-Alkoxyphenoxysulfonylharnstoffe und ihre Verwendung als Herbizide oder Pflanzenwachstumsregulatoren
EP0096003B2 (de)	1994-06-15	Neue Sulfonyl(thio)harnstoffe, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und/oder Wachstumsregulatoren
EP0071958B1 (de)	1985-04-10	Heterocyclisch substituierte Sulfonylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung in der Landwirtschaft
DE2809035A1 (de)	1978-09-07	N'- eckige klammer auf 4-(phenethyloxy)-phenyl eckige klammer zu -n-methyl- n-methoxyharnstoffe, verfahren zu ihrer herstellung und ihre verwendung zur unkrautbekaempfung
DE69126836T2 (de)	1998-01-02	Herbizide
EP0103537B1 (de)	1987-07-08	N-Arylsulfonyl-N'-triazolylharnstoffe
EP0459949A1 (de)	1991-12-04	Sulfonylharnstoffe mit herbizider und pflanzenwuchsregulierender Wirkung
DD231716A5 (de)	1986-01-08	Herbizide mittel
EP0129764A2 (de)	1985-01-02	Substituierte Phenylsulfonylguanidin-Derivate
EP0096004B1 (de)	1989-04-26	Neue Sulfonyl(thio)harnstoffe, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und/oder Wachstumsregulatoren
EP0122231B1 (de)	1990-01-17	Herbizides Mittel
EP0153601B1 (de)	1987-04-01	2-Alkoxyaminosulfonylbenzolsulfonyl-harnstoff-Derivate
DD231725A5 (de)	1986-01-08	Herbizide mittel
DE1914014A1 (de)	1969-10-02	Neue 2-Alkylthio-4,6-diamino-S-triazine
EP0141319B1 (de)	1988-05-25	Substituierte Phenoxyalkancarbonsäureester
EP0342568A1 (de)	1989-11-23	Heterocyclisch substituierte Phenoxysulfonylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide oder Pflanzenwachstumsregulatoren
DE3101889A1 (de)	1982-08-26	"neue phenoxycarbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide"
EP0062254A1 (de)	1982-10-13	Substituierte Acetanilide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide
EP0493321A1 (de)	1992-07-01	Pyrimidinyl- und Triazinyl-salicylamide sowie deren Verwendung und Herstellung
EP0057367B1 (de)	1983-12-28	2-Pyridyloxyacetanilid-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung
EP0092112A1 (de)	1983-10-26	Substituierte Phenoxypropionate
DD275805A5 (de)	1990-02-07	Herbizide und pflanzenwachstumsregulatoren
DE2200290C3 (de)	1980-04-30	N-(1-Alken -l-yl)-amino-s-triazine
DE3234448A1 (de)	1984-03-22	Neue pyrimidinylharnstoffe, verfahren zu ihrer herstellung, sie enthaltende mittel und deren verwendung als herbizide