IL29429A - Phosphoric,phosphonic and thionophosphoric(-phosphonic)acid quinoxalyl-(6) esters - Google Patents
Phosphoric,phosphonic and thionophosphoric(-phosphonic)acid quinoxalyl-(6) estersInfo
- Publication number
- IL29429A IL29429A IL2942968A IL2942968A IL29429A IL 29429 A IL29429 A IL 29429A IL 2942968 A IL2942968 A IL 2942968A IL 2942968 A IL2942968 A IL 2942968A IL 29429 A IL29429 A IL 29429A
- Authority
- IL
- Israel
- Prior art keywords
- ester
- formula
- phosphoric
- esters
- phosphonic
- Prior art date
Links
- 150000002148 esters Chemical class 0.000 title claims description 23
- 239000002253 acid Substances 0.000 title claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 48
- 238000000034 method Methods 0.000 claims description 18
- 241000238631 Hexapoda Species 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 14
- -1 ester halide Chemical class 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 239000003085 diluting agent Substances 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 230000000749 insecticidal effect Effects 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- RQPVXTQTNVVKEJ-UHFFFAOYSA-N quinoxalin-6-ol Chemical compound N1=CC=NC2=CC(O)=CC=C21 RQPVXTQTNVVKEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 239000012442 inert solvent Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 12
- 241000238876 Acari Species 0.000 description 9
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- 239000003995 emulsifying agent Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 230000000895 acaricidal effect Effects 0.000 description 6
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- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
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- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- HGELWZQRZUOEOJ-UHFFFAOYSA-N ethyl-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCP(O)(O)=S HGELWZQRZUOEOJ-UHFFFAOYSA-N 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
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- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
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- YFBUDXNMBTUSOC-UHFFFAOYSA-N 1,4-dihydroquinoxaline-2,3-dithione Chemical class C1=CC=C2NC(=S)C(=S)NC2=C1 YFBUDXNMBTUSOC-UHFFFAOYSA-N 0.000 description 1
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- 241001513837 Dermestes maculatus Species 0.000 description 1
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- 241000255601 Drosophila melanogaster Species 0.000 description 1
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- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
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- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
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- 241000690748 Piesma Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- 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
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/650952—Six-membered rings having the nitrogen atoms in the positions 1 and 4
- C07F9/650994—Six-membered rings having the nitrogen atoms in the positions 1 and 4 condensed with carbocyclic rings or carbocyclic ring systems
-
- 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
- A01N57/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34
- A01N57/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34 containing aromatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0051761 | 1967-03-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL29429A true IL29429A (en) | 1971-06-23 |
Family
ID=7104883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL2942968A IL29429A (en) | 1967-03-09 | 1968-02-07 | Phosphoric,phosphonic and thionophosphoric(-phosphonic)acid quinoxalyl-(6) esters |
Country Status (8)
| Country | Link |
|---|---|
| BE (1) | BE711819A (en)van) |
| CH (1) | CH493562A (en)van) |
| DE (1) | DE1670817B2 (en)van) |
| ES (1) | ES351428A1 (en)van) |
| FR (1) | FR1575612A (en)van) |
| GB (1) | GB1160493A (en)van) |
| IL (1) | IL29429A (en)van) |
| NL (1) | NL6803253A (en)van) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2410311A1 (de) * | 1974-03-05 | 1975-09-18 | Bayer Ag | Bromhaltige chinoxalyl-(thiono)-(thiol)- phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
-
1967
- 1967-03-09 DE DE19671670817 patent/DE1670817B2/de active Granted
-
1968
- 1968-02-05 CH CH165368A patent/CH493562A/de not_active IP Right Cessation
- 1968-02-07 IL IL2942968A patent/IL29429A/en unknown
- 1968-02-13 GB GB696868A patent/GB1160493A/en not_active Expired
- 1968-03-07 BE BE711819D patent/BE711819A/xx unknown
- 1968-03-07 NL NL6803253A patent/NL6803253A/xx unknown
- 1968-03-08 FR FR1575612D patent/FR1575612A/fr not_active Expired
- 1968-03-09 ES ES351428A patent/ES351428A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES351428A1 (es) | 1969-06-16 |
| DE1670817C3 (en)van) | 1975-04-03 |
| DE1670817B2 (de) | 1974-08-01 |
| NL6803253A (en)van) | 1968-09-10 |
| BE711819A (en)van) | 1968-09-09 |
| FR1575612A (en)van) | 1969-07-25 |
| GB1160493A (en) | 1969-08-06 |
| CH493562A (de) | 1970-07-15 |
| DE1670817A1 (de) | 1971-04-01 |
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