DE2304609A1 - 3-halogen-5-alkyl-delta hoch 2-thiadiazolin-4-one und deren verwendung als pestizide - Google Patents
3-halogen-5-alkyl-delta hoch 2-thiadiazolin-4-one und deren verwendung als pestizideInfo
- Publication number
- DE2304609A1 DE2304609A1 DE2304609A DE2304609A DE2304609A1 DE 2304609 A1 DE2304609 A1 DE 2304609A1 DE 2304609 A DE2304609 A DE 2304609A DE 2304609 A DE2304609 A DE 2304609A DE 2304609 A1 DE2304609 A1 DE 2304609A1
- Authority
- DE
- Germany
- Prior art keywords
- thiadiazolin
- chloro
- alkyl
- compound according
- ethyl
- 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
- 239000000575 pesticide Substances 0.000 title description 4
- HSBAPCKJUUSMLH-UHFFFAOYSA-N thiadiazol-4-one Chemical compound O=C1CSN=N1 HSBAPCKJUUSMLH-UHFFFAOYSA-N 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 14
- 241000894006 Bacteria Species 0.000 claims description 13
- 230000000844 anti-bacterial effect Effects 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 238000011160 research Methods 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 6
- 230000001580 bacterial effect Effects 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 239000000370 acceptor Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 239000003053 toxin Substances 0.000 description 4
- 231100000765 toxin Toxicity 0.000 description 4
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 150000004868 1,2,5-thiadiazoles Chemical class 0.000 description 2
- LLBZPESJRQGYMB-UHFFFAOYSA-N 4-one Natural products O1C(C(=O)CC)CC(C)C11C2(C)CCC(C3(C)C(C(C)(CO)C(OC4C(C(O)C(O)C(COC5C(C(O)C(O)CO5)OC5C(C(OC6C(C(O)C(O)C(CO)O6)O)C(O)C(CO)O5)OC5C(C(O)C(O)C(C)O5)O)O4)O)CC3)CC3)=C3C2(C)CC1 LLBZPESJRQGYMB-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- 241000589158 Agrobacterium Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- 241000588698 Erwinia Species 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 241000589615 Pseudomonas syringae Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 241000567019 Xanthomonas vesicatoria Species 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 239000003708 ampul Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000008223 sterile water Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- SEPPVOUBHWNCAW-FNORWQNLSA-N (E)-4-oxonon-2-enal Chemical compound CCCCCC(=O)\C=C\C=O SEPPVOUBHWNCAW-FNORWQNLSA-N 0.000 description 1
- WEEMDRWIKYCTQM-UHFFFAOYSA-N 2,6-dimethoxybenzenecarbothioamide Chemical compound COC1=CC=CC(OC)=C1C(N)=S WEEMDRWIKYCTQM-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- WEDKTMOIKOKBSH-UHFFFAOYSA-N 4,5-dihydrothiadiazole Chemical compound C1CN=NS1 WEDKTMOIKOKBSH-UHFFFAOYSA-N 0.000 description 1
- 108010023063 Bacto-peptone Proteins 0.000 description 1
- 239000005745 Captan Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000227653 Lycopersicon Species 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000521936 Pseudomonas amygdali pv. lachrymans Species 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 241000194062 Xanthomonas phaseoli Species 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
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- -1 alkyl radical Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 229940117949 captan Drugs 0.000 description 1
- YDVJBLJCSLVMSY-UHFFFAOYSA-N carbamoyl cyanide Chemical compound NC(=O)C#N YDVJBLJCSLVMSY-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- AEIVXVKOOYOIPJ-UHFFFAOYSA-N n-cyano-n-methylformamide Chemical compound O=CN(C)C#N AEIVXVKOOYOIPJ-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000013558 reference substance Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229960002385 streptomycin sulfate Drugs 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/10—1,2,5-Thiadiazoles; Hydrogenated 1,2,5-thiadiazoles
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23296172A | 1972-03-08 | 1972-03-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2304609A1 true DE2304609A1 (de) | 1973-09-20 |
Family
ID=22875275
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2304609A Pending DE2304609A1 (de) | 1972-03-08 | 1973-01-31 | 3-halogen-5-alkyl-delta hoch 2-thiadiazolin-4-one und deren verwendung als pestizide |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3763176A (OSRAM) |
| JP (1) | JPS4912034A (OSRAM) |
| CA (1) | CA996564A (OSRAM) |
| DE (1) | DE2304609A1 (OSRAM) |
| FR (1) | FR2174892B1 (OSRAM) |
| GB (1) | GB1373334A (OSRAM) |
| IT (1) | IT981216B (OSRAM) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3854000A (en) * | 1972-03-08 | 1974-12-10 | Chevron Res | Bactericidal 3-halo-5-alkyl-{66 {11 -thiadiazolin-4-one |
| US4093618A (en) * | 1973-09-25 | 1978-06-06 | Ciba-Geigy Corporation | Amides of 2,4,6-trialkyl-3-hydroxy-phenylalkanoic acids |
| US4094986A (en) * | 1976-05-07 | 1978-06-13 | M. S. & D. (I.A.) Corp. | 2-r-substituted-1,2,5-thiadiazole-3-one antimicrobials |
| US4431655A (en) * | 1980-04-21 | 1984-02-14 | Merck & Co., Inc. | 2,4-Disubstituted-1,2,5-thiadiazol-3(2H)-one antimicrobials |
| US4362877A (en) * | 1980-04-21 | 1982-12-07 | Merck & Co., Inc. | 2,4-Disubstituted-1,2,5-thiadiazol-3(2H)-one antimicrobials |
| US4402959A (en) * | 1980-06-02 | 1983-09-06 | Merck & Co., Inc. | Antimicrobial compositions |
| US4517186A (en) * | 1982-09-30 | 1985-05-14 | Merck & Co., Inc. | 2-Amino-3,5-dicyano-6-(substituted)pyrazine antimicrobial compounds |
| US4518599A (en) * | 1982-09-30 | 1985-05-21 | Merck & Co., Inc. | 2-Amino-3-cyano-5-halo-6-(substituted)pyrazine |
| US4442097A (en) * | 1982-12-27 | 1984-04-10 | Merck & Co., Inc. | 3-Acyl-2-(substituted) amino-5-halo-6-(substituted) pyrazine antimicrobial compounds, compositions and use |
| US4442096A (en) * | 1982-12-27 | 1984-04-10 | Merck & Co., Inc. | 2-(Substituted)amino-3-cyano-5-halo-6-(substituted)-pyrazine antimicrobial compounds, compositions and use |
| US4481202A (en) * | 1982-12-27 | 1984-11-06 | Merek & Co., Inc. | 2-Amino-3-carboxylate-5-halo-6-(substituted)pyrazine antimicrobial compounds |
| US4512991A (en) * | 1982-12-27 | 1985-04-23 | Merck & Co., Inc. | 3-Acyl-2-amino-5-halo-6-(substituted)pyrazine antimicrobial compounds |
| US4507299A (en) * | 1982-12-27 | 1985-03-26 | Merck & Co., Inc. | N-[2-amino-5-halo-6-(substituted)-3-pyrazinyl)-methylene]amine antimicrobial compounds |
| US4442095A (en) * | 1982-12-27 | 1984-04-10 | Merck & Co., Inc. | N-[(5-Halo-2,6-(substituted)pyrazinyl)methylene]amine antimicrobial compounds, compositions and use |
| JPS607176A (ja) * | 1983-06-27 | 1985-01-14 | Nippon Texas Instr Kk | 半導体装置 |
-
1972
- 1972-03-08 US US00232961A patent/US3763176A/en not_active Expired - Lifetime
-
1973
- 1973-01-11 CA CA161,074A patent/CA996564A/en not_active Expired
- 1973-01-31 DE DE2304609A patent/DE2304609A1/de active Pending
- 1973-02-28 GB GB983573A patent/GB1373334A/en not_active Expired
- 1973-03-01 FR FR7307346A patent/FR2174892B1/fr not_active Expired
- 1973-03-06 JP JP48026496A patent/JPS4912034A/ja active Pending
- 1973-03-08 IT IT21329/73A patent/IT981216B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| IT981216B (it) | 1974-10-10 |
| GB1373334A (en) | 1974-11-13 |
| FR2174892B1 (OSRAM) | 1977-02-11 |
| CA996564A (en) | 1976-09-07 |
| FR2174892A1 (OSRAM) | 1973-10-19 |
| US3763176A (en) | 1973-10-02 |
| JPS4912034A (OSRAM) | 1974-02-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2304609A1 (de) | 3-halogen-5-alkyl-delta hoch 2-thiadiazolin-4-one und deren verwendung als pestizide | |
| DE1792776A1 (de) | Schaedlingsbekaempfungsmittel mit insektizider, mikrobizider und herbizider wirkung | |
| DE1812497C3 (de) | N-Phosphinothioyl-thiomethyl-carbonyl-piperidine, Verfahren zu ihrer Herstellung und diese enthaltende Mittel | |
| DE1542715A1 (de) | Schaedlingsbekaempfungsmittel | |
| DE1218210B (de) | Fungizide Mittel mit herbizider und nematozider Wirkung | |
| DE2156447A1 (de) | Neue Amidothionophosphonsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide | |
| DE2344010A1 (de) | Neue 5-nitrochinolin-derivate, verfahren zur herstellung und diese enthaltende zusammensetzungen | |
| DE2408863A1 (de) | 2-chloraethanphosphonsaeurederivate | |
| DE2166953A1 (de) | Antimikrobielles mittel | |
| DE2159565A1 (de) | Isoxazolinon-Verbindungen, Verfahren zu deren Herstellung und deren Anwendung als Verbindungen für die Landwirtschaft | |
| DE2320371A1 (de) | Thiophosphonsaeureester | |
| DE2515773A1 (de) | Halogen-bis-(thiocyanatomethylthio)- pyridine, sowie verfahren zur herstellung derselben | |
| AT267960B (de) | Bekämpfung von Unkräutern | |
| DE2426971C2 (de) | Phenylendiamin-derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Pestizide | |
| DE1542715C (de) | Schädlingsbekämpfungsmittel | |
| AT250987B (de) | Verfahren zur Herstellung von neuen Zinnkomplexsalzen | |
| DE953125C (de) | Mittel zur Bekaempfung von Mikroorganismen, wie Pilzen (Fungi), Bakterien und Protozoen | |
| DE1670457A1 (de) | Neue Carbamate und Solche enthaltende Schaedlingsbekaempfungsmittel | |
| DE1212515B (de) | Verfahren zur Herstellung von Halogenallylestern der Methanthiosulfonsaeure | |
| DE1542956A1 (de) | Herbicide | |
| DE2052234C3 (de) | Verwendung von 2-Mercaptopyridin-1-oxidaminsalzen als anthnikrobielles Mittel in Brenn- und Treibstoffen | |
| AT272336B (de) | Verfahren zur Herstellung von neuen Tetrahalogenäthylthiopyrazolen | |
| DE2031236C3 (de) | Neue 10,11- Dihydrodibenzo (b,f) azepinderivate, ihre Herstellung und fungizide Zusammensetzungen | |
| AT233319B (de) | Fungizide Mittel | |
| DE1225190B (de) | Verfahren zur Herstellung von Naphthalin-1, 4, 5, 8-tetracarbonsaeurediimidderivaten |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| OHN | Withdrawal |