MD1721Z - Применение (Z)-1-(2,4-дихлорфенил)-5-метил-2-(1H-1,2,4-триазол-1-ил)гекс-1-ен-3-она в качестве активного соединения против гриба Gloeosporium ampelophagum Sacc. - Google Patents
Применение (Z)-1-(2,4-дихлорфенил)-5-метил-2-(1H-1,2,4-триазол-1-ил)гекс-1-ен-3-она в качестве активного соединения против гриба Gloeosporium ampelophagum Sacc. Download PDFInfo
- Publication number
- MD1721Z MD1721Z MDS20220097A MDS20220097A MD1721Z MD 1721 Z MD1721 Z MD 1721Z MD S20220097 A MDS20220097 A MD S20220097A MD S20220097 A MDS20220097 A MD S20220097A MD 1721 Z MD1721 Z MD 1721Z
- Authority
- MD
- Moldova
- Prior art keywords
- ampelophagum
- gloeosporium
- sacc
- dichlorophenyl
- methyl
- Prior art date
Links
- 241000901048 Elsinoe ampelina Species 0.000 title claims abstract description 11
- 150000001875 compounds Chemical class 0.000 title claims abstract description 8
- RHRSEZQUWLVSHO-NSIKDUERSA-N (z)-1-(2,4-dichlorophenyl)-5-methyl-2-(1,2,4-triazol-1-yl)hex-1-en-3-one Chemical compound C1=NC=NN1/C(C(=O)CC(C)C)=C\C1=CC=C(Cl)C=C1Cl RHRSEZQUWLVSHO-NSIKDUERSA-N 0.000 title claims abstract description 6
- 241000233866 Fungi Species 0.000 title abstract description 4
- 239000000417 fungicide Substances 0.000 abstract description 6
- 235000014787 Vitis vinifera Nutrition 0.000 abstract description 4
- 240000006365 Vitis vinifera Species 0.000 abstract description 3
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 abstract description 2
- 231100000676 disease causative agent Toxicity 0.000 abstract description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 description 22
- 201000010099 disease Diseases 0.000 description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 8
- 230000001717 pathogenic effect Effects 0.000 description 6
- 150000003852 triazoles Chemical group 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 244000052769 pathogen Species 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 230000035784 germination Effects 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 235000015097 nutrients Nutrition 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 230000000843 anti-fungal effect Effects 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
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- 238000009369 viticulture Methods 0.000 description 3
- 241000219094 Vitaceae Species 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
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- 235000021021 grapes Nutrition 0.000 description 2
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- 238000002955 isolation Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 1
- YSFBEAASFUWWHU-UHFFFAOYSA-N 2,4-dichlorobenzaldehyde Chemical compound ClC1=CC=C(C=O)C(Cl)=C1 YSFBEAASFUWWHU-UHFFFAOYSA-N 0.000 description 1
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 description 1
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 description 1
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 239000005802 Mancozeb Substances 0.000 description 1
- 239000005809 Metiram Substances 0.000 description 1
- 239000005811 Myclobutanil Substances 0.000 description 1
- 239000005822 Propiconazole Substances 0.000 description 1
- 239000005840 Tetraconazole Substances 0.000 description 1
- 241000219095 Vitis Species 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000844 anti-bacterial effect Effects 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
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000011905 homologation Methods 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- AFCCDDWKHLHPDF-UHFFFAOYSA-M metam-sodium Chemical compound [Na+].CNC([S-])=S AFCCDDWKHLHPDF-UHFFFAOYSA-M 0.000 description 1
- 229920000257 metiram Polymers 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000001965 potato dextrose agar Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000004763 spore germination Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000004808 supercritical fluid chromatography Methods 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Изобретение относится к химии и сельскому хозяйству, в частности к применению гетероциклического соединения, производного 1,2,4-триазола, в качестве фунгицидного средства для борьбы с антракнозом, вызванным Gloeosporium ampelophagum Sacc. Сущность изобретения состоит в том, что в качестве активного соединения против гриба Gloeosporium ampelophagum Sacc. - возбудитель антракноза винограда, предлагается (Z)-1-(2,4-дихлорфенил)-5-метил-2-(1H-1,2,4-триазол-1-ил)гекс-1-ен-3-он с формулой:. Оптимальная активная концентрация равна 0,05%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDS20220097A MD1721Z (ru) | 2022-11-30 | 2022-11-30 | Применение (Z)-1-(2,4-дихлорфенил)-5-метил-2-(1H-1,2,4-триазол-1-ил)гекс-1-ен-3-она в качестве активного соединения против гриба Gloeosporium ampelophagum Sacc. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDS20220097A MD1721Z (ru) | 2022-11-30 | 2022-11-30 | Применение (Z)-1-(2,4-дихлорфенил)-5-метил-2-(1H-1,2,4-триазол-1-ил)гекс-1-ен-3-она в качестве активного соединения против гриба Gloeosporium ampelophagum Sacc. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MD1721Y MD1721Y (ru) | 2023-10-31 |
| MD1721Z true MD1721Z (ru) | 2024-05-31 |
Family
ID=88599002
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MDS20220097A MD1721Z (ru) | 2022-11-30 | 2022-11-30 | Применение (Z)-1-(2,4-дихлорфенил)-5-метил-2-(1H-1,2,4-триазол-1-ил)гекс-1-ен-3-она в качестве активного соединения против гриба Gloeosporium ampelophagum Sacc. |
Country Status (1)
| Country | Link |
|---|---|
| MD (1) | MD1721Z (ru) |
-
2022
- 2022-11-30 MD MDS20220097A patent/MD1721Z/ru active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| MD1721Y (ru) | 2023-10-31 |
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| FG9Y | Short term patent issued |