CH564551A5 - - Google Patents
Info
- Publication number
- CH564551A5 CH564551A5 CH1410574A CH1410574A CH564551A5 CH 564551 A5 CH564551 A5 CH 564551A5 CH 1410574 A CH1410574 A CH 1410574A CH 1410574 A CH1410574 A CH 1410574A CH 564551 A5 CH564551 A5 CH 564551A5
- Authority
- CH
- Switzerland
- Prior art keywords
- triazine
- phthalimido
- ethylamino
- carbon atoms
- group
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 125000004414 alkyl thio group Chemical group 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 125000005544 phthalimido group Chemical group 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 5
- BAXKFBIHLQGUBU-UHFFFAOYSA-N 2-[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]isoindole-1,3-dione Chemical compound C(C)NC1=NC(=NC(=N1)N1C(C=2C(C1=O)=CC=CC2)=O)Cl BAXKFBIHLQGUBU-UHFFFAOYSA-N 0.000 description 4
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NNFFXPROGQRNAR-UHFFFAOYSA-N 2-[4-(1,3-dioxoisoindol-2-yl)-6-methoxy-1,3,5-triazin-2-yl]isoindole-1,3-dione Chemical compound C1(C=2C(C(N1C1=NC(=NC(=N1)N1C(C=3C(C1=O)=CC=CC3)=O)OC)=O)=CC=CC2)=O NNFFXPROGQRNAR-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KCZIUKYAJJEIQG-UHFFFAOYSA-N 1,3,5-triazin-2-amine Chemical class NC1=NC=NC=N1 KCZIUKYAJJEIQG-UHFFFAOYSA-N 0.000 description 1
- 150000000182 1,3,5-triazines Chemical class 0.000 description 1
- XUZGQOQQDLTZCP-UHFFFAOYSA-N 2-[4-(ethylamino)-6-methylsulfanyl-1,3,5-triazin-2-yl]isoindole-1,3-dione Chemical compound C(C)NC1=NC(=NC(=N1)N1C(C=2C(C1=O)=CC=CC2)=O)SC XUZGQOQQDLTZCP-UHFFFAOYSA-N 0.000 description 1
- ILGOUVXDTDKOAN-UHFFFAOYSA-N 2-[4-chloro-6-(1,3-dioxoisoindol-2-yl)-1,3,5-triazin-2-yl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1C1=NC(N2C(C3=CC=CC=C3C2=O)=O)=NC(Cl)=N1 ILGOUVXDTDKOAN-UHFFFAOYSA-N 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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- XHXXWWGGXFUMAJ-UHFFFAOYSA-N methanethiol;sodium Chemical compound [Na].SC XHXXWWGGXFUMAJ-UHFFFAOYSA-N 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- LNSAEWXPCBLGDX-UHFFFAOYSA-M sodium;2-(2,4-dichlorophenoxy)acetate;hydrate Chemical compound O.[Na+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl LNSAEWXPCBLGDX-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5344070A GB1324718A (en) | 1970-11-10 | 1970-11-10 | Phthalimido triazines |
| CH1410574A CH564551A5 (ja) | 1970-11-10 | 1970-11-12 | |
| CH1676070A CH557828A (de) | 1970-11-10 | 1970-11-12 | Verfahren zur herstellung substituierter phthalimido-1,3,5triazine. |
| CS74547A CS165316B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| CS74548A CS165317B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| SU1766767A SU437297A3 (ru) | 1970-11-10 | 1970-11-17 | Способ получения фталимидо-1,3,5-триазинов |
| SU1495559A SU429583A3 (ja) | 1970-11-10 | 1970-11-17 | |
| SU701495559D SU452962A3 (ru) | 1970-11-10 | 1970-11-17 | Способ получени фталимидо-1,3,5триазинов |
| NL7017108A NL7017108A (ja) | 1970-11-10 | 1970-11-23 | |
| FR7042588A FR2115622A5 (ja) | 1970-11-10 | 1970-11-26 | |
| BE759524D BE759524A (en) | 1970-11-10 | 1970-11-27 | Herbicidal phthalimido - 1,3,5-triazine derivs |
| US00098026A US3794641A (en) | 1970-11-10 | 1970-12-14 | Substituted phthalimido-1,3,5-triazines |
| CH1676070A CH583210A5 (ja) | 1970-11-10 | 1975-04-17 |
Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5344070 | 1970-11-10 | ||
| CH1676070A CH557828A (de) | 1970-11-10 | 1970-11-12 | Verfahren zur herstellung substituierter phthalimido-1,3,5triazine. |
| CH1410574A CH564551A5 (ja) | 1970-11-10 | 1970-11-12 | |
| CS74548A CS165317B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| CS74547A CS165316B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| SU1766767A SU437297A3 (ru) | 1970-11-10 | 1970-11-17 | Способ получения фталимидо-1,3,5-триазинов |
| SU1495559A SU429583A3 (ja) | 1970-11-10 | 1970-11-17 | |
| NL7017108A NL7017108A (ja) | 1970-11-10 | 1970-11-23 | |
| FR7042588A FR2115622A5 (ja) | 1970-11-10 | 1970-11-26 | |
| BE759524 | 1970-11-27 | ||
| US9802670A | 1970-12-14 | 1970-12-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH564551A5 true CH564551A5 (ja) | 1975-07-31 |
Family
ID=34109346
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1410574A CH564551A5 (ja) | 1970-11-10 | 1970-11-12 | |
| CH1676070A CH557828A (de) | 1970-11-10 | 1970-11-12 | Verfahren zur herstellung substituierter phthalimido-1,3,5triazine. |
| CH1676070A CH583210A5 (ja) | 1970-11-10 | 1975-04-17 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1676070A CH557828A (de) | 1970-11-10 | 1970-11-12 | Verfahren zur herstellung substituierter phthalimido-1,3,5triazine. |
| CH1676070A CH583210A5 (ja) | 1970-11-10 | 1975-04-17 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3794641A (ja) |
| BE (1) | BE759524A (ja) |
| CH (3) | CH564551A5 (ja) |
| CS (2) | CS165317B2 (ja) |
| FR (1) | FR2115622A5 (ja) |
| GB (1) | GB1324718A (ja) |
| NL (1) | NL7017108A (ja) |
| SU (3) | SU452962A3 (ja) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3896224A (en) * | 1972-04-10 | 1975-07-22 | Ciba Geigy Corp | 1-(4',6'-dichloro-s-triazin-2-ylcarbamoyl)-2-methoxy- carbonylamino-benzimidazole |
| KR19990087318A (ko) * | 1996-03-01 | 1999-12-27 | 마이클 제이. 켈리 | 사이클릭 이미도-1,3,5-트리아진 가교제 |
| JP4361273B2 (ja) * | 2001-02-27 | 2009-11-11 | アメリカ合衆国 | 潜在的な血管形成阻害剤としてのサリドマイド類似体 |
| AT410797B (de) * | 2001-07-26 | 2003-07-25 | Agrolinz Melamin Gmbh | Imidotriazinderivate |
| US8952895B2 (en) | 2011-06-03 | 2015-02-10 | Apple Inc. | Motion-based device operations |
| CN1867331B (zh) * | 2003-09-17 | 2010-05-26 | 美国政府健康及人类服务部 | 作为TNF-α调节剂的沙利度胺类似物 |
| WO2007120669A1 (en) * | 2006-04-13 | 2007-10-25 | The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Tetrahalogenated compounds useful as inhibitors of angiogenesis |
| WO2007137258A2 (en) * | 2006-05-22 | 2007-11-29 | New York University | C-glycolipids with enhanced th-1 profile |
| US8536170B2 (en) | 2011-06-24 | 2013-09-17 | E I Du Pont De Nemours And Company | Curable composition comprising a di-isoimide, method of curing, and the cured composition so formed |
| US8586734B2 (en) | 2011-06-24 | 2013-11-19 | E I Du Pont De Nemours And Company | Process for preparing substituted and unsubstituted diamino triazine aromatic di-isoimides |
| US8415470B2 (en) | 2011-06-24 | 2013-04-09 | E I Du Pont De Nemours And Company | Di-isoimide composition |
| US8927725B2 (en) | 2011-12-02 | 2015-01-06 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Thio compounds |
| CN105330650B (zh) * | 2015-11-04 | 2018-01-02 | 中北大学 | 一种非极性改性三聚氰胺基阻燃剂的制备方法及应用 |
| CN106866636B (zh) * | 2016-12-27 | 2019-09-03 | 中国石油天然气股份有限公司 | 一种亚酰胺类β晶型成核剂及其制备方法与应用 |
-
1970
- 1970-11-10 GB GB5344070A patent/GB1324718A/en not_active Expired
- 1970-11-12 CH CH1410574A patent/CH564551A5/de not_active IP Right Cessation
- 1970-11-12 CH CH1676070A patent/CH557828A/de not_active IP Right Cessation
- 1970-11-16 CS CS74548A patent/CS165317B2/cs unknown
- 1970-11-16 CS CS74547A patent/CS165316B2/cs unknown
- 1970-11-17 SU SU701495559D patent/SU452962A3/ru active
- 1970-11-17 SU SU1766767A patent/SU437297A3/ru active
- 1970-11-17 SU SU1495559A patent/SU429583A3/ru active
- 1970-11-23 NL NL7017108A patent/NL7017108A/xx unknown
- 1970-11-26 FR FR7042588A patent/FR2115622A5/fr not_active Expired
- 1970-11-27 BE BE759524D patent/BE759524A/xx unknown
- 1970-12-14 US US00098026A patent/US3794641A/en not_active Expired - Lifetime
-
1975
- 1975-04-17 CH CH1676070A patent/CH583210A5/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CH557828A (de) | 1975-01-15 |
| CH583210A5 (ja) | 1976-12-31 |
| SU452962A3 (ru) | 1974-12-05 |
| BE759524A (en) | 1971-04-30 |
| CS165317B2 (en) | 1975-12-22 |
| FR2115622A5 (ja) | 1972-07-07 |
| NL7017108A (ja) | 1972-05-25 |
| CS165316B2 (en) | 1975-12-22 |
| US3794641A (en) | 1974-02-26 |
| SU429583A3 (ja) | 1974-05-25 |
| GB1324718A (en) | 1973-07-25 |
| SU437297A3 (ru) | 1974-07-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |