DE2455680A1 - Substituierte carboxylmethyl(di) thiol(thiono)-phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide, akarizide und nematizide - Google Patents
Substituierte carboxylmethyl(di) thiol(thiono)-phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide, akarizide und nematizideInfo
- Publication number
- DE2455680A1 DE2455680A1 DE19742455680 DE2455680A DE2455680A1 DE 2455680 A1 DE2455680 A1 DE 2455680A1 DE 19742455680 DE19742455680 DE 19742455680 DE 2455680 A DE2455680 A DE 2455680A DE 2455680 A1 DE2455680 A1 DE 2455680A1
- Authority
- DE
- Germany
- Prior art keywords
- iso
- active ingredient
- butyl
- spec
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
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- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241000883295 Symphyla Species 0.000 description 1
- 241000255588 Tephritidae Species 0.000 description 1
- 241001065719 Tetranychus ludeni Species 0.000 description 1
- 241000339374 Thrips tabaci Species 0.000 description 1
- 241001414989 Thysanoptera Species 0.000 description 1
- 241000511627 Tipula paludosa Species 0.000 description 1
- 241001238451 Tortrix viridana Species 0.000 description 1
- 241000018137 Trialeurodes vaporariorum Species 0.000 description 1
- 241001414833 Triatoma Species 0.000 description 1
- 241000254086 Tribolium <beetle> Species 0.000 description 1
- 241000255993 Trichoplusia ni Species 0.000 description 1
- 241000267823 Trogoderma Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 241000353223 Xenopsylla cheopis Species 0.000 description 1
- 241001466337 Yponomeuta Species 0.000 description 1
- 241001414985 Zygentoma Species 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 244000000054 animal parasite Species 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000018109 developmental process Effects 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
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical group CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 125000005059 halophenyl group Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 239000012074 organic phase 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
- 244000052769 pathogen Species 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 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
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4075—Esters with hydroxyalkyl compounds
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
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)
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742455680 DE2455680A1 (de) | 1974-11-25 | 1974-11-25 | Substituierte carboxylmethyl(di) thiol(thiono)-phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide, akarizide und nematizide |
| GB4310275A GB1478105A (en) | 1974-11-25 | 1975-10-21 | Carboxymethyl-di-thiol-thiono-phosphoric-phosphonic-acid exters and ester-amides and their use as insecticides acaricides and nematicides |
| JP50139381A JPS5175025A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-11-25 | 1975-11-21 | |
| AU86856/75A AU8685675A (en) | 1974-11-25 | 1975-11-21 | Carboxylmethyl%di<thiol%thiono<phosphoric-%phosphonic< acid esters and ester-amides and their use as insecticides, acar- icides and nematicides |
| DD189615A DD125711A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-11-25 | 1975-11-21 | |
| JP50139382A JPS5173132A (en) | 1974-11-25 | 1975-11-21 | Satsukonchu satsudani oyobi satsusenchuzai |
| ZA757339A ZA757339B (en) | 1974-11-25 | 1975-11-24 | Novel carboxylmethyl(di)thiol(thiono)phosphoric(phosphonic)acid esters and ester-amides and their use as insecticides,acaricides and nematicides |
| BR7507759*A BR7507759A (pt) | 1974-11-25 | 1975-11-24 | Processo para a preparacao de esteres ou esteramidas de acido carboxilmetil(di)tiol(tiono)-fosforico(fosfonico),substituidos,e composicoes inseticidas,acaricidas e nematocidas a base destes |
| IL48522A IL48522A0 (en) | 1974-11-25 | 1975-11-24 | Novel esters and ester-amides of carbalkoxymethylthiolphosphoric and-phosphonic acids and their sulfur analogues,their preparation and their use as insecticides,acaricides and nematocides |
| AT891275A AT334400B (de) | 1974-11-25 | 1975-11-24 | Verfahren zur herstellung von neuen, substituierten carboxylmethyl(di)thiol(thiono)-phosphor(phosphon)-saureestern bzw. -esteramiden |
| DK528775A DK528775A (da) | 1974-11-25 | 1975-11-24 | Substituerede carboxymethyl(di)thiol(thiono)phosphor(phosphon) -syreestere og -esteramider samt fremgangsmade til disses fremstilling og anvendelse |
| BE162117A BE835864A (fr) | 1974-11-25 | 1975-11-24 | Nouveaux esters et amides d'esters carbuxy-methyliques substitues d'acide (di)thiul(thiono)-phosphorique (phosphonique), leur procede de preparation et leur application comme insecticides, acaricides et nematicides |
| LU73855A LU73855A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-11-25 | 1975-11-24 | |
| FR7536037A FR2291982A1 (fr) | 1974-11-25 | 1975-11-25 | Nouveaux esters et amides d'esters carboxymethyliques substitues d'acide (di)thiol(thiono)-phosphorique (phosphonique), leur procede de preparation et leur application comme insecticides, acaricides et nematicides |
| NL7513745A NL7513745A (nl) | 1974-11-25 | 1975-11-25 | Werkwijze voor het bereiden van gesubstitueerde carboxymethyl(di)thiol(thiono)fosfor(fosfon)zuur- esters of -esteramiden, alsmede de toepassing daarvan als insecticiden, acariciden en nemato- ciden. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742455680 DE2455680A1 (de) | 1974-11-25 | 1974-11-25 | Substituierte carboxylmethyl(di) thiol(thiono)-phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide, akarizide und nematizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2455680A1 true DE2455680A1 (de) | 1976-05-26 |
Family
ID=5931658
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19742455680 Pending DE2455680A1 (de) | 1974-11-25 | 1974-11-25 | Substituierte carboxylmethyl(di) thiol(thiono)-phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide, akarizide und nematizide |
Country Status (14)
-
1974
- 1974-11-25 DE DE19742455680 patent/DE2455680A1/de active Pending
-
1975
- 1975-10-21 GB GB4310275A patent/GB1478105A/en not_active Expired
- 1975-11-21 JP JP50139381A patent/JPS5175025A/ja active Pending
- 1975-11-21 AU AU86856/75A patent/AU8685675A/en not_active Expired
- 1975-11-21 DD DD189615A patent/DD125711A5/xx unknown
- 1975-11-21 JP JP50139382A patent/JPS5173132A/ja active Pending
- 1975-11-24 AT AT891275A patent/AT334400B/de not_active IP Right Cessation
- 1975-11-24 BE BE162117A patent/BE835864A/xx unknown
- 1975-11-24 IL IL48522A patent/IL48522A0/xx unknown
- 1975-11-24 ZA ZA757339A patent/ZA757339B/xx unknown
- 1975-11-24 BR BR7507759*A patent/BR7507759A/pt unknown
- 1975-11-24 DK DK528775A patent/DK528775A/da unknown
- 1975-11-24 LU LU73855A patent/LU73855A1/xx unknown
- 1975-11-25 NL NL7513745A patent/NL7513745A/xx unknown
- 1975-11-25 FR FR7536037A patent/FR2291982A1/fr not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| ZA757339B (en) | 1976-11-24 |
| BR7507759A (pt) | 1976-08-10 |
| JPS5175025A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-06-29 |
| AU8685675A (en) | 1977-05-26 |
| FR2291982A1 (fr) | 1976-06-18 |
| DK528775A (da) | 1976-05-26 |
| AT334400B (de) | 1976-01-10 |
| GB1478105A (en) | 1977-06-29 |
| NL7513745A (nl) | 1976-05-28 |
| ATA891275A (de) | 1976-05-15 |
| IL48522A0 (en) | 1976-01-30 |
| BE835864A (fr) | 1976-05-24 |
| JPS5173132A (en) | 1976-06-24 |
| LU73855A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-09-06 |
| DD125711A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1977-05-11 |
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