CH625397A5 - - Google Patents
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- Publication number
- CH625397A5 CH625397A5 CH83977A CH83977A CH625397A5 CH 625397 A5 CH625397 A5 CH 625397A5 CH 83977 A CH83977 A CH 83977A CH 83977 A CH83977 A CH 83977A CH 625397 A5 CH625397 A5 CH 625397A5
- Authority
- CH
- Switzerland
- Prior art keywords
- spp
- propyl
- ethyl
- butyl
- alkyl
- Prior art date
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- 150000001875 compounds Chemical class 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 22
- 238000002360 preparation method Methods 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 12
- 238000009472 formulation Methods 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 claims description 8
- 230000000895 acaricidal effect Effects 0.000 claims description 7
- 239000002253 acid Substances 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
- 125000004414 alkyl thio group Chemical group 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 230000001069 nematicidal effect Effects 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 229910052717 sulfur Chemical group 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 4
- 125000003282 alkyl amino group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
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- 125000005843 halogen group Chemical group 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
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- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
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- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
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- 125000000129 anionic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
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- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
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- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
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- 238000001035 drying Methods 0.000 description 1
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- 150000008282 halocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052742 iron Inorganic materials 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
- 150000002576 ketones Chemical class 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/28—Cinnolines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D237/20—Nitrogen atoms
-
- 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
- C07F9/650905—Six-membered rings having the nitrogen atoms in the positions 1 and 2
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2603052A DE2603052A1 (de) | 1976-01-28 | 1976-01-28 | S- eckige klammer auf 1,6-dihydro- 6-thioxo-pyridazin-(1)ylmethyl eckige klammer zu -(thiono)-(di)-thiol-phopshor(phosphon)- saeureester- bzw. -esteramidderivate, verfahren zur ihrer herstellung und ihre verwendung als insektizide, akarizide und nematizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH625397A5 true CH625397A5 (ro) | 1981-09-30 |
Family
ID=5968406
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH83977A CH625397A5 (ro) | 1976-01-28 | 1977-01-24 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4097593A (ro) |
| JP (1) | JPS5291884A (ro) |
| AT (1) | AT350324B (ro) |
| AU (1) | AU503845B2 (ro) |
| BE (1) | BE850798A (ro) |
| BR (1) | BR7700494A (ro) |
| CH (1) | CH625397A5 (ro) |
| CS (2) | CS191350B2 (ro) |
| DD (1) | DD128688A5 (ro) |
| DE (1) | DE2603052A1 (ro) |
| DK (1) | DK141334C (ro) |
| FR (1) | FR2339619A1 (ro) |
| GB (1) | GB1521952A (ro) |
| IL (1) | IL51324A (ro) |
| NL (1) | NL7700792A (ro) |
| PL (1) | PL101197B1 (ro) |
| PT (1) | PT66103B (ro) |
| SE (1) | SE7700853L (ro) |
| TR (1) | TR19269A (ro) |
| ZA (1) | ZA77479B (ro) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2843823A1 (de) | 1978-10-07 | 1980-04-24 | Bayer Ag | N-iso-propyl-s-(1,6-dihydro-6-(thi) oxo- pyriezin(1)-yl-methyl)-thiolphosphorsaeure- esteramide, verfahren zu ihrer herstellung und ihre anwendung als schaedlingsbekaempfungsmittel |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2938902A (en) * | 1959-04-24 | 1960-05-31 | American Cyanamid Co | Novel pyridazinones and methods of preparing same |
| CH547313A (de) * | 1968-02-02 | 1974-03-29 | Bayer Ag | Verfahren zur herstellung von phosphor-, phosphon-thionphosphor- oder thionsphosphonsaeureestern- bezw.-esteramiden. |
| DE2046088A1 (de) * | 1970-09-18 | 1972-03-30 | Farbenfabriken Bayer Ag, 5090 Lever Kusen | Cinnolinyl(thiono)phosphor(phosphon) säureester und esteramide, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Insektizide und Akanzide |
| DE2316821A1 (de) | 1973-04-04 | 1974-10-17 | Bayer Ag | S- eckige klammer auf 1,6-dihydro-6oxo-pyridazin-(1)ylmethyl eckige klammer zu -(thiono)-(di)-thiol-phosphor(phosphon)saeureester- bzw. -esteramidderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide und nematizide |
| DE2348736A1 (de) * | 1973-09-28 | 1975-04-10 | Bayer Ag | S- eckige klammer auf 1,6-dihydropyridazin-(1)-ylmethyl eckige klammer zu -thiolphosphorsaeureester- bzw. -esteramidderivate, verfahren zu ihrer herstellung sowie ihre verwendung als nematizide |
-
1976
- 1976-01-28 DE DE2603052A patent/DE2603052A1/de not_active Withdrawn
-
1977
- 1977-01-10 US US05/758,242 patent/US4097593A/en not_active Expired - Lifetime
- 1977-01-21 PT PT66103A patent/PT66103B/pt unknown
- 1977-01-24 CH CH83977A patent/CH625397A5/de not_active IP Right Cessation
- 1977-01-25 TR TR19269A patent/TR19269A/xx unknown
- 1977-01-25 IL IL51324A patent/IL51324A/xx unknown
- 1977-01-25 CS CS781679A patent/CS191350B2/cs unknown
- 1977-01-25 CS CS77506A patent/CS191327B2/cs unknown
- 1977-01-25 GB GB2964/77A patent/GB1521952A/en not_active Expired
- 1977-01-26 NL NL7700792A patent/NL7700792A/xx not_active Application Discontinuation
- 1977-01-26 DD DD7700197100A patent/DD128688A5/xx unknown
- 1977-01-26 JP JP689077A patent/JPS5291884A/ja active Pending
- 1977-01-26 AU AU21679/77A patent/AU503845B2/en not_active Expired
- 1977-01-27 PL PL1977195606A patent/PL101197B1/pl unknown
- 1977-01-27 DK DK34377A patent/DK141334C/da active
- 1977-01-27 SE SE7700853A patent/SE7700853L/xx unknown
- 1977-01-27 BR BR7700494A patent/BR7700494A/pt unknown
- 1977-01-27 BE BE174414A patent/BE850798A/xx unknown
- 1977-01-27 ZA ZA770479A patent/ZA77479B/xx unknown
- 1977-01-28 FR FR7702490A patent/FR2339619A1/fr active Granted
- 1977-01-28 AT AT53377A patent/AT350324B/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IL51324A0 (en) | 1977-03-31 |
| DE2603052A1 (de) | 1977-08-04 |
| DD128688A5 (de) | 1977-12-07 |
| JPS5291884A (en) | 1977-08-02 |
| BE850798A (fr) | 1977-07-27 |
| FR2339619B1 (ro) | 1980-07-11 |
| ZA77479B (en) | 1977-12-28 |
| SE7700853L (sv) | 1977-07-29 |
| CS191350B2 (en) | 1979-06-29 |
| GB1521952A (en) | 1978-08-23 |
| DK34377A (da) | 1977-07-29 |
| PT66103B (de) | 1978-06-27 |
| FR2339619A1 (fr) | 1977-08-26 |
| TR19269A (tr) | 1978-10-06 |
| DK141334C (da) | 1980-08-18 |
| BR7700494A (pt) | 1977-10-04 |
| CS191327B2 (en) | 1979-06-29 |
| PT66103A (de) | 1977-02-01 |
| AU2167977A (en) | 1978-08-03 |
| US4097593A (en) | 1978-06-27 |
| IL51324A (en) | 1979-11-30 |
| PL101197B1 (pl) | 1978-12-30 |
| DK141334B (da) | 1980-02-25 |
| AT350324B (de) | 1979-05-25 |
| AU503845B2 (en) | 1979-09-20 |
| NL7700792A (nl) | 1977-08-01 |
| ATA53377A (de) | 1978-10-15 |
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| Date | Code | Title | Description |
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| PL | Patent ceased |