DE2107698A1 - Verwendung eines Phenylharnstoffes zur Bekämpfung von Unkrautern in Weizen, Hafer, Roggen, Gersten, Reis und Baum wolle - Google Patents
Verwendung eines Phenylharnstoffes zur Bekämpfung von Unkrautern in Weizen, Hafer, Roggen, Gersten, Reis und Baum wolleInfo
- Publication number
- DE2107698A1 DE2107698A1 DE19712107698 DE2107698A DE2107698A1 DE 2107698 A1 DE2107698 A1 DE 2107698A1 DE 19712107698 DE19712107698 DE 19712107698 DE 2107698 A DE2107698 A DE 2107698A DE 2107698 A1 DE2107698 A1 DE 2107698A1
- Authority
- DE
- Germany
- Prior art keywords
- acid
- salts
- chloro
- urea
- cotton
- 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.)
- Pending
Links
- 241000196324 Embryophyta Species 0.000 title claims description 16
- 244000075850 Avena orientalis Species 0.000 title claims description 6
- 229920000742 Cotton Polymers 0.000 title claims description 6
- 244000299507 Gossypium hirsutum Species 0.000 title claims description 6
- 241000209140 Triticum Species 0.000 title claims description 6
- 235000021307 Triticum Nutrition 0.000 title claims description 6
- 235000007319 Avena orientalis Nutrition 0.000 title claims description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 title claims description 4
- 235000007164 Oryza sativa Nutrition 0.000 title claims description 4
- 244000082988 Secale cereale Species 0.000 title claims description 4
- 235000007238 Secale cereale Nutrition 0.000 title claims description 4
- 235000009566 rice Nutrition 0.000 title claims description 4
- 240000005979 Hordeum vulgare Species 0.000 title claims 2
- 240000007594 Oryza sativa Species 0.000 title claims 2
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 description 24
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 20
- 239000004480 active ingredient Substances 0.000 description 20
- 239000002253 acid Substances 0.000 description 15
- 239000004202 carbamide Substances 0.000 description 15
- -1 halogen fatty acids Chemical class 0.000 description 15
- 150000002148 esters Chemical class 0.000 description 13
- 235000013877 carbamide Nutrition 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
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- 239000008187 granular material Substances 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 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 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 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 3
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- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- AJBZENLMTKDAEK-UHFFFAOYSA-N 3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-4,9-diol Chemical compound CC12CCC(O)C(C)(C)C1CCC(C1(C)CC3O)(C)C2CCC1C1C3(C)CCC1C(=C)C AJBZENLMTKDAEK-UHFFFAOYSA-N 0.000 description 2
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- 241001303487 Digitaria <clam> Species 0.000 description 2
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 241001101998 Galium Species 0.000 description 2
- 241000207783 Ipomoea Species 0.000 description 2
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- 241000209117 Panicum Species 0.000 description 2
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 2
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 2
- 241000209048 Poa Species 0.000 description 2
- 240000006394 Sorghum bicolor Species 0.000 description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 2
- 240000006694 Stellaria media Species 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 229960000892 attapulgite Drugs 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000008029 eradication Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
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- 238000004519 manufacturing process Methods 0.000 description 2
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 229910052625 palygorskite Inorganic materials 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
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- 239000000454 talc Substances 0.000 description 2
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- 150000003918 triazines Chemical class 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- NJQRKFOZZUIMGW-UHFFFAOYSA-N 1,3,5-trichloro-2-(chloromethyl)benzene Chemical compound ClCC1=C(Cl)C=C(Cl)C=C1Cl NJQRKFOZZUIMGW-UHFFFAOYSA-N 0.000 description 1
- ICXVQQVHODGGRG-UHFFFAOYSA-N 1,3-dichlorourea Chemical compound ClNC(=O)NCl ICXVQQVHODGGRG-UHFFFAOYSA-N 0.000 description 1
- TWEBLPKRDRCUEH-UHFFFAOYSA-N 2,2-dichloropentanoic acid Chemical compound CCCC(Cl)(Cl)C(O)=O TWEBLPKRDRCUEH-UHFFFAOYSA-N 0.000 description 1
- NEBPTMCRLHKPOB-UHFFFAOYSA-N 2,2-diphenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)C1=CC=CC=C1 NEBPTMCRLHKPOB-UHFFFAOYSA-N 0.000 description 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- VYPKFHFVKFKHMK-UHFFFAOYSA-N 2-(1h-indol-2-yl)butanoic acid Chemical compound C1=CC=C2NC(C(C(O)=O)CC)=CC2=C1 VYPKFHFVKFKHMK-UHFFFAOYSA-N 0.000 description 1
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- KTOQRRDVVIDEAA-UHFFFAOYSA-N 2-methylpropane Chemical compound [CH2]C(C)C KTOQRRDVVIDEAA-UHFFFAOYSA-N 0.000 description 1
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- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 229940080818 propionamide Drugs 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid group Chemical class S(N)(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- 150000003470 sulfuric acid monoesters Chemical class 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 229940055764 triaz Drugs 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
- 229940066528 trichloroacetate Drugs 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH294470A CH537148A (de) | 1970-02-27 | 1970-02-27 | Verwendung von Phenylharnstoffen als selektive Herbizide |
| CH1392370A CH558141A (de) | 1970-09-21 | 1970-09-21 | Verwendung von phenylharnstoffen zur unkrautbekaempfung in getreidekulturen. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2107698A1 true DE2107698A1 (de) | 1971-09-16 |
Family
ID=25691782
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712107698 Pending DE2107698A1 (de) | 1970-02-27 | 1971-02-18 | Verwendung eines Phenylharnstoffes zur Bekämpfung von Unkrautern in Weizen, Hafer, Roggen, Gersten, Reis und Baum wolle |
| DE19712107699 Pending DE2107699A1 (de) | 1970-02-27 | 1971-02-18 | 4-Isopropyl-phenylharnstoffe, ihre Herstellung und ihre Verwendung zur Schädlingsbekämpfung |
| DE19712107774 Expired DE2107774C2 (de) | 1970-02-27 | 1971-02-18 | Verfahren zur selektiven Unkrautbekämpfung in Getreidekulturen |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712107699 Pending DE2107699A1 (de) | 1970-02-27 | 1971-02-18 | 4-Isopropyl-phenylharnstoffe, ihre Herstellung und ihre Verwendung zur Schädlingsbekämpfung |
| DE19712107774 Expired DE2107774C2 (de) | 1970-02-27 | 1971-02-18 | Verfahren zur selektiven Unkrautbekämpfung in Getreidekulturen |
Country Status (11)
| Country | Link |
|---|---|
| AU (1) | AU2590371A (enrdf_load_stackoverflow) |
| BE (3) | BE763515A (enrdf_load_stackoverflow) |
| CA (1) | CA1028867A (enrdf_load_stackoverflow) |
| CY (1) | CY979A (enrdf_load_stackoverflow) |
| DE (3) | DE2107698A1 (enrdf_load_stackoverflow) |
| FR (3) | FR2080809B1 (enrdf_load_stackoverflow) |
| GB (3) | GB1407586A (enrdf_load_stackoverflow) |
| IL (2) | IL36220A0 (enrdf_load_stackoverflow) |
| KE (1) | KE2909A (enrdf_load_stackoverflow) |
| NL (3) | NL7102616A (enrdf_load_stackoverflow) |
| RO (2) | RO57207A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2435747A1 (de) * | 1973-08-10 | 1975-02-13 | Lilly Industries Ltd | Stabile fluessige zubereitung mit herbicider wirkung und verfahren zu ihrer herstellung |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2039041A1 (de) * | 1970-08-06 | 1972-02-17 | Hoechst Ag | Herbizide Mittel |
| FR2180619B1 (enrdf_load_stackoverflow) * | 1972-04-21 | 1975-06-13 | Pepro | |
| FR2183625A1 (en) * | 1972-05-09 | 1973-12-21 | Pepro | N-4-isopropylphenyl-N',N'-dimethylurea herbicide - having synergistic action with mixts of neburon or linuron, esp for cereals |
| FR2215898B1 (enrdf_load_stackoverflow) * | 1973-02-02 | 1977-04-22 | Philagro Sa | |
| CH575208A5 (enrdf_load_stackoverflow) * | 1973-07-30 | 1976-05-14 | Ciba Geigy Ag | |
| DE2638402A1 (de) | 1975-09-05 | 1977-03-17 | Sandoz Ag | Organische verbindungen, ihre herstellung und verwendung |
| IT1123643B (it) | 1976-12-14 | 1986-04-30 | Montedison Spa | Uree ad azione insetticida e nematocida |
| CA1160072A (en) * | 1980-03-11 | 1984-01-10 | Shell Canada Limited | Herbicidal composition and method of combating undesired plant growth |
| MA19170A1 (fr) * | 1980-06-19 | 1981-12-31 | May & Baker Ltd | Procede pour la lutte contre les adventices a l'aide de (isopropyl-4-phenyl)-3 dimethyl-i,i-uree en combinaison avec le "s"(trichloro 2,3,3,alkyl thiocarbamate d'osopropyle . |
| CH652391A5 (de) * | 1982-01-15 | 1985-11-15 | Sandoz Ag | Harnstoff-derivate. |
| DE3222622A1 (de) * | 1982-06-11 | 1983-12-15 | Schering AG, 1000 Berlin und 4709 Bergkamen | Mittel zur entblaetterung von pflanzen mit synergistischer wirkung |
| US4749812A (en) * | 1985-05-27 | 1988-06-07 | Mitsui Toatsu Chemicals, Inc. | N-(3-chloro-4-isopropylphenyl) carboxamide derivative and selective herbicide |
| EP2052609A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| DE102008037621A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
| CN105532697B (zh) * | 2015-12-28 | 2018-04-27 | 江苏傲伦达科技实业股份有限公司 | 一种含有苄草丹和异丙隆的稻田除草组合物 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH242359A (fr) * | 1942-06-06 | 1946-05-15 | Bourdereau Alphonse Jacques | Film à réseau lenticulaire microscopique, procédé pour sa réalisation et mécanisme pour la mise en oeuvre dudit procédé. |
| US2655445A (en) * | 1949-12-06 | 1953-10-13 | Du Pont | 3-(halophenyl)-1-methyl-1-(methyl or ethyl) ureas and herbicidal compositions and methods employing same |
| US2655447A (en) * | 1952-02-14 | 1953-10-13 | Du Pont | Composition and method |
| NL236579A (enrdf_load_stackoverflow) * | 1958-02-01 | |||
| FR1251281A (fr) * | 1959-11-06 | 1961-01-20 | Du Pont | Composés complexes d'acides chlorobenzoïques et d'urées |
| US3228762A (en) * | 1960-10-03 | 1966-01-11 | Du Pont | Method of killing weeds |
| US3297425A (en) * | 1962-08-28 | 1967-01-10 | Du Pont | Herbicidal composition |
| CH424359A (de) * | 1963-01-29 | 1966-11-15 | Ciba Geigy | Schädlingsbekämpfungsmittel |
| FR1497868A (fr) * | 1965-10-28 | 1967-10-13 | Sandoz Sa | Procédé de lutte sélective contre les plantes adventices dans les cultures de céréales |
| IL31574A0 (en) * | 1968-02-13 | 1969-04-30 | Ciba Ltd | Use of certain ureas for combating weeds |
| FR2263590B1 (enrdf_load_stackoverflow) * | 1974-03-08 | 1976-12-10 | Alsthom Cgee |
-
1971
- 1971-02-17 IL IL36220A patent/IL36220A0/xx unknown
- 1971-02-17 IL IL36218A patent/IL36218A0/xx unknown
- 1971-02-18 DE DE19712107698 patent/DE2107698A1/de active Pending
- 1971-02-18 DE DE19712107699 patent/DE2107699A1/de active Pending
- 1971-02-18 DE DE19712107774 patent/DE2107774C2/de not_active Expired
- 1971-02-19 CA CA105,751A patent/CA1028867A/en not_active Expired
- 1971-02-25 FR FR7106517A patent/FR2080809B1/fr not_active Expired
- 1971-02-25 FR FR7106519A patent/FR2080810B1/fr not_active Expired
- 1971-02-25 FR FR7106518A patent/FR2079082A5/fr not_active Expired
- 1971-02-25 RO RO6606571A patent/RO57207A/ro unknown
- 1971-02-26 BE BE763515A patent/BE763515A/xx not_active IP Right Cessation
- 1971-02-26 NL NL7102616A patent/NL7102616A/xx unknown
- 1971-02-26 RO RO6608371A patent/RO57592A/ro unknown
- 1971-02-26 BE BE763516A patent/BE763516A/xx unknown
- 1971-02-26 BE BE763514A patent/BE763514A/xx unknown
- 1971-02-26 AU AU25903/71A patent/AU2590371A/en not_active Expired
- 1971-02-26 NL NL7102617A patent/NL7102617A/xx unknown
- 1971-02-26 NL NL7102615A patent/NL7102615A/xx unknown
- 1971-04-19 GB GB2262471A patent/GB1407586A/en not_active Expired
- 1971-04-19 CY CY97971A patent/CY979A/xx unknown
- 1971-04-19 GB GB5974873A patent/GB1407587A/en not_active Expired
- 1971-04-19 GB GB22623/71A patent/GB1293500A/en not_active Expired
-
1978
- 1978-12-07 KE KE290978A patent/KE2909A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2435747A1 (de) * | 1973-08-10 | 1975-02-13 | Lilly Industries Ltd | Stabile fluessige zubereitung mit herbicider wirkung und verfahren zu ihrer herstellung |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2590371A (en) | 1972-08-31 |
| KE2909A (en) | 1979-01-19 |
| CY979A (en) | 1979-03-23 |
| FR2080810B1 (enrdf_load_stackoverflow) | 1974-03-01 |
| NL7102616A (enrdf_load_stackoverflow) | 1971-08-31 |
| CA1028867A (en) | 1978-04-04 |
| IL36220A0 (en) | 1971-04-28 |
| RO57592A (enrdf_load_stackoverflow) | 1975-02-15 |
| FR2080810A1 (enrdf_load_stackoverflow) | 1971-11-19 |
| BE763516A (fr) | 1971-08-26 |
| BE763514A (fr) | 1971-08-26 |
| IL36218A0 (en) | 1971-04-28 |
| GB1407587A (en) | 1975-09-24 |
| RO57207A (enrdf_load_stackoverflow) | 1975-01-15 |
| FR2080809B1 (enrdf_load_stackoverflow) | 1974-03-01 |
| NL7102617A (enrdf_load_stackoverflow) | 1971-08-31 |
| GB1407586A (en) | 1975-09-24 |
| NL7102615A (enrdf_load_stackoverflow) | 1971-08-31 |
| DE2107774C2 (de) | 1990-03-29 |
| FR2079082A5 (enrdf_load_stackoverflow) | 1971-11-05 |
| FR2080809A1 (enrdf_load_stackoverflow) | 1971-11-19 |
| GB1293500A (en) | 1972-10-18 |
| DE2107699A1 (de) | 1971-09-16 |
| BE763515A (fr) | 1971-08-26 |
| DE2107774A1 (de) | 1971-09-16 |
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Legal Events
| Date | Code | Title | Description |
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| OHN | Withdrawal |