CY1174A - Arylhydrazo-aldoximes and derivatives thereof exerting a fungicidal activity - Google Patents
Arylhydrazo-aldoximes and derivatives thereof exerting a fungicidal activity Download PDFInfo
- Publication number
- CY1174A CY1174A CY1174A CY117479A CY1174A CY 1174 A CY1174 A CY 1174A CY 1174 A CY1174 A CY 1174A CY 117479 A CY117479 A CY 117479A CY 1174 A CY1174 A CY 1174A
- Authority
- CY
- Cyprus
- Prior art keywords
- hydrazine
- oximinopropyl
- oximinoethyl
- hydrochloride
- dichlorophenyl
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 28
- 208000015181 infectious disease Diseases 0.000 claims description 20
- 230000003053 immunization Effects 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 241000233866 Fungi Species 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 244000045561 useful plants Species 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 9
- BIVUUOPIAYRCAP-UHFFFAOYSA-N aminoazanium;chloride Chemical compound Cl.NN BIVUUOPIAYRCAP-UHFFFAOYSA-N 0.000 claims 2
- 229940038531 phenylhydrazine hydrochloride Drugs 0.000 claims 2
- -1 3,4- dichlorophenyl - Chemical class 0.000 claims 1
- PZASBBILHPFPLH-UHFFFAOYSA-N aminoazanium;4-methylbenzenesulfonate Chemical compound NN.CC1=CC=C(S(O)(=O)=O)C=C1 PZASBBILHPFPLH-UHFFFAOYSA-N 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 32
- 150000001875 compounds Chemical class 0.000 description 25
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- 230000001143 conditioned effect Effects 0.000 description 15
- 230000000694 effects Effects 0.000 description 14
- 239000000243 solution Substances 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 8
- 238000011534 incubation Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 8
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 241000221577 Uromyces appendiculatus Species 0.000 description 5
- 239000007900 aqueous suspension Substances 0.000 description 5
- 239000012458 free base Substances 0.000 description 5
- 241000335053 Beta vulgaris Species 0.000 description 4
- 241000530549 Cercospora beticola Species 0.000 description 4
- 240000008067 Cucumis sativus Species 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 235000016068 Berberis vulgaris Nutrition 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 241000317981 Podosphaera fuliginea Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 241000972773 Aulopiformes Species 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241001157813 Cercospora Species 0.000 description 2
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000896238 Oidium Species 0.000 description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 2
- 241001281803 Plasmopara viticola Species 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 235000019515 salmon Nutrition 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 2
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 description 1
- SDYWXFYBZPNOFX-UHFFFAOYSA-N 3,4-dichloroaniline Chemical compound NC1=CC=C(Cl)C(Cl)=C1 SDYWXFYBZPNOFX-UHFFFAOYSA-N 0.000 description 1
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 1
- 101100391171 Schizosaccharomyces pombe (strain 972 / ATCC 24843) for3 gene Proteins 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 241000579741 Sphaerotheca <fungi> Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- PSLIMVZEAPALCD-UHFFFAOYSA-N ethanol;ethoxyethane Chemical compound CCO.CCOCC PSLIMVZEAPALCD-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- JCYWCSGERIELPG-UHFFFAOYSA-N imes Chemical class CC1=CC(C)=CC(C)=C1N1C=CN(C=2C(=CC(C)=CC=2C)C)[C]1 JCYWCSGERIELPG-UHFFFAOYSA-N 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000003407 synthetizing effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- A01N37/52—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 groups, e.g. carboxylic acid amidines
Landscapes
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT30322/78A IT1101444B (it) | 1978-11-29 | 1978-11-29 | Arilidrazo-aldossime e derivati ad attivita' fungicida |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1174A true CY1174A (en) | 1983-06-10 |
Family
ID=11229532
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY1174A CY1174A (en) | 1978-11-29 | 1979-11-28 | Arylhydrazo-aldoximes and derivatives thereof exerting a fungicidal activity |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4426393A (it) |
| JP (1) | JPS5592357A (it) |
| AR (1) | AR224380A1 (it) |
| AU (1) | AU534125B2 (it) |
| BR (1) | BR7907663A (it) |
| CH (1) | CH645512A5 (it) |
| CY (1) | CY1174A (it) |
| DE (1) | DE2947772A1 (it) |
| ES (1) | ES8107166A1 (it) |
| FR (1) | FR2442832B1 (it) |
| GB (2) | GB2080302B (it) |
| GR (1) | GR72726B (it) |
| IL (1) | IL58806A (it) |
| IT (1) | IT1101444B (it) |
| MA (1) | MA18650A1 (it) |
| PT (1) | PT70502A (it) |
| TR (1) | TR20480A (it) |
| ZA (1) | ZA796423B (it) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7592374B2 (en) * | 2005-03-03 | 2009-09-22 | Crompton Corporation | Insecticidal nitromethylene compounds |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2947782A (en) | 1957-12-23 | 1960-08-02 | Rohm & Haas | Aminoacetamidoximes |
| BE598730A (it) * | 1960-01-01 | |||
| FR2105698A5 (it) * | 1970-09-17 | 1972-04-28 | Roussel Uclaf | |
| DE2410184A1 (de) * | 1974-03-04 | 1975-10-02 | Bayer Ag | Chinonoxim-acylhydrazon-derivate, verfahren zu ihrer herstellung, sowie ihre verwendung als fungizide |
| DE2717437A1 (de) * | 1977-04-20 | 1978-10-26 | Hoechst Ag | Substituierte n-phenylformamidoxime und verfahren zu ihrer herstellung |
-
1978
- 1978-11-29 IT IT30322/78A patent/IT1101444B/it active
-
1979
- 1979-11-26 BR BR7907663A patent/BR7907663A/pt not_active IP Right Cessation
- 1979-11-26 JP JP15212679A patent/JPS5592357A/ja active Pending
- 1979-11-26 IL IL58806A patent/IL58806A/xx not_active IP Right Cessation
- 1979-11-26 MA MA18851A patent/MA18650A1/fr unknown
- 1979-11-27 AU AU53199/79A patent/AU534125B2/en not_active Ceased
- 1979-11-27 GR GR60619A patent/GR72726B/el unknown
- 1979-11-27 PT PT70502A patent/PT70502A/pt unknown
- 1979-11-27 ZA ZA00796423A patent/ZA796423B/xx unknown
- 1979-11-27 DE DE19792947772 patent/DE2947772A1/de not_active Withdrawn
- 1979-11-27 CH CH1054979A patent/CH645512A5/it not_active IP Right Cessation
- 1979-11-28 FR FR7929282A patent/FR2442832B1/fr not_active Expired
- 1979-11-28 GB GB8121903A patent/GB2080302B/en not_active Expired
- 1979-11-28 CY CY1174A patent/CY1174A/en unknown
- 1979-11-28 GB GB7940994A patent/GB2038634B/en not_active Expired
- 1979-11-28 ES ES486398A patent/ES8107166A1/es not_active Expired
- 1979-11-28 AR AR279052A patent/AR224380A1/es active
- 1979-11-29 TR TR20480A patent/TR20480A/xx unknown
-
1981
- 1981-09-29 US US06/306,730 patent/US4426393A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CH645512A5 (it) | 1984-10-15 |
| ES486398A0 (es) | 1980-12-16 |
| IT7830322A0 (it) | 1978-11-29 |
| JPS5592357A (en) | 1980-07-12 |
| MA18650A1 (fr) | 1980-07-01 |
| PT70502A (en) | 1979-12-01 |
| GB2080302A (en) | 1982-02-03 |
| IT1101444B (it) | 1985-09-28 |
| US4426393A (en) | 1984-01-17 |
| FR2442832B1 (fr) | 1985-09-06 |
| AU534125B2 (en) | 1984-01-05 |
| GB2080302B (en) | 1983-04-20 |
| ZA796423B (en) | 1980-11-26 |
| GR72726B (it) | 1983-12-01 |
| AR224380A1 (es) | 1981-11-30 |
| BR7907663A (pt) | 1980-09-09 |
| IL58806A (en) | 1983-12-30 |
| AU5319979A (en) | 1980-05-29 |
| IL58806A0 (en) | 1980-02-29 |
| DE2947772A1 (de) | 1980-06-12 |
| ES8107166A1 (es) | 1980-12-16 |
| GB2038634A (en) | 1980-07-30 |
| FR2442832A1 (fr) | 1980-06-27 |
| TR20480A (tr) | 1981-07-28 |
| GB2038634B (en) | 1982-08-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2515091C2 (de) | N-Acyl-N-phenyl-alaninderivate und -glycinderivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende fungizide Mittel | |
| DE2513732A1 (de) | Mikrobizide und wachstumsregulierende mittel | |
| JPS638302A (ja) | 殺生剤用効力増強剤 | |
| DE2513730A1 (de) | Halogenacetanilide als mikrobizide wirkstoffe | |
| EP0031054B1 (en) | Soil disinfectant composition, a method for preventing and controlling diseases in soil and certain phenylphosphinic acid salts | |
| DE2513789A1 (de) | Haloacylanilide als mikrobizide wirkstoffe | |
| DE2741437A1 (de) | Anilinderivate, verfahren zu ihrer herstellung und schaedlingsbekaempfungsmittel | |
| DE1946112A1 (de) | 1,1,1-Trichloraethan-Derivate | |
| DE2643403C2 (de) | Thiocarbonsäurederivate, Verfahren zu deren Herstellung und diese enthaltende Mittel | |
| CS235322B2 (en) | Fungicide and microbicidal agent and method of efficient component production | |
| CY1174A (en) | Arylhydrazo-aldoximes and derivatives thereof exerting a fungicidal activity | |
| US3641050A (en) | 1 5-substituted indazoles | |
| GB1041011A (en) | Fungicidal compositions and halogenated quinoxalines | |
| CS224622B2 (en) | Microbicide | |
| EP0113190A1 (en) | Alpha-hydroxy-beta-haloethylphosphinic acids and their salts, and their production and use | |
| PL107641B1 (pl) | Srodek szkodnikobojczy | |
| US3737543A (en) | Ectoparasiticidally active 2-arylamino-1-alkyl lactams | |
| US2413627A (en) | Parasiticidal compositions | |
| DE2643445A1 (de) | Mikrobizide mittel | |
| CH635313A5 (de) | Pflanzenmikrobizid wirkende hydrazino-acetanilid-derivate, verfahren zu ihrer herstellung sowie mikrobizide mittel mit diesen praeparaten als wirkstoffe. | |
| Dutton et al. | Insecticidal phosphoramidothio derivatives of the carbamate methomyl | |
| US4172713A (en) | Alkali and ammonium salts of zinc bis-N,N'(dithiocarboxy)-thiazolidin-4-carboxylic acid | |
| EP0179118B1 (en) | Herbicidal compositions with prolonged action and improved selectivity | |
| US3272699A (en) | Nu-(4-chlorophenylthiomethyl)-aniline fungicides | |
| CH617832A5 (en) | Novel microbicidal and plant-growth-regulating compositions containing oxalyl compounds. |