CH433858A - Verwendung von organischen Phosphorverbindungen - Google Patents
Verwendung von organischen PhosphorverbindungenInfo
- Publication number
- CH433858A CH433858A CH436663A CH436663A CH433858A CH 433858 A CH433858 A CH 433858A CH 436663 A CH436663 A CH 436663A CH 436663 A CH436663 A CH 436663A CH 433858 A CH433858 A CH 433858A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- propyl
- phthalimidomethyl
- ethyl
- phosphorodithioate
- Prior art date
Links
- 150000002903 organophosphorus compounds Chemical class 0.000 title claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 241000607479 Yersinia pestis Species 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052717 sulfur Chemical group 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 241000238631 Hexapoda Species 0.000 description 5
- 241000257159 Musca domestica Species 0.000 description 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 241000238675 Periplaneta americana Species 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000009885 systemic effect Effects 0.000 description 4
- 241000238876 Acari Species 0.000 description 3
- 241000255925 Diptera Species 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- 230000000895 acaricidal effect Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- JKGLRGGCGUQNEX-UHFFFAOYSA-N 2-(chloromethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCl)C(=O)C2=C1 JKGLRGGCGUQNEX-UHFFFAOYSA-N 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 241000258913 Oncopeltus fasciatus Species 0.000 description 1
- 241000118205 Ovicides Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- -1 ester phosphorodithioate salts Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/5537—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom the heteroring containing the structure -C(=O)-N-C(=O)- (both carbon atoms belong to the heteroring)
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18683862A | 1962-04-12 | 1962-04-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH433858A true CH433858A (de) | 1967-04-15 |
Family
ID=22686460
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH436663A CH433858A (de) | 1962-04-12 | 1963-04-05 | Verwendung von organischen Phosphorverbindungen |
| CH192267A CH434257A (de) | 1962-04-12 | 1963-04-05 | Verfahren zur Herstellung von organischen Phosphorverbindungen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH192267A CH434257A (de) | 1962-04-12 | 1963-04-05 | Verfahren zur Herstellung von organischen Phosphorverbindungen |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE630933A (ja) |
| BR (1) | BR6348350D0 (ja) |
| CH (2) | CH433858A (ja) |
| NL (1) | NL291405A (ja) |
-
0
- BE BE630933D patent/BE630933A/xx unknown
- NL NL291405D patent/NL291405A/xx unknown
-
1963
- 1963-04-05 CH CH436663A patent/CH433858A/de unknown
- 1963-04-05 CH CH192267A patent/CH434257A/de unknown
- 1963-04-10 BR BR14835063A patent/BR6348350D0/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR6348350D0 (pt) | 1973-06-26 |
| NL291405A (ja) | |
| CH434257A (de) | 1967-04-30 |
| BE630933A (ja) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1567137C3 (de) | Insektizides Mittel auf der Basis von Phosphorsäureisoxazolyiestern | |
| DE944430C (de) | Verfahren zur Herstellung biologisch bzw. insektizid wirksamer Phosphor-, Arsen- oder Antimon-Verbindungen | |
| DE1768147A1 (de) | Phosphor- und Phosphonsaeureacetylhydrazide mit pestizider Wirkung und Verfahren zu ihrer Herstellung | |
| DE1062237B (de) | Verfahren zur Herstellung von O, O-Dialkylthiolphosphorsaeure- und -thiolthionophosphorsaeure-S-gamma-cyanallylestern | |
| DE2338847A1 (de) | Insektizid, insbesondere mit selektiver kaefertoetender wirkung | |
| CH433858A (de) | Verwendung von organischen Phosphorverbindungen | |
| DE1017848B (de) | Insektizide Mittel | |
| DE1147439B (de) | Phosphorsaeureester als insektizide Mittel | |
| DE1618435A1 (de) | Schaedlingsbekaempfungsmittel mit Aryl- und Aralkyl-omega-alkinyl-phosphonsaeureestern als Synergist | |
| DE1593558A1 (de) | Ungeziefervertilgungsmittel | |
| CH627620A5 (en) | Method and composition for controlling insects and acarids | |
| US3242498A (en) | Carbamyl phosphates | |
| US3073858A (en) | 2(o-alkyl-alkylphosphonodithioyl)-ethyl carbamates | |
| DE1693180C (de) | Phosphor schwefelhaltige Athylcarba | |
| DE2041627C3 (de) | Pestizide Mittel | |
| DE2209799C3 (de) | Verfahren zur Herstellung von Thiophosphorsäurevinylestern | |
| AT264206B (de) | Insektizides Mittel | |
| CH391726A (de) | Verfahren zur Herstellung von neuen Phosphonaten und deren Verwendung | |
| US3351680A (en) | Omicron, omicron-diloweralkyl phosphorodithioyl-methyl-substituted mercaptoacetates | |
| DE1245977B (de) | Verfahren zur Herstellung von 1,3,2-Benzodioxaphosphoranen | |
| DE1518675C3 (de) | N-Methyl-carbamate und Verfahren zu deren Herstellung sowie diese enthaltende Schäd lingsbekämpfungsmittel | |
| US3247052A (en) | Thiocarbonyldi (omicron, omicron-diethyl-phosphonate) in an insecticidal method | |
| DE1935758C (de) | (Thio) Phosphonsaureester und ihre Verwendung als Wirkstoffe in Schädlings bekampfungsmitteln | |
| DE1939418C (de) | 0,5 (2 Methyl pyridyl) phosphorverbin düngen | |
| AT222941B (de) | Parasitentötende Präparate |