DD248952A5 - Agrochemische formulierung, insbesondere, nematozide, herbizide oder antifungale formulierung - Google Patents
Agrochemische formulierung, insbesondere, nematozide, herbizide oder antifungale formulierung Download PDFInfo
- Publication number
- DD248952A5 DD248952A5 DD86288740A DD28874086A DD248952A5 DD 248952 A5 DD248952 A5 DD 248952A5 DD 86288740 A DD86288740 A DD 86288740A DD 28874086 A DD28874086 A DD 28874086A DD 248952 A5 DD248952 A5 DD 248952A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- nitro
- groups
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- yield
- found
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- 239000000203 mixture Substances 0.000 title claims description 99
- 238000009472 formulation Methods 0.000 title claims description 65
- -1 ESPECIALLY Substances 0.000 title claims description 53
- 239000003905 agrochemical Substances 0.000 title claims description 10
- 230000001069 nematicidal effect Effects 0.000 title claims description 7
- 229940121375 antifungal agent Drugs 0.000 title claims description 6
- 230000000843 anti-fungal effect Effects 0.000 title claims description 5
- 239000005645 nematicide Substances 0.000 title description 3
- 239000004009 herbicide Substances 0.000 title 1
- 230000000749 insecticidal effect Effects 0.000 claims abstract description 10
- 239000004480 active ingredient Substances 0.000 claims description 34
- 239000000460 chlorine Chemical group 0.000 claims description 27
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 16
- 150000003863 ammonium salts Chemical class 0.000 claims description 13
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 13
- 239000013543 active substance Substances 0.000 claims description 12
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 230000002363 herbicidal effect Effects 0.000 claims description 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 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 claims description 6
- 229910052731 fluorine Chemical group 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
- 239000011737 fluorine Chemical group 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 125000001246 bromo group Chemical group Br* 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000002346 iodo group Chemical group I* 0.000 claims description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 3
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- 125000003107 substituted aryl group Chemical group 0.000 claims description 3
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
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- 239000011591 potassium Substances 0.000 claims description 2
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- ZAYAPAFPKFWESF-UHFFFAOYSA-N n-(4-cyano-2-nitrophenyl)-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane-1-carboxamide Chemical compound [O-][N+](=O)C1=CC(C#N)=CC=C1NC(=O)C1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C1(F)F ZAYAPAFPKFWESF-UHFFFAOYSA-N 0.000 description 1
- IVWACCSFRHDERF-UHFFFAOYSA-N n-(5-chloro-2-nitrophenyl)-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane-1-carboxamide Chemical compound [O-][N+](=O)C1=CC=C(Cl)C=C1NC(=O)C1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C1(F)F IVWACCSFRHDERF-UHFFFAOYSA-N 0.000 description 1
- KZALITGHBXEGQW-UHFFFAOYSA-N n-(5-ethoxy-2,4-dinitrophenyl)-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane-1-carboxamide Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(NC(=O)C2(F)C(C(F)(F)C(F)(F)C(F)(F)C2(F)F)(F)F)=C1[N+]([O-])=O KZALITGHBXEGQW-UHFFFAOYSA-N 0.000 description 1
- ZQQWGRXPKYAGPN-UHFFFAOYSA-N n-[3,5-bis(trifluoromethyl)phenyl]-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane-1-carboxamide Chemical compound FC(F)(F)C1=CC(C(F)(F)F)=CC(NC(=O)C2(F)C(C(F)(F)C(F)(F)C(F)(F)C2(F)F)(F)F)=C1 ZQQWGRXPKYAGPN-UHFFFAOYSA-N 0.000 description 1
- JUSLIJIQFCBPEK-UHFFFAOYSA-N n-[4-bromo-2-(trifluoromethyl)phenyl]-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane-1-carboxamide Chemical compound FC(F)(F)C1=CC(Br)=CC=C1NC(=O)C1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C1(F)F JUSLIJIQFCBPEK-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 150000004812 organic fluorine compounds Chemical class 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 1
- 125000005459 perfluorocyclohexyl group Chemical group 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000000375 suspending agent Substances 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
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- BGQMOFGZRJUORO-UHFFFAOYSA-M tetrapropylammonium bromide Chemical compound [Br-].CCC[N+](CCC)(CCC)CCC BGQMOFGZRJUORO-UHFFFAOYSA-M 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical class CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-O tributylazanium Chemical compound CCCC[NH+](CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-O 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A01N37/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides containing at least one oxygen or sulfur atom being directly attached to the same aromatic ring system
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72021285A | 1985-04-05 | 1985-04-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD248952A5 true DD248952A5 (de) | 1987-08-26 |
Family
ID=24893110
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD86288740A DD248952A5 (de) | 1985-04-05 | 1986-04-03 | Agrochemische formulierung, insbesondere, nematozide, herbizide oder antifungale formulierung |
Country Status (24)
| Country | Link |
|---|---|
| EP (1) | EP0201193B1 (fr) |
| JP (1) | JPS61236756A (fr) |
| KR (1) | KR900006517B1 (fr) |
| CN (1) | CN1012576B (fr) |
| AT (1) | ATE57681T1 (fr) |
| AU (1) | AU588296B2 (fr) |
| BR (1) | BR8601566A (fr) |
| CA (1) | CA1283918C (fr) |
| DD (1) | DD248952A5 (fr) |
| DE (1) | DE3675069D1 (fr) |
| DK (1) | DK154486A (fr) |
| ES (1) | ES8707922A1 (fr) |
| GR (1) | GR860894B (fr) |
| GT (1) | GT198600181A (fr) |
| HU (1) | HUT42750A (fr) |
| IL (1) | IL78393A (fr) |
| MY (1) | MY101438A (fr) |
| NZ (1) | NZ215672A (fr) |
| PH (1) | PH24477A (fr) |
| PL (2) | PL149800B1 (fr) |
| PT (1) | PT82322B (fr) |
| RO (1) | RO95059B (fr) |
| SU (1) | SU1561822A3 (fr) |
| ZA (1) | ZA862480B (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8607033D0 (en) * | 1986-03-21 | 1986-04-30 | Lilly Industries Ltd | Molluscicides |
| US5756000A (en) * | 1996-02-06 | 1998-05-26 | Minnesota Mining And Manufacturing Company | Perfluoro(alkoxycycloalkane)carbonyl fluoride compositions and their use |
| JP4601759B2 (ja) * | 2000-03-09 | 2010-12-22 | 石原薬品株式会社 | ペルフルオロデカリル基含有過酸化物及びその製造方法並びにペルフルオロデカリル基含有化合物の製造方法 |
| CN104447433A (zh) * | 2014-11-11 | 2015-03-25 | 常州大学 | 一种合成3,5-二溴对甲苯磺酰氯的方法 |
| CN119080657B (zh) * | 2024-11-06 | 2025-01-28 | 湖南工程学院 | 一种快速合成硫氰基取代的甲酰苯胺的制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3211987A1 (de) * | 1981-04-03 | 1982-10-21 | CIBA-GEIGY AG, 4002 Basel | Cyclobutandicarbonsaeurederivate, verfahren zu deren herstellung und deren verwendung als fungizid |
-
1986
- 1986-03-31 IL IL78393A patent/IL78393A/xx unknown
- 1986-04-01 AU AU55525/86A patent/AU588296B2/en not_active Ceased
- 1986-04-02 NZ NZ215672A patent/NZ215672A/xx unknown
- 1986-04-02 AT AT86302434T patent/ATE57681T1/de active
- 1986-04-02 EP EP86302434A patent/EP0201193B1/fr not_active Expired - Lifetime
- 1986-04-02 PH PH33614A patent/PH24477A/en unknown
- 1986-04-02 DE DE8686302434T patent/DE3675069D1/de not_active Expired - Lifetime
- 1986-04-02 PT PT82322A patent/PT82322B/pt not_active IP Right Cessation
- 1986-04-02 RO RO122858A patent/RO95059B/ro unknown
- 1986-04-03 CA CA000505802A patent/CA1283918C/fr not_active Expired - Lifetime
- 1986-04-03 CN CN86102271A patent/CN1012576B/zh not_active Expired
- 1986-04-03 HU HU861425A patent/HUT42750A/hu unknown
- 1986-04-03 ZA ZA862480A patent/ZA862480B/xx unknown
- 1986-04-03 DD DD86288740A patent/DD248952A5/de not_active IP Right Cessation
- 1986-04-03 ES ES553704A patent/ES8707922A1/es not_active Expired
- 1986-04-03 GR GR860894A patent/GR860894B/el unknown
- 1986-04-04 KR KR1019860002564A patent/KR900006517B1/ko not_active Expired
- 1986-04-04 SU SU864027246A patent/SU1561822A3/ru active
- 1986-04-04 PL PL1986267525A patent/PL149800B1/pl unknown
- 1986-04-04 DK DK154486A patent/DK154486A/da not_active Application Discontinuation
- 1986-04-04 JP JP61079064A patent/JPS61236756A/ja active Pending
- 1986-04-04 GT GT198600181A patent/GT198600181A/es unknown
- 1986-04-04 PL PL1986258779A patent/PL149721B1/pl unknown
- 1986-04-04 BR BR8601566A patent/BR8601566A/pt unknown
-
1987
- 1987-09-23 MY MYPI87001894A patent/MY101438A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUT42750A (en) | 1987-08-28 |
| CN86102271A (zh) | 1986-12-03 |
| CN1012576B (zh) | 1991-05-08 |
| BR8601566A (pt) | 1986-12-09 |
| EP0201193B1 (fr) | 1990-10-24 |
| IL78393A (en) | 1990-12-23 |
| AU5552586A (en) | 1986-10-09 |
| EP0201193A3 (en) | 1988-05-18 |
| PL149800B1 (en) | 1990-03-31 |
| AU588296B2 (en) | 1989-09-14 |
| PH24477A (en) | 1990-07-18 |
| PL149721B1 (en) | 1990-03-31 |
| RO95059B (ro) | 1988-08-17 |
| ATE57681T1 (de) | 1990-11-15 |
| PL267525A1 (en) | 1988-03-03 |
| KR900006517B1 (ko) | 1990-09-03 |
| NZ215672A (en) | 1990-11-27 |
| DK154486A (da) | 1986-10-06 |
| DK154486D0 (da) | 1986-04-04 |
| JPS61236756A (ja) | 1986-10-22 |
| GR860894B (en) | 1986-07-29 |
| PT82322A (en) | 1986-05-01 |
| ZA862480B (en) | 1987-02-25 |
| ES553704A0 (es) | 1987-09-01 |
| DE3675069D1 (de) | 1990-11-29 |
| CA1283918C (fr) | 1991-05-07 |
| PT82322B (pt) | 1988-10-14 |
| IL78393A0 (en) | 1986-07-31 |
| ES8707922A1 (es) | 1987-09-01 |
| RO95059A (fr) | 1988-08-15 |
| EP0201193A2 (fr) | 1986-11-12 |
| GT198600181A (es) | 1987-09-26 |
| MY101438A (en) | 1991-11-18 |
| SU1561822A3 (ru) | 1990-04-30 |
| KR860007874A (ko) | 1986-11-10 |
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