DE1120800B - Verwendung von N substituierten Sydnonen als Mittel zur Forderung des Pflanzenwachstums und zur Vernichtung von Pilzen auf Pflanzen - Google Patents
Verwendung von N substituierten Sydnonen als Mittel zur Forderung des Pflanzenwachstums und zur Vernichtung von Pilzen auf PflanzenInfo
- Publication number
- DE1120800B DE1120800B DENDAT1120800D DE1120800DA DE1120800B DE 1120800 B DE1120800 B DE 1120800B DE NDAT1120800 D DENDAT1120800 D DE NDAT1120800D DE 1120800D A DE1120800D A DE 1120800DA DE 1120800 B DE1120800 B DE 1120800B
- Authority
- DE
- Germany
- Prior art keywords
- plants
- sydnones
- phenyl
- substituted
- substituent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 230000008635 plant growth Effects 0.000 title claims description 6
- 241000233866 Fungi Species 0.000 title claims description 4
- 230000001737 promoting effect Effects 0.000 title claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- -1 aromatic halogen Chemical class 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 37
- 239000000126 substance Substances 0.000 description 18
- 230000006378 damage Effects 0.000 description 10
- 239000000417 fungicide Substances 0.000 description 8
- 201000010099 disease Diseases 0.000 description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 7
- 230000012010 growth Effects 0.000 description 7
- KQEVEDHJIGSXDK-UHFFFAOYSA-N 3-phenyloxadiazol-3-ium-5-olate Chemical compound O1C([O-])=C[N+](C=2C=CC=CC=2)=N1 KQEVEDHJIGSXDK-UHFFFAOYSA-N 0.000 description 5
- 230000000855 fungicidal effect Effects 0.000 description 5
- BPBGWPOHEYHTJC-UHFFFAOYSA-O 3-(2-methylphenyl)-2h-oxadiazol-3-ium-5-one Chemical compound CC1=CC=CC=C1[N+]1=CC(=O)ON1 BPBGWPOHEYHTJC-UHFFFAOYSA-O 0.000 description 4
- PESUOZMEAOPWMA-UHFFFAOYSA-N 3-(3-chlorophenyl)oxadiazol-3-ium-5-olate Chemical compound O1C([O-])=C[N+](C=2C=C(Cl)C=CC=2)=N1 PESUOZMEAOPWMA-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ILLZWHORGXIGRG-UHFFFAOYSA-N 3-(3-methylphenyl)oxadiazol-3-ium-5-olate Chemical compound CC1=CC=CC([N+]2=NOC([O-])=C2)=C1 ILLZWHORGXIGRG-UHFFFAOYSA-N 0.000 description 3
- VUXSBVYENPHXGE-UHFFFAOYSA-N 3-(4-chlorophenyl)oxadiazol-3-ium-5-olate Chemical compound O1C([O-])=C[N+](C=2C=CC(Cl)=CC=2)=N1 VUXSBVYENPHXGE-UHFFFAOYSA-N 0.000 description 3
- 241000221577 Uromyces appendiculatus Species 0.000 description 3
- NVRSPIKUPKOSIY-UHFFFAOYSA-N chembl1743348 Chemical group CC=1N=NOC=1O NVRSPIKUPKOSIY-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 230000009897 systematic effect Effects 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- XIIZHMNSBLVHKS-UHFFFAOYSA-N 3-(4-methylphenyl)oxadiazol-3-ium-5-olate Chemical compound C1=CC(C)=CC=C1[N+]1=NOC([O-])=C1 XIIZHMNSBLVHKS-UHFFFAOYSA-N 0.000 description 2
- GUBQLELJVCXLMV-UHFFFAOYSA-N 3-benzyloxadiazol-3-ium-5-olate Chemical compound O1C([O-])=C[N+](CC=2C=CC=CC=2)=N1 GUBQLELJVCXLMV-UHFFFAOYSA-N 0.000 description 2
- YJSBCTYMQCSFQM-UHFFFAOYSA-N 3-butyloxadiazol-3-ium-5-olate Chemical compound CCCC[N+]=1C=C([O-])ON=1 YJSBCTYMQCSFQM-UHFFFAOYSA-N 0.000 description 2
- LBWGAPRXZZUQPR-UHFFFAOYSA-N 3-cyclohexyloxadiazol-3-ium-5-olate Chemical compound O1C([O-])=C[N+](C2CCCCC2)=N1 LBWGAPRXZZUQPR-UHFFFAOYSA-N 0.000 description 2
- ZKDMASAOLMIRQV-UHFFFAOYSA-N 3-naphthalen-2-yloxadiazol-3-ium-5-olate Chemical compound O1C([O-])=C[N+](C=2C=C3C=CC=CC3=CC=2)=N1 ZKDMASAOLMIRQV-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000227653 Lycopersicon Species 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 206010037888 Rash pustular Diseases 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 208000029561 pustule Diseases 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- MDXSZGJOBTZROY-UHFFFAOYSA-N 3-(4-methoxyphenyl)oxadiazol-3-ium-5-olate Chemical compound C1=CC(OC)=CC=C1[N+]1=NOC([O-])=C1 MDXSZGJOBTZROY-UHFFFAOYSA-N 0.000 description 1
- RKAKVBXADCSTLE-UHFFFAOYSA-N 3-(4-nitrophenyl)oxadiazol-3-ium-5-olate Chemical compound O1C([O-])=C[N+](C=2C=CC(=CC=2)[N+]([O-])=O)=N1 RKAKVBXADCSTLE-UHFFFAOYSA-N 0.000 description 1
- GUBQLELJVCXLMV-UHFFFAOYSA-O 3-benzyl-2h-oxadiazol-3-ium-5-one Chemical compound N1OC(=O)C=[N+]1CC1=CC=CC=C1 GUBQLELJVCXLMV-UHFFFAOYSA-O 0.000 description 1
- KUYNWZKDWRYCIH-UHFFFAOYSA-N 3-methyloxadiazol-3-ium-5-olate Chemical compound C[N+]=1C=C([O-])ON=1 KUYNWZKDWRYCIH-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 241000213004 Alternaria solani Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/04—1,2,3-Oxadiazoles; Hydrogenated 1,2,3-oxadiazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US890191XA | 1959-05-14 | 1959-05-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1120800B true DE1120800B (de) | 1961-12-28 |
Family
ID=22214981
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT1120800D Pending DE1120800B (de) | 1959-05-14 | Verwendung von N substituierten Sydnonen als Mittel zur Forderung des Pflanzenwachstums und zur Vernichtung von Pilzen auf Pflanzen |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE590620A (enrdf_load_stackoverflow) |
DE (1) | DE1120800B (enrdf_load_stackoverflow) |
GB (1) | GB890191A (enrdf_load_stackoverflow) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5064617A (en) * | 1990-02-16 | 1991-11-12 | Leco Corporation | Combustion system |
CN111057024B (zh) * | 2019-12-24 | 2025-02-07 | 华东理工大学 | 悉尼酮与悉尼酮亚胺类化合物及其制备方法和用途 |
-
0
- DE DENDAT1120800D patent/DE1120800B/de active Pending
- BE BE590620D patent/BE590620A/xx unknown
-
1960
- 1960-04-27 GB GB14692/60A patent/GB890191A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB890191A (en) | 1962-02-28 |
BE590620A (enrdf_load_stackoverflow) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1108975B (de) | Fungicide Mittel auf der Basis von Anilinverbindungen | |
DE1913726B2 (de) | Mittel zur Bekämpfung von Pilzen auf Basis von Pyrazinderivaten | |
DE1120800B (de) | Verwendung von N substituierten Sydnonen als Mittel zur Forderung des Pflanzenwachstums und zur Vernichtung von Pilzen auf Pflanzen | |
DE2440787A1 (de) | Verfahren zur selektiven bekaempfung von unkraut in kentucky-blaugras | |
DE893590C (de) | Antiparasitische Mittel zur Behandlung von im Wachstum befindlichen Pflanzen | |
DE1025203B (de) | Bekaempfung von Pflanzenparasiten | |
DE1143668B (de) | Fungizide Mittel | |
DE1567153C3 (de) | Neue N-Carbamoyloxydicarbonsäureimide | |
DE1110942B (de) | Systemisch wirkendes Mittel, insbesondere gegen Pilzbefall von Pflanzen | |
DE1017405B (de) | Fungizide Pflanzenschutzmittel mit innertherapeutischer Wirksamkeit | |
CH233721A (de) | Verfahren zur Vergrämung pflanzenschädigender Dipteren. | |
DE2659508A1 (de) | Unkrautbekaempfung in lauchkulturen | |
DE2246403A1 (de) | Dihalogenhydroxybenzolsulfonamidderivate und ihre herstellung und anwendung | |
DE1160235B (de) | Fungizide Mittel | |
Thomas et al. | Investigations into the control of carrot fly on celery. | |
AT240645B (de) | Mittel zur Bodenbehandlung zum Schutz von Weinstöcken gegen Rebläuse | |
US3301750A (en) | Bis (substituted amino) nu alkyl diphenylamines as fungicides and algaecides | |
AT251969B (de) | Fungizide Zusammensetzung mit Aktivität gegen Oidium | |
AT246492B (de) | Schädlingsbekämpfungsmittel | |
DE975426C (de) | Vernichtung der Eier von Milben und Spinnenmilben | |
DE948101C (de) | Bekaempfung pilzlicher Krankheitserreger an Pflanzen | |
DE4109093A1 (de) | Mittel zur umweltfreundlichen und gesundheitlich unbedenklicheren konservierung von citrusfruechten | |
DE4132270A1 (de) | Verfahren zur vorbehandlung von saatgut, insbesondere solches von forstgehoelzen | |
DE321317C (de) | Mittel zur Vertilgung von Insekten und sonstigen auf Tieren oder Pflanzen wohnenden Parasiten | |
DE2545150C2 (de) | Fungicide Zusammensetzungen |