UA71998C2 - Fungicides - Google Patents
Fungicides Download PDFInfo
- Publication number
- UA71998C2 UA71998C2 UA2002043068A UA2002043068A UA71998C2 UA 71998 C2 UA71998 C2 UA 71998C2 UA 2002043068 A UA2002043068 A UA 2002043068A UA 2002043068 A UA2002043068 A UA 2002043068A UA 71998 C2 UA71998 C2 UA 71998C2
- Authority
- UA
- Ukraine
- Prior art keywords
- compound
- formula
- propyl
- compounds
- plant
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 238000012876 topography Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 9
- 241000233866 Fungi Species 0.000 abstract description 5
- 238000000034 method Methods 0.000 abstract description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000004254 Ammonium phosphate Substances 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 2
- 235000019289 ammonium phosphates Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- -1 co 30 ofureis Chemical compound 0.000 description 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000009331 sowing Methods 0.000 description 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 description 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 description 1
- 239000005730 Azoxystrobin Substances 0.000 description 1
- 239000005734 Benalaxyl Substances 0.000 description 1
- 239000005747 Chlorothalonil Substances 0.000 description 1
- SZJGCIDQIHIMMG-UHFFFAOYSA-N Cl.CCCOC(N)=O Chemical compound Cl.CCCOC(N)=O SZJGCIDQIHIMMG-UHFFFAOYSA-N 0.000 description 1
- 239000005756 Cymoxanil Substances 0.000 description 1
- 239000005758 Cyprodinil Substances 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- 239000005772 Famoxadone Substances 0.000 description 1
- 239000005789 Folpet Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 239000005867 Iprodione Substances 0.000 description 1
- 239000005800 Kresoxim-methyl Substances 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 239000005802 Mancozeb Substances 0.000 description 1
- 239000005807 Metalaxyl Substances 0.000 description 1
- 241000233614 Phytophthora Species 0.000 description 1
- MKIMSXGUTQTKJU-UHFFFAOYSA-N Propamocarb hydrochloride Chemical compound [Cl-].CCCOC(=O)NCCC[NH+](C)C MKIMSXGUTQTKJU-UHFFFAOYSA-N 0.000 description 1
- 239000005828 Pyrimethanil Substances 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 239000005837 Spiroxamine Substances 0.000 description 1
- 229930182692 Strobilurin Natural products 0.000 description 1
- 239000005857 Trifloxystrobin Substances 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 description 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 1
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-O propan-1-aminium Chemical compound CCC[NH3+] WGYKZJWCGVVSQN-UHFFFAOYSA-O 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- ASTWEMOBIXQPPV-UHFFFAOYSA-K trisodium;phosphate;dodecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[Na+].[O-]P([O-])([O-])=O ASTWEMOBIXQPPV-UHFFFAOYSA-K 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/20—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9921930.5A GB9921930D0 (en) | 1999-09-17 | 1999-09-17 | Fugicides |
| PCT/EP2000/009360 WO2001021626A1 (en) | 1999-09-17 | 2000-09-15 | Fungicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA71998C2 true UA71998C2 (en) | 2005-01-17 |
Family
ID=10861047
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2002043068A UA71998C2 (en) | 1999-09-17 | 2000-09-15 | Fungicides |
Country Status (32)
| Country | Link |
|---|---|
| US (1) | US6639097B1 (de) |
| EP (1) | EP1212332B1 (de) |
| JP (1) | JP2003509514A (de) |
| KR (1) | KR100695637B1 (de) |
| CN (1) | CN1374964A (de) |
| AR (1) | AR029003A1 (de) |
| AT (1) | ATE259367T1 (de) |
| AU (1) | AU780952B2 (de) |
| BG (1) | BG65136B1 (de) |
| BR (1) | BR0014571B1 (de) |
| CA (1) | CA2384027C (de) |
| CO (1) | CO5221061A1 (de) |
| CZ (1) | CZ298930B6 (de) |
| DE (1) | DE60008253T2 (de) |
| DK (1) | DK1212332T3 (de) |
| EA (1) | EA200200373A1 (de) |
| ES (1) | ES2214323T3 (de) |
| GB (1) | GB9921930D0 (de) |
| HK (1) | HK1048124A1 (de) |
| HR (1) | HRP20020337B1 (de) |
| HU (1) | HUP0202777A3 (de) |
| IL (1) | IL148574A (de) |
| MA (1) | MA25502A1 (de) |
| MX (1) | MXPA02002850A (de) |
| NZ (1) | NZ517707A (de) |
| PL (1) | PL192383B1 (de) |
| PT (1) | PT1212332E (de) |
| SK (1) | SK285651B6 (de) |
| TW (1) | TW587919B (de) |
| UA (1) | UA71998C2 (de) |
| WO (1) | WO2001021626A1 (de) |
| ZA (1) | ZA200202082B (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101268974B1 (ko) * | 2005-10-19 | 2013-05-29 | 바이엘 크롭사이언스 인코포레이티드 | 곰팡이의 살진균 구제 |
| EP3532630B1 (de) | 2016-10-31 | 2020-06-24 | Eastman Chemical Company | Enzymatische zubereitung von propamocarb |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3047962B2 (ja) * | 1996-08-22 | 2000-06-05 | 日華化学株式会社 | 殺菌消毒剤 |
| FR2761577B1 (fr) * | 1997-04-04 | 1999-05-14 | Rhone Poulenc Agrochimie | Composition fongicide synergique a base de propacarbe et de derives de l'acide phosphoreux |
| DE69904444T2 (de) * | 1998-02-20 | 2003-07-10 | Aventis Cropscience Uk Ltd | Fungizide |
-
1999
- 1999-09-17 GB GBGB9921930.5A patent/GB9921930D0/en not_active Ceased
-
2000
- 2000-09-14 CO CO00069736A patent/CO5221061A1/es not_active Application Discontinuation
- 2000-09-15 SK SK385-2002A patent/SK285651B6/sk not_active IP Right Cessation
- 2000-09-15 KR KR1020027003499A patent/KR100695637B1/ko not_active IP Right Cessation
- 2000-09-15 BR BRPI0014571-8A patent/BR0014571B1/pt not_active IP Right Cessation
- 2000-09-15 CN CN00813041A patent/CN1374964A/zh active Pending
- 2000-09-15 MX MXPA02002850A patent/MXPA02002850A/es active IP Right Grant
- 2000-09-15 NZ NZ517707A patent/NZ517707A/en unknown
- 2000-09-15 AR ARP000104860A patent/AR029003A1/es active IP Right Grant
- 2000-09-15 JP JP2001525001A patent/JP2003509514A/ja active Pending
- 2000-09-15 US US10/088,379 patent/US6639097B1/en not_active Expired - Lifetime
- 2000-09-15 UA UA2002043068A patent/UA71998C2/uk unknown
- 2000-09-15 WO PCT/EP2000/009360 patent/WO2001021626A1/en active IP Right Grant
- 2000-09-15 EP EP00966073A patent/EP1212332B1/de not_active Expired - Lifetime
- 2000-09-15 IL IL14857400A patent/IL148574A/xx unknown
- 2000-09-15 AU AU76595/00A patent/AU780952B2/en not_active Ceased
- 2000-09-15 PL PL353924A patent/PL192383B1/pl not_active IP Right Cessation
- 2000-09-15 CZ CZ20020941A patent/CZ298930B6/cs not_active IP Right Cessation
- 2000-09-15 HU HU0202777A patent/HUP0202777A3/hu unknown
- 2000-09-15 ES ES00966073T patent/ES2214323T3/es not_active Expired - Lifetime
- 2000-09-15 CA CA002384027A patent/CA2384027C/en not_active Expired - Fee Related
- 2000-09-15 DK DK00966073T patent/DK1212332T3/da active
- 2000-09-15 PT PT00966073T patent/PT1212332E/pt unknown
- 2000-09-15 EA EA200200373A patent/EA200200373A1/ru unknown
- 2000-09-15 DE DE60008253T patent/DE60008253T2/de not_active Expired - Lifetime
- 2000-09-15 AT AT00966073T patent/ATE259367T1/de active
- 2000-10-16 TW TW089121586A patent/TW587919B/zh not_active IP Right Cessation
-
2002
- 2002-03-11 BG BG106505A patent/BG65136B1/bg unknown
- 2002-03-13 ZA ZA200202082A patent/ZA200202082B/en unknown
- 2002-04-10 MA MA26593A patent/MA25502A1/fr unknown
- 2002-04-16 HR HR20020337A patent/HRP20020337B1/xx not_active IP Right Cessation
-
2003
- 2003-01-16 HK HK03100401.0A patent/HK1048124A1/zh unknown
Also Published As
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