DD144710A5 - Herbizide zusammensetzung - Google Patents
Herbizide zusammensetzung Download PDFInfo
- Publication number
- DD144710A5 DD144710A5 DD79214208A DD21420879A DD144710A5 DD 144710 A5 DD144710 A5 DD 144710A5 DD 79214208 A DD79214208 A DD 79214208A DD 21420879 A DD21420879 A DD 21420879A DD 144710 A5 DD144710 A5 DD 144710A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- trifluoroacetyl
- glycinate
- ethyl
- group
- mol
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 31
- 230000002363 herbicidal effect Effects 0.000 title claims description 21
- -1 benzylthio, phenylthio Chemical group 0.000 claims description 54
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 claims description 42
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 7
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 5
- 125000005108 alkenylthio group Chemical group 0.000 claims description 5
- 125000004414 alkyl thio group Chemical group 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- ZERULLAPCVRMCO-UHFFFAOYSA-N Dipropyl sulfide Chemical group CCCSCCC ZERULLAPCVRMCO-UHFFFAOYSA-N 0.000 claims 1
- BESRQCXTEGIJKV-UHFFFAOYSA-N [[2-(2,5-dichlorophenyl)sulfanyloxy-2-oxoethyl]amino]methylphosphonic acid Chemical compound P(=O)(O)(O)CNCC(=O)OSC1=C(C=CC(=C1)Cl)Cl BESRQCXTEGIJKV-UHFFFAOYSA-N 0.000 claims 1
- 239000001963 growth medium Substances 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 121
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 72
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- 241000196324 Embryophyta Species 0.000 description 21
- 239000000706 filtrate Substances 0.000 description 21
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 20
- 239000003208 petroleum Substances 0.000 description 15
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- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 6
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- 239000004009 herbicide Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
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- 230000008018 melting Effects 0.000 description 4
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 4
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 description 3
- 244000062793 Sorghum vulgare Species 0.000 description 3
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- 229910052708 sodium Inorganic materials 0.000 description 3
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- MKJBZNABCZRVPC-UHFFFAOYSA-N 2-[phosphonomethyl-(2,2,2-trifluoroacetyl)amino]acetic acid Chemical class OC(=O)CN(CP(O)(O)=O)C(=O)C(F)(F)F MKJBZNABCZRVPC-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- LOCHFZBWPCLPAN-UHFFFAOYSA-N butane-2-thiol Chemical compound CCC(C)S LOCHFZBWPCLPAN-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 2
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- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 230000002262 irrigation Effects 0.000 description 2
- 238000003973 irrigation Methods 0.000 description 2
- CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical compound OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 2
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 2
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- TXFJNXUNTJSKDD-UHFFFAOYSA-N 2-methoxyethyl 2-[dichlorooxyphosphorylmethyl-(2,2,2-trifluoroacetyl)amino]acetate Chemical compound COCCOC(=O)CN(C(=O)C(F)(F)F)CP(=O)(OCl)OCl TXFJNXUNTJSKDD-UHFFFAOYSA-N 0.000 description 1
- BDFAOUQQXJIZDG-UHFFFAOYSA-N 2-methylpropane-1-thiol Chemical compound CC(C)CS BDFAOUQQXJIZDG-UHFFFAOYSA-N 0.000 description 1
- WRXOZRLZDJAYDR-UHFFFAOYSA-N 3-methylbenzenethiol Chemical compound CC1=CC=CC(S)=C1 WRXOZRLZDJAYDR-UHFFFAOYSA-N 0.000 description 1
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- XDCIZODHDDBBJZ-UHFFFAOYSA-N [dichloro-[(2-ethoxy-2-oxoethyl)-(2,2,2-trifluoroacetyl)amino]methyl]phosphonic acid Chemical compound CCOC(=O)CN(C(=O)C(F)(F)F)C(Cl)(Cl)P(O)(O)=O XDCIZODHDDBBJZ-UHFFFAOYSA-N 0.000 description 1
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- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-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
- C07F9/28—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
- C07F9/4087—Esters with arylalkanols
-
- 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
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
-
- 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
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- 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
- C07F9/4078—Esters with unsaturated acyclic alcohols
-
- 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
- C07F9/4084—Esters with hydroxyaryl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (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 |
|---|---|---|---|
| US05/922,900 US4175946A (en) | 1978-07-10 | 1978-07-10 | Thio derivatives of N-trifluoroacetyl-N-phosphonomethylglycine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD144710A5 true DD144710A5 (de) | 1980-11-05 |
Family
ID=25447743
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79214208A DD144710A5 (de) | 1978-07-10 | 1979-07-09 | Herbizide zusammensetzung |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4175946A (ro) |
| EP (1) | EP0008158B1 (ro) |
| JP (1) | JPS5513291A (ro) |
| AR (1) | AR224129A1 (ro) |
| AU (1) | AU519676B2 (ro) |
| BG (1) | BG33434A3 (ro) |
| BR (1) | BR7904338A (ro) |
| CA (1) | CA1131653A (ro) |
| CS (1) | CS208119B2 (ro) |
| DD (1) | DD144710A5 (ro) |
| DE (1) | DE2961546D1 (ro) |
| DK (1) | DK148024C (ro) |
| HU (1) | HU185773B (ro) |
| IL (1) | IL57747A (ro) |
| PH (1) | PH16319A (ro) |
| PL (1) | PL117081B1 (ro) |
| RO (2) | RO83701B (ro) |
| SU (1) | SU1347860A3 (ro) |
| ZA (1) | ZA793414B (ro) |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL124981C (ro) * | 1962-12-27 | 1900-01-01 | ||
| US3894125A (en) * | 1970-09-28 | 1975-07-08 | Ciba Geigy Ag | Phosphonic acid dithiol esters |
| US3799758A (en) * | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
| PH16509A (en) * | 1971-03-10 | 1983-11-08 | Monsanto Co | N-phosphonomethylglycine phytotoxicant composition |
| US3853530A (en) * | 1971-03-10 | 1974-12-10 | Monsanto Co | Regulating plants with n-phosphonomethylglycine and derivatives thereof |
| US3948975A (en) * | 1974-08-05 | 1976-04-06 | Monsanto Company | Hydroxyalkyl esters of N-phosphonomethyl glycine |
| US4042370A (en) * | 1974-09-18 | 1977-08-16 | Sandoz Ltd. | Di-(acyloxyalkyl)-β-haloethane-phosphonates and dithiophosphonates and use as plant growth regulators |
| US3970695A (en) * | 1975-05-23 | 1976-07-20 | Monsanto Company | N-(perfluoroacyl)-N-phosphonomethyl glycine compounds, method of preparing same |
| US3991095A (en) * | 1975-12-29 | 1976-11-09 | Monsanto Company | N-thiolcarbonyl derivatives of N-phosphonomethylglycine |
| MX3898E (es) * | 1975-12-29 | 1981-09-10 | Monsanto Co | Procedimiento mejorado para la preparacion de triesteres de n-fosfonometilglicina |
-
1978
- 1978-07-10 US US05/922,900 patent/US4175946A/en not_active Expired - Lifetime
-
1979
- 1979-06-06 AR AR277210A patent/AR224129A1/es active
- 1979-07-06 DE DE7979301305T patent/DE2961546D1/de not_active Expired
- 1979-07-06 EP EP79301305A patent/EP0008158B1/en not_active Expired
- 1979-07-09 JP JP8737679A patent/JPS5513291A/ja active Granted
- 1979-07-09 SU SU792790354A patent/SU1347860A3/ru active
- 1979-07-09 PL PL1979216977A patent/PL117081B1/pl unknown
- 1979-07-09 DK DK287379A patent/DK148024C/da not_active IP Right Cessation
- 1979-07-09 ZA ZA793414A patent/ZA793414B/xx unknown
- 1979-07-09 IL IL57747A patent/IL57747A/xx unknown
- 1979-07-09 CS CS794811A patent/CS208119B2/cs unknown
- 1979-07-09 DD DD79214208A patent/DD144710A5/de unknown
- 1979-07-09 BR BR7904338A patent/BR7904338A/pt unknown
- 1979-07-09 PH PH22749A patent/PH16319A/en unknown
- 1979-07-09 HU HU79MO1055A patent/HU185773B/hu unknown
- 1979-07-09 AU AU48778/79A patent/AU519676B2/en not_active Ceased
- 1979-07-09 RO RO105992A patent/RO83701B/ro unknown
- 1979-07-09 RO RO7998096A patent/RO78768A/ro unknown
- 1979-07-09 BG BG044251A patent/BG33434A3/xx unknown
- 1979-07-09 CA CA331,412A patent/CA1131653A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BR7904338A (pt) | 1980-04-08 |
| IL57747A0 (en) | 1979-11-30 |
| RO83701A (ro) | 1984-03-15 |
| ZA793414B (en) | 1980-07-30 |
| DK148024B (da) | 1985-02-04 |
| JPS5513291A (en) | 1980-01-30 |
| EP0008158A1 (en) | 1980-02-20 |
| HU185773B (en) | 1985-03-28 |
| RO78768A (ro) | 1982-04-12 |
| PL216977A1 (ro) | 1980-05-05 |
| EP0008158B1 (en) | 1981-12-09 |
| CA1131653A (en) | 1982-09-14 |
| AU519676B2 (en) | 1981-12-17 |
| PL117081B1 (en) | 1981-07-31 |
| DK148024C (da) | 1985-07-08 |
| US4175946A (en) | 1979-11-27 |
| RO83701B (ro) | 1984-03-30 |
| PH16319A (en) | 1983-09-05 |
| DK287379A (da) | 1980-01-11 |
| AU4877879A (en) | 1980-01-17 |
| DE2961546D1 (en) | 1982-02-04 |
| IL57747A (en) | 1982-08-31 |
| SU1347860A3 (ru) | 1987-10-23 |
| AR224129A1 (es) | 1981-10-30 |
| CS208119B2 (en) | 1981-08-31 |
| JPS5735920B2 (ro) | 1982-07-31 |
| BG33434A3 (en) | 1983-02-15 |
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