DE2902647A1 - N- eckige klammer auf (phosphinyl)- amino eckige klammer zu -thio- und neckige klammer auf (phosphinothioyl)amino eckige klammer zu- thio-methylcarbamate, verfahren zu ihrer herstellung, verwendung derselben zur bekaempfung von schadinsekten und zur bekaempfung von schadinsekten geeignete mittel - Google Patents
N- eckige klammer auf (phosphinyl)- amino eckige klammer zu -thio- und neckige klammer auf (phosphinothioyl)amino eckige klammer zu- thio-methylcarbamate, verfahren zu ihrer herstellung, verwendung derselben zur bekaempfung von schadinsekten und zur bekaempfung von schadinsekten geeignete mittelInfo
- Publication number
- DE2902647A1 DE2902647A1 DE19792902647 DE2902647A DE2902647A1 DE 2902647 A1 DE2902647 A1 DE 2902647A1 DE 19792902647 DE19792902647 DE 19792902647 DE 2902647 A DE2902647 A DE 2902647A DE 2902647 A1 DE2902647 A1 DE 2902647A1
- Authority
- DE
- Germany
- Prior art keywords
- radical
- methyl
- short
- amino
- formula
- 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.)
- Withdrawn
Links
- -1 (PHOSPHINYL) - AMINO Chemical class 0.000 title claims description 277
- 238000000034 method Methods 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 99
- 150000001875 compounds Chemical class 0.000 claims description 98
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 71
- GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims description 49
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 47
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 40
- 241000238631 Hexapoda Species 0.000 claims description 36
- YUKQRDCYNOVPGJ-UHFFFAOYSA-N thioacetamide Chemical compound CC(N)=S YUKQRDCYNOVPGJ-UHFFFAOYSA-N 0.000 claims description 36
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- 239000000203 mixture Substances 0.000 claims description 34
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 33
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 30
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- 229910052799 carbon Inorganic materials 0.000 claims description 25
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- 101150103491 Ptpmt1 gene Proteins 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 235000019764 Soybean Meal Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- 241000255993 Trichoplusia ni Species 0.000 description 1
- 240000006677 Vicia faba Species 0.000 description 1
- 235000010749 Vicia faba Nutrition 0.000 description 1
- 235000002098 Vicia faba var. major Nutrition 0.000 description 1
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- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- SIBASNOPCKGMTL-UHFFFAOYSA-N aminosulfanylmethylcarbamic acid Chemical compound NSCNC(O)=O SIBASNOPCKGMTL-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 229960000892 attapulgite Drugs 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
- 239000004305 biphenyl Substances 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
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters 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
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([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
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 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
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- GYKXQTKSWLAUIT-UHFFFAOYSA-N m-cumenyl methylcarbamate Chemical compound CNC(=O)OC1=CC=CC(C(C)C)=C1 GYKXQTKSWLAUIT-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- WWAHTNLMSOQBAN-UHFFFAOYSA-N methylaminomethyl carbamate Chemical compound C(N)(OCNC)=O WWAHTNLMSOQBAN-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- VSVLZHLRBOPTRA-UHFFFAOYSA-N n-cyclohexyl-5,5-dimethyl-2-sulfanylidene-1,3,2$l^{5}-dioxaphosphinan-2-amine Chemical compound O1CC(C)(C)COP1(=S)NC1CCCCC1 VSVLZHLRBOPTRA-UHFFFAOYSA-N 0.000 description 1
- RNNIVTRDSWWKQM-UHFFFAOYSA-N n-tert-butyl-5,5-dimethyl-2-sulfanylidene-1,3,2$l^{5}-dioxaphosphinan-2-amine Chemical compound CC(C)(C)NP1(=S)OCC(C)(C)CO1 RNNIVTRDSWWKQM-UHFFFAOYSA-N 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 231100000418 oral toxicity Toxicity 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000012430 organic reaction media Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical class O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000005549 size reduction Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2479—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1)
- C07F9/2483—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1) containing the structure P(=X)n-N-S (X = O, S, Se; n = 0, 1)
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus as a ring member
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657154—Cyclic esteramides of oxyacids of phosphorus
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87495978A | 1978-02-03 | 1978-02-03 | |
| US05/962,266 US4208409A (en) | 1977-02-04 | 1978-11-20 | N-[(phosphinyl or phosphinothioyl)amino]thio-methylcarbamates and pesticidal methods |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2902647A1 true DE2902647A1 (de) | 1979-08-09 |
Family
ID=27128362
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19792902647 Withdrawn DE2902647A1 (de) | 1978-02-03 | 1979-01-24 | N- eckige klammer auf (phosphinyl)- amino eckige klammer zu -thio- und neckige klammer auf (phosphinothioyl)amino eckige klammer zu- thio-methylcarbamate, verfahren zu ihrer herstellung, verwendung derselben zur bekaempfung von schadinsekten und zur bekaempfung von schadinsekten geeignete mittel |
Country Status (19)
| Country | Link |
|---|---|
| JP (1) | JPS5828879B2 (ja) |
| AU (1) | AU521661B2 (ja) |
| BR (1) | BR7900672A (ja) |
| CA (1) | CA1133918A (ja) |
| CH (1) | CH638815A5 (ja) |
| DD (1) | DD141779A5 (ja) |
| DE (1) | DE2902647A1 (ja) |
| DK (1) | DK45379A (ja) |
| EG (1) | EG14058A (ja) |
| ES (1) | ES477417A1 (ja) |
| FR (1) | FR2422673B1 (ja) |
| GB (1) | GB2015527B (ja) |
| HU (1) | HU184209B (ja) |
| IL (1) | IL56502A (ja) |
| IT (1) | IT1202876B (ja) |
| NL (1) | NL7900857A (ja) |
| OA (1) | OA06176A (ja) |
| PL (1) | PL115203B1 (ja) |
| YU (1) | YU24179A (ja) |
-
1979
- 1979-01-24 DE DE19792902647 patent/DE2902647A1/de not_active Withdrawn
- 1979-01-24 AU AU43607/79A patent/AU521661B2/en not_active Ceased
- 1979-01-25 IL IL56502A patent/IL56502A/xx unknown
- 1979-02-02 DD DD79210794A patent/DD141779A5/de unknown
- 1979-02-02 JP JP54011322A patent/JPS5828879B2/ja not_active Expired
- 1979-02-02 DK DK45379A patent/DK45379A/da not_active Application Discontinuation
- 1979-02-02 BR BR7900672A patent/BR7900672A/pt unknown
- 1979-02-02 NL NL7900857A patent/NL7900857A/xx not_active Application Discontinuation
- 1979-02-02 GB GB7903755A patent/GB2015527B/en not_active Expired
- 1979-02-02 YU YU00241/79A patent/YU24179A/xx unknown
- 1979-02-02 FR FR7902723A patent/FR2422673B1/fr not_active Expired
- 1979-02-02 ES ES477417A patent/ES477417A1/es not_active Expired
- 1979-02-02 IT IT19865/79A patent/IT1202876B/it active
- 1979-02-02 CH CH106979A patent/CH638815A5/de not_active IP Right Cessation
- 1979-02-02 CA CA320,756A patent/CA1133918A/en not_active Expired
- 1979-02-02 HU HU79UO153A patent/HU184209B/hu unknown
- 1979-02-03 EG EG69/79A patent/EG14058A/xx active
- 1979-02-03 OA OA56726A patent/OA06176A/xx unknown
- 1979-02-03 PL PL1979213213A patent/PL115203B1/pl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL56502A (en) | 1983-11-30 |
| AU521661B2 (en) | 1982-04-22 |
| HU184209B (en) | 1984-07-30 |
| ES477417A1 (es) | 1980-07-01 |
| GB2015527B (en) | 1982-04-21 |
| IT1202876B (it) | 1989-02-15 |
| YU24179A (en) | 1983-02-28 |
| JPS54115377A (en) | 1979-09-07 |
| PL115203B1 (en) | 1981-03-31 |
| NL7900857A (nl) | 1979-08-07 |
| DD141779A5 (de) | 1980-05-21 |
| CA1133918A (en) | 1982-10-19 |
| DK45379A (da) | 1979-08-04 |
| IT7919865A0 (it) | 1979-02-02 |
| BR7900672A (pt) | 1979-09-04 |
| JPS5828879B2 (ja) | 1983-06-18 |
| FR2422673A1 (fr) | 1979-11-09 |
| FR2422673B1 (fr) | 1985-06-28 |
| GB2015527A (en) | 1979-09-12 |
| OA06176A (fr) | 1981-06-30 |
| AU4360779A (en) | 1979-08-09 |
| CH638815A5 (de) | 1983-10-14 |
| PL213213A1 (ja) | 1980-02-25 |
| EG14058A (en) | 1984-06-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8128 | New person/name/address of the agent |
Representative=s name: HENKEL, G., DR.PHIL. FEILER, L., DR.RER.NAT. HAENZ |
|
| 8141 | Disposal/no request for examination |