DE2241560C3 - Herbizide Mittel auf Basis von Benzophenonderivaten - Google Patents
Herbizide Mittel auf Basis von BenzophenonderivatenInfo
- Publication number
- DE2241560C3 DE2241560C3 DE2241560A DE2241560A DE2241560C3 DE 2241560 C3 DE2241560 C3 DE 2241560C3 DE 2241560 A DE2241560 A DE 2241560A DE 2241560 A DE2241560 A DE 2241560A DE 2241560 C3 DE2241560 C3 DE 2241560C3
- Authority
- DE
- Germany
- Prior art keywords
- general formula
- benzophenone derivatives
- parts
- compound
- herbicidal agents
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 150000008366 benzophenones Chemical class 0.000 title claims description 14
- 239000004009 herbicide Substances 0.000 title claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000005648 plant growth regulator Substances 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 21
- 150000001875 compounds Chemical class 0.000 description 15
- 239000000203 mixture Substances 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 230000002363 herbicidal effect Effects 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 240000003173 Drymaria cordata Species 0.000 description 3
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 208000006278 hypochromic anemia Diseases 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- QAHFOPIILNICLA-UHFFFAOYSA-N Diphenamid Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 QAHFOPIILNICLA-UHFFFAOYSA-N 0.000 description 2
- 241001523358 Glyceria Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 240000004658 Medicago sativa Species 0.000 description 2
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 2
- 240000003768 Solanum lycopersicum Species 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- -1 dusts Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012433 hydrogen halide Substances 0.000 description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000003267 mannagrass Nutrition 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- KDYYFNARCRZVDG-UHFFFAOYSA-N (4-methoxy-2-methylphenyl)-phenylmethanone Chemical compound CC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 KDYYFNARCRZVDG-UHFFFAOYSA-N 0.000 description 1
- XKQLZRYPUPMZHI-UHFFFAOYSA-N (4-methoxy-3-methylphenyl)-phenylmethanone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC=C1 XKQLZRYPUPMZHI-UHFFFAOYSA-N 0.000 description 1
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical class C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 1
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 240000001592 Amaranthus caudatus Species 0.000 description 1
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 1
- 240000008399 Barbarea vulgaris Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000011305 Capsella bursa pastoris Nutrition 0.000 description 1
- 240000008867 Capsella bursa-pastoris Species 0.000 description 1
- 235000008473 Cardamine hirsuta Nutrition 0.000 description 1
- 235000014412 Cardamine oligosperma Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 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 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 235000009198 Lamium amplexicaule Nutrition 0.000 description 1
- 244000303225 Lamium amplexicaule Species 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 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
- 241001660497 Piptatherum thomasii Species 0.000 description 1
- 244000292693 Poa annua Species 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003899 bactericide agent 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
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 235000013339 cereals Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012050 conventional carrier Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- GQDAQMBBGHMTQX-UHFFFAOYSA-N dihydroxy-propylsulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CCCSP(O)(O)=S GQDAQMBBGHMTQX-UHFFFAOYSA-N 0.000 description 1
- LRCFXGAMWKDGLA-UHFFFAOYSA-N dioxosilane;hydrate Chemical compound O.O=[Si]=O LRCFXGAMWKDGLA-UHFFFAOYSA-N 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 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 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229960004029 silicic acid Drugs 0.000 description 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
-
- 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
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP46064658A JPS515446B2 (https=) | 1971-08-24 | 1971-08-24 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2241560A1 DE2241560A1 (de) | 1973-03-08 |
| DE2241560B2 DE2241560B2 (de) | 1980-09-11 |
| DE2241560C3 true DE2241560C3 (de) | 1981-04-30 |
Family
ID=13264524
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2241560A Expired DE2241560C3 (de) | 1971-08-24 | 1972-08-24 | Herbizide Mittel auf Basis von Benzophenonderivaten |
| DE2265535A Expired DE2265535C3 (de) | 1971-08-24 | 1972-08-24 | Herbizide Mittel und ihre Verwendung als Pflanzenwuchsregler |
| DE2265418A Expired DE2265418C2 (de) | 1971-08-24 | 1972-08-24 | Benzophenonderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenwuchsregler |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2265535A Expired DE2265535C3 (de) | 1971-08-24 | 1972-08-24 | Herbizide Mittel und ihre Verwendung als Pflanzenwuchsregler |
| DE2265418A Expired DE2265418C2 (de) | 1971-08-24 | 1972-08-24 | Benzophenonderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenwuchsregler |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US3873304A (https=) |
| JP (1) | JPS515446B2 (https=) |
| BE (1) | BE787938A (https=) |
| BR (1) | BR7205728D0 (https=) |
| CA (1) | CA1025688A (https=) |
| CH (1) | CH574706A5 (https=) |
| DE (3) | DE2241560C3 (https=) |
| FR (1) | FR2150492B1 (https=) |
| GB (1) | GB1355926A (https=) |
| IL (1) | IL40159A (https=) |
| IT (1) | IT964243B (https=) |
| NL (1) | NL7211551A (https=) |
| PH (1) | PH10246A (https=) |
| SU (1) | SU516341A3 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4102672A (en) * | 1973-10-19 | 1978-07-25 | Ajinomoto Co. Inc. | Herbicidal composition of amino acid higher alkyl ester type and method for controlling weeds |
| US3954875A (en) * | 1973-12-26 | 1976-05-04 | Rohm And Haas Company | Benzophenone herbicides |
| FR2292467A1 (fr) * | 1974-11-28 | 1976-06-25 | Roussel Uclaf | Nouveaux derives de la benzophenone, leur procede de preparation et leur application comme medicament |
| GB2102420B (en) * | 1981-07-08 | 1985-08-21 | Raychem Corp | Preparation of aromatic ketones |
| JPS60235369A (ja) * | 1984-05-08 | 1985-11-22 | Yuasa Battery Co Ltd | ナトリウム−硫黄電池 |
| GB9620202D0 (en) * | 1996-09-27 | 1996-11-13 | Rhone Poulenc Agriculture | New herbicides |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2671016A (en) * | 1951-10-23 | 1954-03-02 | Monsanto Chemicals | Herbicidal compositions |
| US3013079A (en) * | 1957-01-18 | 1961-12-12 | Donald E Pearson | Ring halogenation of aromatic carbonyl compounds |
| US3086988A (en) * | 1961-07-12 | 1963-04-23 | Dow Chemical Co | 2-hydroxy-4-(2-hydroxyalkoxy) benzophenones and their lower alkanoic acid esters |
| US3495970A (en) * | 1969-01-08 | 1970-02-17 | Hazzard John | Herbicidal composition and method |
-
0
- BE BE787938D patent/BE787938A/xx unknown
-
1971
- 1971-08-24 JP JP46064658A patent/JPS515446B2/ja not_active Expired
-
1972
- 1972-08-18 IL IL40159A patent/IL40159A/xx unknown
- 1972-08-21 US US282270A patent/US3873304A/en not_active Expired - Lifetime
- 1972-08-22 GB GB3911072A patent/GB1355926A/en not_active Expired
- 1972-08-22 BR BR5728/72A patent/BR7205728D0/pt unknown
- 1972-08-22 CH CH1243772A patent/CH574706A5/xx not_active IP Right Cessation
- 1972-08-23 SU SU1824103A patent/SU516341A3/ru active
- 1972-08-24 CA CA150,094A patent/CA1025688A/en not_active Expired
- 1972-08-24 DE DE2241560A patent/DE2241560C3/de not_active Expired
- 1972-08-24 IT IT28483/72A patent/IT964243B/it active
- 1972-08-24 PH PH13832A patent/PH10246A/en unknown
- 1972-08-24 DE DE2265535A patent/DE2265535C3/de not_active Expired
- 1972-08-24 NL NL7211551A patent/NL7211551A/xx not_active Application Discontinuation
- 1972-08-24 DE DE2265418A patent/DE2265418C2/de not_active Expired
- 1972-08-24 FR FR7230173A patent/FR2150492B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CA1025688A (en) | 1978-02-07 |
| DE2265418C2 (de) | 1979-10-25 |
| GB1355926A (en) | 1974-06-12 |
| IT964243B (it) | 1974-01-21 |
| IL40159A (en) | 1975-11-25 |
| PH10246A (en) | 1976-10-14 |
| IL40159A0 (en) | 1972-10-29 |
| SU516341A3 (ru) | 1976-05-30 |
| NL7211551A (https=) | 1973-02-27 |
| JPS4828627A (https=) | 1973-04-16 |
| DE2265535C3 (de) | 1982-04-29 |
| CH574706A5 (https=) | 1976-04-30 |
| DE2265535B2 (de) | 1981-07-16 |
| US3873304A (en) | 1975-03-25 |
| DE2241560B2 (de) | 1980-09-11 |
| DE2265418B1 (de) | 1979-03-08 |
| DE2241560A1 (de) | 1973-03-08 |
| FR2150492A1 (https=) | 1973-04-06 |
| JPS515446B2 (https=) | 1976-02-20 |
| FR2150492B1 (https=) | 1975-01-03 |
| BE787938A (fr) | 1973-02-26 |
| BR7205728D0 (pt) | 1974-10-22 |
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