IL34448A - Phosphoric,thionophosphoric,phosphonic and thionophosphonic acid esters,ester amides and diamides,their production and their use as insecticides,acaricides and fungicides - Google Patents
Phosphoric,thionophosphoric,phosphonic and thionophosphonic acid esters,ester amides and diamides,their production and their use as insecticides,acaricides and fungicidesInfo
- Publication number
- IL34448A IL34448A IL34448A IL3444870A IL34448A IL 34448 A IL34448 A IL 34448A IL 34448 A IL34448 A IL 34448A IL 3444870 A IL3444870 A IL 3444870A IL 34448 A IL34448 A IL 34448A
- Authority
- IL
- Israel
- Prior art keywords
- compound
- formula
- carbon atoms
- active compound
- alkyl
- Prior art date
Links
- -1 ester amides Chemical class 0.000 title claims description 23
- 239000002253 acid Substances 0.000 title claims description 17
- 230000000895 acaricidal effect Effects 0.000 title claims description 8
- 150000002148 esters Chemical class 0.000 title claims description 7
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 150000001470 diamides Chemical class 0.000 title claims description 3
- 239000000417 fungicide Substances 0.000 title description 3
- 239000002917 insecticide Substances 0.000 title description 3
- 239000000642 acaricide Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 153
- 230000006378 damage Effects 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 12
- 241000238631 Hexapoda Species 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 239000003085 diluting agent Substances 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 9
- 241000607479 Yersinia pestis Species 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 230000000749 insecticidal effect Effects 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 241000233866 Fungi Species 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- 230000000855 fungicidal effect Effects 0.000 claims description 4
- 239000011734 sodium Chemical group 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- DYUMBFTYRJMAFK-UHFFFAOYSA-N 3-cyano-2-pyridone Chemical class OC1=NC=CC=C1C#N DYUMBFTYRJMAFK-UHFFFAOYSA-N 0.000 claims description 3
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- 239000004094 surface-active agent Substances 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000005864 Sulphur Chemical group 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims description 2
- 244000045947 parasite Species 0.000 claims description 2
- 239000011591 potassium Chemical group 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
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- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 2
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000000974 larvacidal effect Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 201000004792 malaria Diseases 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 150000003008 phosphonic acid esters Chemical class 0.000 description 1
- FUWGSUOSJRCEIV-UHFFFAOYSA-N phosphonothioic O,O-acid Chemical class OP(O)=S FUWGSUOSJRCEIV-UHFFFAOYSA-N 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
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
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/58—Pyridine rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19691927643 DE1927643A1 (de) | 1969-05-30 | 1969-05-30 | Phosphor-(Phosphon)- bzw. Thionophosphor-(phosphon)-saeureester,-esteramide bzw. -diamide,Verfahren zu ihrer Herstellung sowie ihre Verwendung als Insektizide,Akarizide und Fungizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL34448A0 IL34448A0 (en) | 1970-07-19 |
| IL34448A true IL34448A (en) | 1973-01-30 |
Family
ID=5735668
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL34448A IL34448A (en) | 1969-05-30 | 1970-05-04 | Phosphoric,thionophosphoric,phosphonic and thionophosphonic acid esters,ester amides and diamides,their production and their use as insecticides,acaricides and fungicides |
Country Status (15)
| Country | Link |
|---|---|
| JP (2) | JPS526342B1 (ja) |
| AT (1) | AT297027B (ja) |
| BE (1) | BE751171A (ja) |
| CH (1) | CH498157A (ja) |
| CS (1) | CS161749B2 (ja) |
| DE (1) | DE1927643A1 (ja) |
| DK (1) | DK128121B (ja) |
| ES (1) | ES380220A1 (ja) |
| FR (1) | FR2043833A1 (ja) |
| GB (1) | GB1263652A (ja) |
| IL (1) | IL34448A (ja) |
| NL (1) | NL7007733A (ja) |
| PL (1) | PL69776B1 (ja) |
| RO (1) | RO58847A (ja) |
| SU (1) | SU460631A3 (ja) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3445465A1 (de) * | 1984-12-13 | 1986-06-19 | Bayer Ag, 5090 Leverkusen | Pyrimidinyl-thionophosphorsaeureester |
-
1969
- 1969-05-30 DE DE19691927643 patent/DE1927643A1/de active Pending
-
1970
- 1970-05-01 CH CH660070A patent/CH498157A/de not_active IP Right Cessation
- 1970-05-04 IL IL34448A patent/IL34448A/en unknown
- 1970-05-14 RO RO63358A patent/RO58847A/ro unknown
- 1970-05-28 JP JP45045255A patent/JPS526342B1/ja active Pending
- 1970-05-28 JP JP45045254A patent/JPS4817277B1/ja active Pending
- 1970-05-28 NL NL7007733A patent/NL7007733A/xx unknown
- 1970-05-29 GB GB26028/70A patent/GB1263652A/en not_active Expired
- 1970-05-29 SU SU1443808A patent/SU460631A3/ru active
- 1970-05-29 BE BE751171D patent/BE751171A/xx unknown
- 1970-05-29 DK DK278870AA patent/DK128121B/da unknown
- 1970-05-29 CS CS3788A patent/CS161749B2/cs unknown
- 1970-05-29 FR FR7019721A patent/FR2043833A1/fr not_active Withdrawn
- 1970-05-29 PL PL1970140959A patent/PL69776B1/pl unknown
- 1970-05-29 AT AT481470A patent/AT297027B/de not_active IP Right Cessation
- 1970-05-30 ES ES380220A patent/ES380220A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES380220A1 (es) | 1972-08-16 |
| CS161749B2 (ja) | 1975-06-10 |
| CH498157A (de) | 1970-10-31 |
| DK128121B (da) | 1974-03-04 |
| NL7007733A (ja) | 1970-12-02 |
| PL69776B1 (ja) | 1973-08-31 |
| GB1263652A (en) | 1972-02-16 |
| FR2043833A1 (ja) | 1971-02-19 |
| IL34448A0 (en) | 1970-07-19 |
| JPS4817277B1 (ja) | 1973-05-28 |
| SU460631A3 (ru) | 1975-02-15 |
| RO58847A (ja) | 1976-03-15 |
| JPS526342B1 (ja) | 1977-02-21 |
| AT297027B (de) | 1972-03-10 |
| DE1927643A1 (de) | 1970-12-03 |
| BE751171A (fr) | 1970-11-30 |
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