AT233323B - Fungizide Mittel - Google Patents
Fungizide MittelInfo
- Publication number
- AT233323B AT233323B AT238762A AT238762A AT233323B AT 233323 B AT233323 B AT 233323B AT 238762 A AT238762 A AT 238762A AT 238762 A AT238762 A AT 238762A AT 233323 B AT233323 B AT 233323B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- halogen
- hydrogen
- fungicides
- alkyl
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 150000002431 hydrogen Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- -1 nitro, hydroxyl Chemical group 0.000 claims 2
- 101100006370 Arabidopsis thaliana CHX2 gene Proteins 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000004442 acylamino group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 230000002538 fungal effect Effects 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- 125000006519 CCH3 Chemical group 0.000 description 1
- 101001003232 Mus musculus Immediate early response gene 2 protein Proteins 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- REQPQFUJGGOFQL-UHFFFAOYSA-N dimethylcarbamothioyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SC(=S)N(C)C REQPQFUJGGOFQL-UHFFFAOYSA-N 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
<Desc/Clms Page number 1> Fungizide Mittel EMI1.1 <Desc/Clms Page number 2> =CHX1 = kein Pilzwachstum 2 = geringes Pilzwachstum 3 = mittleres Pilzwachstum 4 = starkes Pilzwachstum 5 = Pilzdecke geschlossen Wirkung gegenüber Aspergillus niger : EMI2.1 <tb> <tb> Wirkstoff <SEP> Wirkstoffgehalt <SEP> der <SEP> Talkummischung <SEP> in <SEP> % <tb> 0,01 <SEP> 0,019 <SEP> 0,038 <SEP> 0,075 <SEP> 0,15 <SEP> 0,31 <SEP> 0,63 <SEP> 1,25 <SEP> 2,5 <SEP> 5,0 <tb> CH2=CH. <SEP> SO2.O.R <tb> R <SEP> =# <SEP> 5 <SEP> 5 <SEP> 3 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> # <SEP> 4 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> Cl. <tb> #-CH3 <SEP> 5 <SEP> 4 <SEP> 3 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> CH3 <tb> C-CH3 <SEP> 5 <SEP> 5 <SEP> 4 <SEP> 4 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> CH3 <tb> # <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 4 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> H <SEP> 5 <SEP> 4 <SEP> 4 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> Pentachlorphenol <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> 3, <SEP> 5-Dimethyl-tetrahydro- <tb> - <SEP> l, <SEP> 3, <SEP> 5-thiadiazin-2-thion <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> l-Nitro-3, <SEP> 5-Rhodanbenzol <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 2 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb> Zink-dimethyl-dithiocarbamat <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 4 <SEP> 3 <SEP> 1 <SEP> 1 <tb> Tetramethyl-thiuramidsulfid <SEP> 5. <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 3 <SEP> 2 <SEP> 2 <SEP> 2 <tb> Mangan-äthylen-bis- <tb> - <SEP> dithiocarbamat <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 5 <SEP> 3 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <SEP> 1 <tb>
Claims (1)
- PATENTANSPRUCH : Fungizide Mittel, gekennzeichnet durch einen Gehalt an Verbindungen der Formel Ar-OSO2-CX1=CHX2, in der Ar einen aromatischen Rest, der gegebenenfalls durch einen oder mehrere Halogen-, Alkyl-, Nitro-, Hydroxyl-, Acyl-, Formyl-, Methoxy-, Äthoxy-, Nitril-, Acylamino- oder Rhodanreste substituiert sein kann, X Wasserstoff, einen Alkylrest oder Halogen und X2 Wasserstoff, einen Alkylrest oder Halogen bedeutet.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE233323X | 1961-03-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT233323B true AT233323B (de) | 1964-05-11 |
Family
ID=5885522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT238762A AT233323B (de) | 1961-03-24 | 1962-03-23 | Fungizide Mittel |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT233323B (de) |
-
1962
- 1962-03-23 AT AT238762A patent/AT233323B/de active
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