CS195315B2 - Herbicides and method of preparing active substances therefor - Google Patents
Herbicides and method of preparing active substances therefor Download PDFInfo
- Publication number
- CS195315B2 CS195315B2 CS766763A CS676376A CS195315B2 CS 195315 B2 CS195315 B2 CS 195315B2 CS 766763 A CS766763 A CS 766763A CS 676376 A CS676376 A CS 676376A CS 195315 B2 CS195315 B2 CS 195315B2
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- Czechoslovakia
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- compounds
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- 238000000034 method Methods 0.000 title claims description 14
- 239000013543 active substance Substances 0.000 title description 7
- 239000004009 herbicide Substances 0.000 title description 6
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 5
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- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- 239000001301 oxygen Substances 0.000 claims abstract description 5
- 229910052717 sulfur Chemical group 0.000 claims abstract description 5
- 239000011593 sulfur Chemical group 0.000 claims abstract description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 4
- -1 3-methylpentamethylene group Chemical group 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 20
- 238000002360 preparation method Methods 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 6
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- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 3
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- 239000001257 hydrogen Substances 0.000 claims description 2
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- 244000038559 crop plants Species 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000004119 disulfanediyl group Chemical group *SS* 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 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
- QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical class ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
- 235000009529 zinc sulphate Nutrition 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
- C07F9/06—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
-
- 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
- C07F9/5532—Seven-(or more) membered rings
-
- 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
- C07F9/59—Hydrogenated 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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50126322A JPS5251028A (en) | 1975-10-22 | 1975-10-22 | Herbicide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS195315B2 true CS195315B2 (en) | 1980-01-31 |
Family
ID=14932306
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS766763A CS195315B2 (en) | 1975-10-22 | 1976-10-20 | Herbicides and method of preparing active substances therefor |
Country Status (24)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5194430A (en) * | 1990-05-17 | 1993-03-16 | Merrell Dow Pharmaceuticals Inc. | Heterocyclic-nmda antagonists |
| CN106810577B (zh) * | 2015-11-30 | 2018-08-07 | 浙江新安化工集团股份有限公司 | 一种含杂环草甘膦衍生物及其制备方法以及应用 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA710340A (en) * | 1965-05-25 | Monsanto Company | Phosphorothioates | |
| NL107782C (US20100056889A1-20100304-C00004.png) * | 1958-07-12 | |||
| US2959610A (en) * | 1959-01-23 | 1960-11-08 | American Cyanamid Co | Preparation of s-1-(nu-substituted carbamoyl) alkyl omicron, omicron-dialkyl phosphorodithioates |
| GB947778A (en) * | 1959-01-30 | 1964-01-29 | Fisons Pest Control Ltd | Improvements in or relating to the production of carbamylmethyl phosphorothioates |
| GB1052552A (US20100056889A1-20100304-C00004.png) * | 1963-05-13 | |||
| US3449109A (en) * | 1965-02-01 | 1969-06-10 | Velsicol Chemical Corp | Phosphorylated acetamides as herbicides |
| US3388122A (en) * | 1965-10-08 | 1968-06-11 | Stauffer Chemical Co | Certain nu-acyl-3-azabicyclo-(3. 2. 2) nonane compounds |
| US3385689A (en) * | 1965-10-11 | 1968-05-28 | Velsicol Chemical Corp | Method of controlling undesirable plant growth |
| US3833600A (en) * | 1968-12-10 | 1974-09-03 | Ciba Geigy Ag | Dithiophosphates |
| DE1812497C3 (de) * | 1967-12-13 | 1978-04-13 | Ciba-Geigy Ag, Basel (Schweiz) | N-Phosphinothioyl-thiomethyl-carbonyl-piperidine, Verfahren zu ihrer Herstellung und diese enthaltende Mittel |
| US3501461A (en) * | 1968-01-18 | 1970-03-17 | Allied Chem | Azabicyclic phosphonate |
| JPS5527882B1 (US20100056889A1-20100304-C00004.png) * | 1970-05-13 | 1980-07-24 | ||
| CH559506A5 (US20100056889A1-20100304-C00004.png) * | 1971-10-21 | 1975-03-14 | Ciba Geigy Ag | |
| US3955957A (en) * | 1972-01-20 | 1976-05-11 | Ciba-Geigy Corporation | Phosphoryl-acylamines for inhibiting plant growth |
| JPS5032309B2 (US20100056889A1-20100304-C00004.png) * | 1972-10-12 | 1975-10-20 | ||
| GB1436214A (en) * | 1972-08-05 | 1976-05-19 | Sumitomo Chemical Co | Amido containing phosphorothiolate pesticide |
| US3997526A (en) * | 1972-11-30 | 1976-12-14 | Sumitomo Chemical Company, Limited | Amido phosphorothiolate pesticide |
| IT988829B (it) * | 1973-05-30 | 1975-04-30 | Eigenmann Ludwig | Perfezionamento agli elementi irru videnti per materiali per segnale tica stradale orizzontale e segna lazioni stradali orizzontali com predenti tali elementi |
| DE2329044A1 (de) * | 1973-06-07 | 1975-01-02 | Basf Ag | Herbizid |
| JPS5213582B2 (US20100056889A1-20100304-C00004.png) * | 1973-07-25 | 1977-04-15 |
-
1975
- 1975-10-22 JP JP50126322A patent/JPS5251028A/ja active Granted
-
1976
- 1976-09-22 US US05/725,615 patent/US4132542A/en not_active Expired - Lifetime
- 1976-10-18 EG EG638/76A patent/EG12144A/xx active
- 1976-10-19 IL IL50715A patent/IL50715A0/xx unknown
- 1976-10-19 PT PT65731A patent/PT65731B/pt unknown
- 1976-10-20 GB GB43528/76A patent/GB1527173A/en not_active Expired
- 1976-10-20 PL PL1976193151A patent/PL99605B1/pl unknown
- 1976-10-20 AU AU18851/76A patent/AU510109B2/en not_active Expired
- 1976-10-20 BR BR7607018A patent/BR7607018A/pt unknown
- 1976-10-20 TR TR18942A patent/TR18942A/xx unknown
- 1976-10-20 NL NL7611602A patent/NL7611602A/xx not_active Application Discontinuation
- 1976-10-20 DD DD7600195371A patent/DD128336A5/xx unknown
- 1976-10-20 CS CS766763A patent/CS195315B2/cs unknown
- 1976-10-21 GR GR51989A patent/GR63122B/el unknown
- 1976-10-21 IE IE2316/76A patent/IE43805B1/en unknown
- 1976-10-21 ES ES452592A patent/ES452592A1/es not_active Expired
- 1976-10-21 DK DK475976AA patent/DK141203B/da unknown
- 1976-10-21 CA CA263,899A patent/CA1072551A/en not_active Expired
- 1976-10-21 DE DE19762647481 patent/DE2647481A1/de active Pending
- 1976-10-22 BE BE171706A patent/BE847539A/xx unknown
- 1976-10-22 FR FR7631945A patent/FR2328716A1/fr active Granted
- 1976-10-22 AT AT787876A patent/AT347740B/de not_active IP Right Cessation
- 1976-10-22 RO RO7688171A patent/RO69795A/ro unknown
- 1976-10-22 AR AR265195A patent/AR215604A1/es active
Also Published As
| Publication number | Publication date |
|---|---|
| BE847539A (fr) | 1977-04-22 |
| DK141203B (da) | 1980-02-04 |
| JPS5440611B2 (US20100056889A1-20100304-C00004.png) | 1979-12-04 |
| NL7611602A (nl) | 1977-04-26 |
| JPS5251028A (en) | 1977-04-23 |
| GB1527173A (en) | 1978-10-04 |
| TR18942A (tr) | 1977-12-20 |
| RO69795A (ro) | 1981-08-17 |
| FR2328716B1 (US20100056889A1-20100304-C00004.png) | 1980-06-13 |
| AR215604A1 (es) | 1979-10-31 |
| IE43805B1 (en) | 1981-06-03 |
| DE2647481A1 (de) | 1977-04-28 |
| BR7607018A (pt) | 1977-09-06 |
| IE43805L (en) | 1977-04-22 |
| DD128336A5 (de) | 1977-11-09 |
| ES452592A1 (es) | 1977-11-16 |
| ATA787876A (de) | 1978-05-15 |
| US4132542A (en) | 1979-01-02 |
| PT65731B (en) | 1978-04-18 |
| AU510109B2 (en) | 1980-06-05 |
| PL99605B1 (pl) | 1978-07-31 |
| FR2328716A1 (fr) | 1977-05-20 |
| GR63122B (en) | 1979-09-11 |
| IL50715A0 (en) | 1976-12-31 |
| DK141203C (US20100056889A1-20100304-C00004.png) | 1980-07-28 |
| PT65731A (en) | 1976-11-01 |
| DK475976A (US20100056889A1-20100304-C00004.png) | 1977-04-23 |
| AT347740B (de) | 1979-01-10 |
| AU1885176A (en) | 1978-04-27 |
| EG12144A (en) | 1978-09-30 |
| CA1072551A (en) | 1980-02-26 |
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