DE1197676B - Totalherbizid - Google Patents
TotalherbizidInfo
- Publication number
- DE1197676B DE1197676B DEB75382A DEB0075382A DE1197676B DE 1197676 B DE1197676 B DE 1197676B DE B75382 A DEB75382 A DE B75382A DE B0075382 A DEB0075382 A DE B0075382A DE 1197676 B DE1197676 B DE 1197676B
- Authority
- DE
- Germany
- Prior art keywords
- radical
- phenyl
- spp
- total herbicide
- total
- 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.)
- Granted
Links
- 230000002363 herbicidal effect Effects 0.000 title claims description 6
- 239000004009 herbicide Substances 0.000 title claims description 3
- -1 alkyl radical Chemical class 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- TUCNEACPLKLKNU-UHFFFAOYSA-N acetyl Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- 241000219873 Vicia Species 0.000 description 9
- 239000004480 active ingredient Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 240000006694 Stellaria media Species 0.000 description 6
- 235000009108 Urtica dioica Nutrition 0.000 description 6
- 240000001592 Amaranthus caudatus Species 0.000 description 5
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 5
- 235000007320 Avena fatua Nutrition 0.000 description 5
- 240000006122 Chenopodium album Species 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 5
- 244000292693 Poa annua Species 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 244000075850 Avena orientalis Species 0.000 description 4
- 244000056139 Brassica cretica Species 0.000 description 4
- 235000003351 Brassica cretica Nutrition 0.000 description 4
- 235000003343 Brassica rupestris Nutrition 0.000 description 4
- 240000004153 Hibiscus sabdariffa Species 0.000 description 4
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 4
- 244000292697 Polygonum aviculare Species 0.000 description 4
- 235000006386 Polygonum aviculare Nutrition 0.000 description 4
- 235000005291 Rumex acetosa Nutrition 0.000 description 4
- 244000274883 Urtica dioica Species 0.000 description 4
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 235000010460 mustard Nutrition 0.000 description 4
- 235000003513 sheep sorrel Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000011498 Chenopodium album var missouriense Nutrition 0.000 description 3
- 235000013328 Chenopodium album var. album Nutrition 0.000 description 3
- 235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 3
- 235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 3
- 235000013012 Chenopodium album var. striatum Nutrition 0.000 description 3
- 240000004585 Dactylis glomerata Species 0.000 description 3
- 240000005702 Galium aparine Species 0.000 description 3
- 235000014820 Galium aparine Nutrition 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000008635 plant growth Effects 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 244000307697 Agrimonia eupatoria Species 0.000 description 2
- 235000016626 Agrimonia eupatoria Nutrition 0.000 description 2
- 241001621841 Alopecurus myosuroides Species 0.000 description 2
- 241000209764 Avena fatua Species 0.000 description 2
- 235000006463 Brassica alba Nutrition 0.000 description 2
- 244000140786 Brassica hirta 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
- 235000009344 Chenopodium album Nutrition 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241001456088 Hesperocnide Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 241000221024 Mercurialis Species 0.000 description 2
- 241000205407 Polygonum Species 0.000 description 2
- 241000219053 Rumex Species 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 229920005552 sodium lignosulfonate Polymers 0.000 description 2
- PRNVZGWKUODJPE-UHFFFAOYSA-N 4,5-dimethoxy-2-phenyl-1,5-dihydropyridazin-6-one Chemical compound C1(=CC=CC=C1)N1NC(C(C(=C1)OC)OC)=O PRNVZGWKUODJPE-UHFFFAOYSA-N 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241000219312 Chenopodium Species 0.000 description 1
- 235000004385 Conyza canadensis Nutrition 0.000 description 1
- 244000045393 Heracleum sphondylium Species 0.000 description 1
- 235000007239 Heracleum sphondylium Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 244000207740 Lemna minor Species 0.000 description 1
- 235000006439 Lemna minor Nutrition 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000001855 Portulaca oleracea Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 244000152045 Themeda triandra Species 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 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
- 238000009835 boiling Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 239000012876 carrier material Substances 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
- 239000003245 coal Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 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
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229910052500 inorganic mineral Chemical class 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
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 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
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
- C07D237/14—Oxygen atoms
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
- C07D237/14—Oxygen atoms
- C07D237/16—Two oxygen atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL126015D NL126015C (en, 2012) | 1964-02-12 | ||
DEB75382A DE1197676B (de) | 1964-02-12 | 1964-02-12 | Totalherbizid |
GB4262/65A GB1088612A (en) | 1964-02-12 | 1965-02-01 | Pyridazone derivatives |
US429879A US3326660A (en) | 1964-02-12 | 1965-02-02 | Pyridazones and method for controlling vegetation |
DK62065AA DK109006C (da) | 1964-02-12 | 1965-02-06 | Middel til bekæmpelse af uonsket plantevækst og fremgangsmåder til fremstilling af pyridazonderivater til anvendelse i midlet. |
BE659466D BE659466A (en, 2012) | 1964-02-12 | 1965-02-09 | |
SE01795/65A SE334618B (en, 2012) | 1964-02-12 | 1965-02-11 | |
BR167136/65A BR6567136D0 (pt) | 1964-02-12 | 1965-02-12 | Composicoes herbicidas concentradas |
NL6501789A NL6501789A (en, 2012) | 1964-02-12 | 1965-02-12 | |
CS965*BA CS150160B2 (en, 2012) | 1964-02-12 | 1965-02-12 | |
FR5338A FR1439067A (fr) | 1964-02-12 | 1965-02-12 | Agents pour empêcher la croissance de plantes indésirables |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB75382A DE1197676B (de) | 1964-02-12 | 1964-02-12 | Totalherbizid |
Publications (2)
Publication Number | Publication Date |
---|---|
DE1197676B true DE1197676B (de) | 1965-07-29 |
DE1197676C2 DE1197676C2 (en, 2012) | 1966-04-21 |
Family
ID=6978635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEB75382A Granted DE1197676B (de) | 1964-02-12 | 1964-02-12 | Totalherbizid |
Country Status (10)
Country | Link |
---|---|
US (1) | US3326660A (en, 2012) |
BE (1) | BE659466A (en, 2012) |
BR (1) | BR6567136D0 (en, 2012) |
CS (1) | CS150160B2 (en, 2012) |
DE (1) | DE1197676B (en, 2012) |
DK (1) | DK109006C (en, 2012) |
FR (1) | FR1439067A (en, 2012) |
GB (1) | GB1088612A (en, 2012) |
NL (2) | NL6501789A (en, 2012) |
SE (1) | SE334618B (en, 2012) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4523946A (en) * | 1982-01-28 | 1985-06-18 | Basf Aktiengesellschaft | Substituted 4,5-dimethoxypyridazones and their use for controlling undesirable plant growth |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4661145A (en) * | 1977-03-10 | 1987-04-28 | Rohm And Haas Company | Plant growth regulating 1-aryl-1,4-dihydro-4-oxo(thio)-pyridazines |
DE2808193A1 (de) * | 1978-02-25 | 1979-09-06 | Basf Ag | Pyridazon-verbindungen |
DE3013267A1 (de) | 1980-04-05 | 1981-10-15 | Basf Ag, 6700 Ludwigshafen | Substituierte pyridazone, verfahren zu ihrer herstellung, diese enthaltende herbizide und ihre anwendung als herbizide |
US5062880A (en) * | 1980-10-03 | 1991-11-05 | Monsanto Company | 1-aryl-1,4-dihydro-4-oxo-5-carboxypyridazine derivatives and their use as plant growth regulators and hybridizing agents |
US4707181A (en) * | 1980-10-03 | 1987-11-17 | Rohm And Haas Company | 1-aryl-1,4-dihydro-4-oxo-3,5-dicarboxypyridazine derivatives and their use as plant growth regulators and hybridizing agents |
US4732603A (en) * | 1980-10-03 | 1988-03-22 | Rohm And Haas Company | 1-aryl-1,4-dihydro-4-oxo-5-carboxypyridazine derivatives and their use as plant growth regulators and hybridizing agents |
DE3321007A1 (de) * | 1983-06-10 | 1984-12-13 | Basf Ag, 6700 Ludwigshafen | Substituierte 4,5-dimethoxypyridazone, verfahren zu ihrer herstellung, diese enthaltende herbizide und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses als herbizide |
DE3807896A1 (de) * | 1988-03-10 | 1989-09-21 | Basf Ag | 2-phenylpyridazin-3-on-verbindungen, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
CL2008003785A1 (es) * | 2007-12-21 | 2009-10-09 | Du Pont | Compuestos derivados de piridazina; composiciones herbicidas que comprenden a dichos compuestos; y método para controlar el crecimiento de la vegetación indeseada. |
US20120149710A1 (en) * | 2009-08-24 | 2012-06-14 | The Regents Of The University Of California | Sortase a inhibitors |
-
0
- NL NL126015D patent/NL126015C/xx active
-
1964
- 1964-02-12 DE DEB75382A patent/DE1197676B/de active Granted
-
1965
- 1965-02-01 GB GB4262/65A patent/GB1088612A/en not_active Expired
- 1965-02-02 US US429879A patent/US3326660A/en not_active Expired - Lifetime
- 1965-02-06 DK DK62065AA patent/DK109006C/da active
- 1965-02-09 BE BE659466D patent/BE659466A/xx unknown
- 1965-02-11 SE SE01795/65A patent/SE334618B/xx unknown
- 1965-02-12 BR BR167136/65A patent/BR6567136D0/pt unknown
- 1965-02-12 NL NL6501789A patent/NL6501789A/xx unknown
- 1965-02-12 CS CS965*BA patent/CS150160B2/cs unknown
- 1965-02-12 FR FR5338A patent/FR1439067A/fr not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4523946A (en) * | 1982-01-28 | 1985-06-18 | Basf Aktiengesellschaft | Substituted 4,5-dimethoxypyridazones and their use for controlling undesirable plant growth |
Also Published As
Publication number | Publication date |
---|---|
BR6567136D0 (pt) | 1973-07-24 |
SE334618B (en, 2012) | 1971-05-03 |
FR1439067A (fr) | 1966-05-20 |
DK109006C (da) | 1968-03-04 |
BE659466A (en, 2012) | 1965-08-09 |
NL6501789A (en, 2012) | 1965-08-13 |
CS150160B2 (en, 2012) | 1973-09-04 |
DE1197676C2 (en, 2012) | 1966-04-21 |
GB1088612A (en) | 1967-10-25 |
US3326660A (en) | 1967-06-20 |
NL126015C (en, 2012) |
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