HU176915B - Fungicidnye kompozicii soderzhahhie zamehhennye fenoksi-triazolil-butil-slozhnykh efirov,i sposob poluchenija aktivnykh agentov - Google Patents
Fungicidnye kompozicii soderzhahhie zamehhennye fenoksi-triazolil-butil-slozhnykh efirov,i sposob poluchenija aktivnykh agentov Download PDFInfo
- Publication number
- HU176915B HU176915B HU77BA3494A HUBA003494A HU176915B HU 176915 B HU176915 B HU 176915B HU 77BA3494 A HU77BA3494 A HU 77BA3494A HU BA003494 A HUBA003494 A HU BA003494A HU 176915 B HU176915 B HU 176915B
- Authority
- HU
- Hungary
- Prior art keywords
- formula
- triazolyl
- solvent
- active ingredient
- optionally
- Prior art date
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- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 8
- 238000000034 method Methods 0.000 title claims description 36
- 239000013543 active substance Substances 0.000 title description 6
- 239000000417 fungicide Substances 0.000 title description 2
- 239000004480 active ingredient Substances 0.000 claims abstract description 81
- 239000000203 mixture Substances 0.000 claims abstract description 44
- 150000001875 compounds Chemical class 0.000 claims abstract description 39
- 239000002904 solvent Substances 0.000 claims abstract description 33
- -1 substituted-phenyl Chemical group 0.000 claims abstract description 33
- 150000003839 salts Chemical class 0.000 claims abstract description 20
- 229910052751 metal Chemical class 0.000 claims abstract description 13
- 239000002184 metal Chemical class 0.000 claims abstract description 13
- 239000003054 catalyst Substances 0.000 claims abstract description 10
- 239000002253 acid Substances 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 6
- 239000003085 diluting agent Substances 0.000 claims abstract description 5
- 150000004820 halides Chemical class 0.000 claims abstract description 5
- 239000007788 liquid Substances 0.000 claims abstract description 5
- 239000007787 solid Substances 0.000 claims abstract description 5
- 150000004696 coordination complex Chemical class 0.000 claims abstract description 4
- 239000012948 isocyanate Substances 0.000 claims abstract description 4
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 4
- 239000004094 surface-active agent Substances 0.000 claims abstract description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 21
- 238000002360 preparation method Methods 0.000 claims description 19
- 239000003995 emulsifying agent Substances 0.000 claims description 11
- 235000013312 flour Nutrition 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000002270 dispersing agent Substances 0.000 claims description 5
- 150000002367 halogens Chemical group 0.000 claims description 5
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 claims description 4
- 239000000969 carrier Substances 0.000 claims description 4
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000001401 1,2,4-triazol-4-yl group Chemical group N=1N=C([H])N([*])C=1[H] 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims description 2
- 239000002969 artificial stone Substances 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000000068 chlorophenyl group Chemical group 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001425 triazolyl group Chemical group 0.000 claims description 2
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 239000003495 polar organic solvent Substances 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract description 8
- 150000008065 acid anhydrides Chemical class 0.000 abstract description 6
- 239000003795 chemical substances by application Substances 0.000 abstract description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 3
- 125000003282 alkyl amino group Chemical group 0.000 abstract description 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 2
- 239000012458 free base Substances 0.000 abstract description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 2
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004970 halomethyl group Chemical group 0.000 abstract 1
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- 238000006243 chemical reaction Methods 0.000 description 11
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 241000221785 Erysiphales Species 0.000 description 4
- 240000005979 Hordeum vulgare Species 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
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- 238000001953 recrystallisation Methods 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- 206010017533 Fungal infection Diseases 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
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- YJUFFIJJZPSEEE-UHFFFAOYSA-N 1-phenoxy-1-(2H-triazol-4-yl)butan-1-ol Chemical class O(C1=CC=CC=C1)C(CCC)(O)C=1N=NNC1 YJUFFIJJZPSEEE-UHFFFAOYSA-N 0.000 description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762600799 DE2600799A1 (de) | 1976-01-10 | 1976-01-10 | Acylierte triazolyl-0,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU176915B true HU176915B (hu) | 1981-06-28 |
Family
ID=5967270
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU77BA3494A HU176915B (hu) | 1976-01-10 | 1977-01-06 | Fungicidnye kompozicii soderzhahhie zamehhennye fenoksi-triazolil-butil-slozhnykh efirov,i sposob poluchenija aktivnykh agentov |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US4145428A (en, 2012) |
| JP (1) | JPS5287170A (en, 2012) |
| AT (1) | AT351863B (en, 2012) |
| AU (1) | AU502450B2 (en, 2012) |
| BE (1) | BE850239A (en, 2012) |
| BR (1) | BR7700076A (en, 2012) |
| CA (1) | CA1077943A (en, 2012) |
| CH (1) | CH629078A5 (en, 2012) |
| CS (1) | CS195322B2 (en, 2012) |
| DD (1) | DD129395A5 (en, 2012) |
| DE (1) | DE2600799A1 (en, 2012) |
| DK (1) | DK5877A (en, 2012) |
| EG (1) | EG12330A (en, 2012) |
| FI (1) | FI61699C (en, 2012) |
| FR (1) | FR2337719A1 (en, 2012) |
| GB (1) | GB1505241A (en, 2012) |
| GR (1) | GR62062B (en, 2012) |
| HU (1) | HU176915B (en, 2012) |
| IL (1) | IL51230A (en, 2012) |
| IT (1) | IT1077110B (en, 2012) |
| NL (1) | NL7700143A (en, 2012) |
| NZ (1) | NZ183028A (en, 2012) |
| PH (1) | PH14133A (en, 2012) |
| PL (1) | PL101196B1 (en, 2012) |
| PT (1) | PT66046B (en, 2012) |
| SE (1) | SE7700065L (en, 2012) |
| SU (1) | SU621302A3 (en, 2012) |
| TR (1) | TR18945A (en, 2012) |
| ZA (1) | ZA77101B (en, 2012) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2758784A1 (de) * | 1977-12-29 | 1979-07-12 | Basf Ag | Triazolyl-glykolaether |
| DE2800544A1 (de) | 1978-01-07 | 1979-07-19 | Bayer Ag | Carbamoyl-triazolyl-o,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE2811919A1 (de) * | 1978-03-18 | 1979-09-27 | Bayer Ag | Acylierte 1-azolyl-2-hydroxy-butan- derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE2827968A1 (de) * | 1978-06-26 | 1980-01-10 | Bayer Ag | Sulfenylierte carbamoyl-triazolyl- o,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE2926280A1 (de) * | 1979-06-29 | 1981-01-08 | Basf Ag | Fungizide alpha -triazolylglykolderivate, ihre herstellung und verwendung |
| DE2931756A1 (de) * | 1979-08-04 | 1981-02-19 | Bayer Ag | Antimikrobielle mittel |
| DE2931755A1 (de) * | 1979-08-04 | 1981-02-19 | Bayer Ag | 1,2,4-triazolyl-enolether, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE3019049A1 (de) * | 1980-05-19 | 1981-12-03 | Basf Ag, 6700 Ludwigshafen | Neue azolverbindungen |
| DE3132335A1 (de) * | 1981-08-17 | 1983-03-03 | Bayer Ag, 5090 Leverkusen | Substituierte azolyl-phenoxy-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE3313719A1 (de) * | 1983-04-15 | 1984-10-18 | Bayer Ag, 5090 Leverkusen | Phosphorylierte azolyl-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
| DE3315262A1 (de) * | 1983-04-27 | 1984-10-31 | Bayer Ag, 5090 Leverkusen | Carbamoylierte azolylalkyl-phenoxy-carbinole, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenschutzmittel |
| JPS63178120U (en, 2012) * | 1987-03-26 | 1988-11-17 | ||
| US5113036A (en) * | 1990-04-25 | 1992-05-12 | At&T Bell Laboratories | Modular cable |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH500663A (de) * | 1968-05-02 | 1970-12-31 | Ciba Geigy Ag | Verwendung von Diphenylketonen zur Bekämpfung schädlicher Mikroorganismen ausserhalb der Textilindustrie |
| DE2324010C3 (de) * | 1973-05-12 | 1981-10-08 | Bayer Ag, 5090 Leverkusen | 1-Substituierte 2-Triazolyl-2-phenoxyäthanol-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Pilzen |
| DE2604761A1 (de) * | 1976-02-07 | 1977-08-11 | Bayer Ag | Acylierte imidazolyl-o,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
-
1976
- 1976-01-10 DE DE19762600799 patent/DE2600799A1/de not_active Withdrawn
- 1976-12-21 US US05/753,651 patent/US4145428A/en not_active Expired - Lifetime
- 1976-12-29 SU SU762435052A patent/SU621302A3/ru active
-
1977
- 1977-01-04 PH PH19315A patent/PH14133A/en unknown
- 1977-01-04 SE SE7700065A patent/SE7700065L/xx not_active Application Discontinuation
- 1977-01-06 CH CH14577A patent/CH629078A5/de not_active IP Right Cessation
- 1977-01-06 AU AU21094/77A patent/AU502450B2/en not_active Expired
- 1977-01-06 HU HU77BA3494A patent/HU176915B/hu unknown
- 1977-01-07 DK DK5877A patent/DK5877A/da not_active Application Discontinuation
- 1977-01-07 DD DD7700196862A patent/DD129395A5/xx unknown
- 1977-01-07 FI FI770045A patent/FI61699C/fi not_active IP Right Cessation
- 1977-01-07 IL IL51230A patent/IL51230A/xx unknown
- 1977-01-07 ZA ZA770101A patent/ZA77101B/xx unknown
- 1977-01-07 BR BR7700076A patent/BR7700076A/pt unknown
- 1977-01-07 PL PL1977195196A patent/PL101196B1/pl unknown
- 1977-01-07 IT IT19119/77A patent/IT1077110B/it active
- 1977-01-07 TR TR18945A patent/TR18945A/xx unknown
- 1977-01-07 GB GB547/77A patent/GB1505241A/en not_active Expired
- 1977-01-07 CA CA269,296A patent/CA1077943A/en not_active Expired
- 1977-01-07 CS CS77119A patent/CS195322B2/cs unknown
- 1977-01-07 NL NL7700143A patent/NL7700143A/xx not_active Application Discontinuation
- 1977-01-07 NZ NZ183028A patent/NZ183028A/xx unknown
- 1977-01-07 PT PT66046A patent/PT66046B/pt unknown
- 1977-01-08 GR GR52537A patent/GR62062B/el unknown
- 1977-01-10 FR FR7700510A patent/FR2337719A1/fr active Granted
- 1977-01-10 BE BE173963A patent/BE850239A/xx not_active IP Right Cessation
- 1977-01-10 EG EG17/77A patent/EG12330A/xx active
- 1977-01-10 AT AT7877A patent/AT351863B/de not_active IP Right Cessation
- 1977-01-10 JP JP88577A patent/JPS5287170A/ja active Granted
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