DD151867A5 - Formulierung fuer landwirtschaftliche zwecke - Google Patents
Formulierung fuer landwirtschaftliche zwecke Download PDFInfo
- Publication number
- DD151867A5 DD151867A5 DD80220842A DD22084280A DD151867A5 DD 151867 A5 DD151867 A5 DD 151867A5 DD 80220842 A DD80220842 A DD 80220842A DD 22084280 A DD22084280 A DD 22084280A DD 151867 A5 DD151867 A5 DD 151867A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- effect
- fruit set
- plant species
- oil
- compounds
- Prior art date
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- 239000003759 ester based solvent Substances 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- CYEBJEDOHLIWNP-UHFFFAOYSA-N methanethioamide Chemical compound NC=S CYEBJEDOHLIWNP-UHFFFAOYSA-N 0.000 description 1
- OUIKGSFQDXMVFW-UHFFFAOYSA-N methanethioamide methylhydrazine Chemical class C(=S)N.CNN OUIKGSFQDXMVFW-UHFFFAOYSA-N 0.000 description 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
- ACPCUSFQAIOMAS-UHFFFAOYSA-N methyl 2-carbonochloridoyl-3-methylbenzoate Chemical compound COC(=O)C1=CC=CC(C)=C1C(Cl)=O ACPCUSFQAIOMAS-UHFFFAOYSA-N 0.000 description 1
- RPRRVPFLMJGXOQ-UHFFFAOYSA-N methyl N-(1,3-dioxoisoindol-2-yl)-N'-(3-fluorophenyl)-N-methylcarbamimidothioate Chemical compound CN(C(SC)=NC1=CC(=CC=C1)F)N1C(C2=CC=CC=C2C1=O)=O RPRRVPFLMJGXOQ-UHFFFAOYSA-N 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- GWJYYOWGLLHNRJ-UHFFFAOYSA-N n-hydrazinylmethanethioamide Chemical compound NNNC=S GWJYYOWGLLHNRJ-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000004018 waxing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
- C07D317/66—Nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3587579A | 1979-05-03 | 1979-05-03 | |
| US06/133,888 US4292071A (en) | 1979-05-03 | 1980-04-10 | Isothioureido isoindolediones and use as plant growth regulators |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD151867A5 true DD151867A5 (de) | 1981-11-11 |
Family
ID=26712579
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD80220842A DD151867A5 (de) | 1979-05-03 | 1980-05-02 | Formulierung fuer landwirtschaftliche zwecke |
| DD80230461A DD159332A5 (de) | 1979-05-03 | 1980-05-02 | Verfahren zur herstellung von neuen isothioureidoisoindoldionen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD80230461A DD159332A5 (de) | 1979-05-03 | 1980-05-02 | Verfahren zur herstellung von neuen isothioureidoisoindoldionen |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4292071A (https=) |
| AT (1) | AT366665B (https=) |
| AU (1) | AU5756080A (https=) |
| BR (1) | BR8002705A (https=) |
| DD (2) | DD151867A5 (https=) |
| DK (1) | DK194380A (https=) |
| FI (1) | FI801378A7 (https=) |
| GB (1) | GB2049678B (https=) |
| GR (1) | GR68106B (https=) |
| PT (1) | PT71132B (https=) |
| YU (1) | YU117480A (https=) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4339382A (en) * | 1980-02-11 | 1982-07-13 | Gulf Oil Corporation | Process for manufacturing N-arylthiocarbamoyl-2-amino-1H-isoindole-1,3-(2H)diones |
| CN103113300A (zh) * | 2013-03-06 | 2013-05-22 | 广西中医药大学 | 一种具有抗肿瘤活性的化合物的制备方法和用途 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2661350A (en) * | 1952-10-22 | 1953-12-01 | Schenley Ind Inc | Isothiuronium salt of penicillin |
| US2872450A (en) * | 1955-12-06 | 1959-02-03 | Bayer Ag | Thio- and dithio-carboxylic acid esters and a process for their manufacture |
| DE1174103B (de) | 1961-09-22 | 1964-07-16 | Philips Nv | Mittel zur Bekaempfung von Schimmelpilzen auf lebenden Pflanzen |
| FR1439872A (fr) * | 1964-12-22 | 1966-05-27 | Roussel Uclaf | Nouveaux composés dithiocarbamiques et procédé de préparation |
| DE1567153C3 (de) * | 1965-08-11 | 1974-08-29 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Neue N-Carbamoyloxydicarbonsäureimide |
| GB1272920A (en) | 1971-03-15 | 1972-05-03 | Berlin Chemie Veb | New thiosemicarbazides |
-
1980
- 1980-04-10 US US06/133,888 patent/US4292071A/en not_active Expired - Lifetime
- 1980-04-17 AU AU57560/80A patent/AU5756080A/en not_active Abandoned
- 1980-04-23 PT PT71132A patent/PT71132B/pt unknown
- 1980-04-28 GR GR61797A patent/GR68106B/el unknown
- 1980-04-29 FI FI801378A patent/FI801378A7/fi not_active Application Discontinuation
- 1980-04-30 GB GB8014259A patent/GB2049678B/en not_active Expired
- 1980-04-30 AT AT0231880A patent/AT366665B/de not_active IP Right Cessation
- 1980-04-30 YU YU01174/80A patent/YU117480A/xx unknown
- 1980-05-01 DK DK194380A patent/DK194380A/da unknown
- 1980-05-02 BR BR8002705A patent/BR8002705A/pt unknown
- 1980-05-02 DD DD80220842A patent/DD151867A5/de unknown
- 1980-05-02 DD DD80230461A patent/DD159332A5/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GR68106B (https=) | 1981-10-30 |
| YU117480A (en) | 1983-02-28 |
| PT71132A (en) | 1980-06-01 |
| PT71132B (en) | 1983-01-10 |
| FI801378A7 (fi) | 1980-11-04 |
| DK194380A (da) | 1980-11-04 |
| AT366665B (de) | 1982-04-26 |
| ATA231880A (de) | 1981-09-15 |
| AU5756080A (en) | 1980-11-06 |
| BR8002705A (pt) | 1980-12-16 |
| GB2049678B (en) | 1983-09-07 |
| GB2049678A (en) | 1980-12-31 |
| US4292071A (en) | 1981-09-29 |
| DD159332A5 (de) | 1983-03-02 |
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