CH501358A - Herbicides Mittel - Google Patents

Herbicides Mittel

Info

Publication number: CH501358A
Authority: CH; Switzerland
Prior art keywords: sep; group; hydrogen atom; methyl; active ingredient
Prior art date: 1966-06-08

Application number

CH795867A

Other languages

German (de)

English (en)

Inventor

Yates John

John Devlin Barry Roy

Original Assignee

Shell Int Research

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.)

1966-06-08

Filing date

1967-06-06

Publication date

1971-01-15

1967-06-06 Application filed by Shell Int Research filed Critical Shell Int Research

1971-01-15 Publication of CH501358A publication Critical patent/CH501358A/de

Links

239000004009 herbicide Substances 0.000 title claims abstract description 23
238000002360 preparation method Methods 0.000 title claims description 17
-1 amino, carbamoyl Chemical group 0.000 claims abstract description 76
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 37
125000000217 alkyl group Chemical group 0.000 claims abstract description 22
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 21
125000003342 alkenyl group Chemical group 0.000 claims abstract description 14
125000002947 alkylene group Chemical group 0.000 claims abstract description 12
125000003118 aryl group Chemical group 0.000 claims abstract description 10
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 6
125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 claims abstract description 4
125000005842 heteroatom Chemical group 0.000 claims abstract description 4
150000001875 compounds Chemical class 0.000 claims description 39
241000196324 Embryophyta Species 0.000 claims description 28
239000004480 active ingredient Substances 0.000 claims description 25
229910052801 chlorine Inorganic materials 0.000 claims description 24
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 21
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
238000005507 spraying Methods 0.000 claims description 15
125000001309 chloro group Chemical group Cl* 0.000 claims description 14
229910052757 nitrogen Inorganic materials 0.000 claims description 14
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
125000005843 halogen group Chemical group 0.000 claims description 10
230000002363 herbicidal effect Effects 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
229940080818 propionamide Drugs 0.000 claims description 10
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 8
238000012360 testing method Methods 0.000 claims description 8
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
125000000547 substituted alkyl group Chemical group 0.000 claims description 7
239000004094 surface-active agent Substances 0.000 claims description 6
239000004563 wettable powder Substances 0.000 claims description 6
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims description 4
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
230000001419 dependent effect Effects 0.000 claims description 4
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 4
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 4
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 3
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QJQAMHYHNCADNR-UHFFFAOYSA-N n-methylpropanamide Chemical compound CCC(=O)NC QJQAMHYHNCADNR-UHFFFAOYSA-N 0.000 claims description 3
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MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 claims description 2
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238000000921 elemental analysis Methods 0.000 description 5
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IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 4
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VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
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UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
240000004713 Pisum sativum Species 0.000 description 1
235000010582 Pisum sativum Nutrition 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
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
229920001800 Shellac Polymers 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
AHAKIXFANJJJRC-UHFFFAOYSA-N aniline propanamide Chemical class CCC(N)=O.NC1=CC=CC=C1 AHAKIXFANJJJRC-UHFFFAOYSA-N 0.000 description 1
RAZBPJBBCGXPCO-UHFFFAOYSA-N aniline;propanoic acid Chemical compound CCC(O)=O.NC1=CC=CC=C1 RAZBPJBBCGXPCO-UHFFFAOYSA-N 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
235000003704 aspartic acid Nutrition 0.000 description 1
239000010426 asphalt Substances 0.000 description 1
235000013871 bee wax Nutrition 0.000 description 1
239000012166 beeswax Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
229940000635 beta-alanine Drugs 0.000 description 1
OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 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
DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 1
125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
235000012241 calcium silicate Nutrition 0.000 description 1
YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical class [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-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
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000002361 compost Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
244000038559 crop plants Species 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
239000012458 free base Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
239000003292 glue Substances 0.000 description 1
235000013922 glutamic acid Nutrition 0.000 description 1
239000004220 glutamic acid Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
125000006038 hexenyl group Chemical group 0.000 description 1
239000012943 hotmelt Substances 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
235000005772 leucine Nutrition 0.000 description 1
235000018977 lysine Nutrition 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
FFEARJCKVFRZRR-UHFFFAOYSA-N methionine Chemical compound CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 description 1
125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 description 1
239000012184 mineral wax Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003607 modifier Substances 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
239000012170 montan wax Substances 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
230000017066 negative regulation of growth Effects 0.000 description 1
239000000346 nonvolatile oil Substances 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
239000002245 particle Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
238000012545 processing Methods 0.000 description 1
RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000004208 shellac Substances 0.000 description 1
ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
235000013874 shellac Nutrition 0.000 description 1
229940113147 shellac Drugs 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
229910052814 silicon oxide Inorganic materials 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
235000019830 sodium polyphosphate Nutrition 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000005156 substituted alkylene group Chemical group 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003459 sulfonic acid esters Chemical class 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
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 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
235000014393 valine Nutrition 0.000 description 1
239000004474 valine Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000013585 weight reducing agent Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C243/34—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of a carbon skeleton further substituted by nitrogen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CH795867A 1966-06-08 1967-06-06 Herbicides Mittel CH501358A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB25473/66A GB1122043A (en)	1966-06-08	1966-06-08	Anilinoalkylcarboxamides and herbicidal compositions containing them

Publications (1)

Publication Number	Publication Date
CH501358A true CH501358A (de)	1971-01-15

Family

ID=10228289

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH795867A CH501358A (de)	1966-06-08	1967-06-06	Herbicides Mittel

Country Status (9)

Country	Link
BE (1)	BE699557A (fr)
CH (1)	CH501358A (fr)
DE (1)	DE1642337C3 (fr)
DK (1)	DK118797B (fr)
ES (1)	ES341454A1 (fr)
GB (1)	GB1122043A (fr)
NL (1)	NL159088B (fr)
OA (1)	OA02447A (fr)
SE (1)	SE359090B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4243819A (en) *	1978-02-16	1981-01-06	Zoecon Corporation	Substituted amino acids
EP0025616B1 (fr) *	1979-08-28	1983-11-30	Shell Internationale Researchmaatschappij B.V.	Un procédé pour détacher les fruits et/ou les feuilles
PE20220497A1 (es) *	2019-06-11	2022-04-07	Fortephest Ltd	Nuevos aminoacidos heterociclicos no codificantes (nchaa) y su uso como herbicidas

1966
- 1966-06-08 GB GB25473/66A patent/GB1122043A/en not_active Expired
1967
- 1967-06-05 OA OA52963A patent/OA02447A/fr unknown
- 1967-06-06 ES ES341454A patent/ES341454A1/es not_active Expired
- 1967-06-06 DE DE1642337A patent/DE1642337C3/de not_active Expired
- 1967-06-06 SE SE07887/67A patent/SE359090B/xx unknown
- 1967-06-06 BE BE699557D patent/BE699557A/xx unknown
- 1967-06-06 DK DK296367AA patent/DK118797B/da unknown
- 1967-06-06 CH CH795867A patent/CH501358A/de not_active IP Right Cessation
- 1967-06-07 NL NL6707890.A patent/NL159088B/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
DE1642337A1 (de)	1971-07-29
BE699557A (fr)	1967-12-06
DK118797B (da)	1970-10-05
DE1642337B2 (de)	1979-01-18
OA02447A (fr)	1970-05-05
ES341454A1 (es)	1968-12-01
NL6707890A (fr)	1967-12-11
SE359090B (fr)	1973-08-20
NL159088B (nl)	1979-01-15
DE1642337C3 (de)	1979-09-27
GB1122043A (en)	1968-07-31

Legal Events

Date	Code	Title	Description
1982-02-26	PL	Patent ceased

Publication	Publication Date	Title
DE1643527C3 (de)	1979-10-11	N,N-Disubstituierte Alanine und deren Verwendung als Herbicide
DE69431932T2 (de)	2003-12-24	Oligopeptide mit fungizider Aktivität
DD146177A5 (de)	1981-01-28	Verfahren zur herstellung von 2-chlor-6-nitroanilinen
DE2604989A1 (de)	1976-08-19	1,5-alkylen-3-aryl-hydantoin-derivate, verfahren zu ihrer herstellung und mittel mit herbizider und/oder fungizider wirkung
DE2643477A1 (de)	1977-04-07	Mikrobizide
EP0483062A2 (fr)	1992-04-29	Procédé pour la préparation de dérivés de la nitroguanidine
DE2905650A1 (de)	1980-08-21	Unkrautvernichtungsmittel
US3712805A (en)	1973-01-23	Weed control employing n,n-disubstituted amino acid herbicides
EP0368212A2 (fr)	1990-05-16	Agents herbicides, contenant des dérivés des acides 2-(4-hétéroaryloxy)- ou 2-(4-aryloxy)-phénoxy-acétiques ou -propioniques et/ou des dérivés de la cyclohexénone comme matières actives et des dérivés du naphtalène comme antidotes
CH501358A (de)	1971-01-15	Herbicides Mittel
DE2921002A1 (de)	1979-11-29	Cyclohexen-1,2-dicarbonsaeurediamide, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von unkraeutern
DE3783070T2 (de)	1993-05-13	Phenylharnstoffe.
DE2824126C2 (de)	1984-06-20	Tetrahydro-1,3,5-thiadiazin-4-on-Verbindungen
DE2526868C2 (de)	1984-09-20	N-Alken-(1)-yl-(1)-monohalogenacetamide, Verfahren zu deren Herstellung und diese enthaltende herbizides und pflanzenwachstums-regulierende Mittel
EP0294667B1 (fr)	1993-03-17	Dérivés d'acides (2-cyano-2-oximinoacétyl)-aminés
DE1921840A1 (de)	1969-11-20	Herbizide Mittel
EP0062254A1 (fr)	1982-10-13	Acétanilides substitués, procédé pour leur préparation et leur utilisation comme herbicides
EP0010692A1 (fr)	1980-05-14	N-m-Anilidocarbamates, herbicides les contenant et procédé pour leur préparation ainsi que procédé pour contrôler la croissance de plantes indésirables
DE1944525C3 (de)	1979-10-04	Anilinoalkanohydroxamsäureverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als herbicide Mittel
EP0108908A2 (fr)	1984-05-23	Benzotriazoles, leur préparation et application comme biocides
DE2234817A1 (de)	1974-01-31	Cyanphenoxyacetonitrile
DE2253027A1 (de)	1974-05-09	Fungizide mittel
DE2230076A1 (de)	1972-12-28	Verfahren zur Herstellung neuer heterocyclischer Stoffe
AT283045B (de)	1970-07-27	Herbizide Zubereitungen
DE2556938C2 (de)	1985-05-30	N,N-disubstituierte Alaninderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als herbicide Mittel