BE544659A - - Google Patents
Info
- Publication number
- BE544659A BE544659A BE544659DA BE544659A BE 544659 A BE544659 A BE 544659A BE 544659D A BE544659D A BE 544659DA BE 544659 A BE544659 A BE 544659A
- Authority
- BE
- Belgium
- Prior art keywords
- methyl
- phenyl
- dithiophosphoric
- diethyl
- esters
- Prior art date
Links
- 150000002148 esters Chemical class 0.000 claims description 16
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 claims description 11
- 241000238631 Hexapoda Species 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 4
- 125000000746 allylic group Chemical group 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 125000006267 biphenyl group Chemical group 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 230000000749 insecticidal effect Effects 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000000686 essence Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 238000003756 stirring Methods 0.000 description 14
- -1 ester radicals Chemical class 0.000 description 13
- 239000002904 solvent Substances 0.000 description 13
- 229910052700 potassium Inorganic materials 0.000 description 12
- 239000001103 potassium chloride Substances 0.000 description 12
- 235000011164 potassium chloride Nutrition 0.000 description 12
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 11
- 238000004821 distillation Methods 0.000 description 11
- 239000011591 potassium Substances 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 241001124076 Aphididae Species 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 241000607479 Yersinia pestis Species 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- 239000012230 colorless oil Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 235000013601 eggs Nutrition 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 241000255925 Diptera Species 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241000238876 Acari Species 0.000 description 3
- 241000254171 Curculionidae Species 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- NEZGPRYOJVPJKL-UHFFFAOYSA-N 1-methylsulfanyl-4-nitrobenzene Chemical compound CSC1=CC=C([N+]([O-])=O)C=C1 NEZGPRYOJVPJKL-UHFFFAOYSA-N 0.000 description 2
- 241001674044 Blattodea Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 241000488583 Panonychus ulmi Species 0.000 description 2
- 241000254179 Sitophilus granarius Species 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000037406 food intake Effects 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000002895 organic esters Chemical class 0.000 description 2
- 230000003151 ovacidal effect Effects 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- DSMBOFNGRWWAJQ-UHFFFAOYSA-N 1,2-dichloro-4-(3,4-dichloro-2-methylphenyl)sulfanyl-3-methylbenzene Chemical compound C1=CC(Cl)=C(Cl)C(C)=C1SC1=CC=C(Cl)C(Cl)=C1C DSMBOFNGRWWAJQ-UHFFFAOYSA-N 0.000 description 1
- IHLDFHCSSCVPQW-UHFFFAOYSA-N 1-chloro-2-methylsulfanylbenzene Chemical compound CSC1=CC=CC=C1Cl IHLDFHCSSCVPQW-UHFFFAOYSA-N 0.000 description 1
- UQZPGHOJMQTOHB-UHFFFAOYSA-N 2-chloro-n-(2-chloroethyl)-n-ethylethanamine Chemical compound ClCCN(CC)CCCl UQZPGHOJMQTOHB-UHFFFAOYSA-N 0.000 description 1
- 241000254032 Acrididae Species 0.000 description 1
- 241000238421 Arthropoda Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000723353 Chrysanthemum Species 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- CZGGKXNYNPJFAX-UHFFFAOYSA-N Dimethyldithiophosphate Chemical compound COP(S)(=S)OC CZGGKXNYNPJFAX-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 240000001307 Myosotis scorpioides Species 0.000 description 1
- 241000118205 Ovicides Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241001450657 Parthenolecanium corni Species 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241001474791 Proboscis Species 0.000 description 1
- 241000198945 Prunus domestica subsp. syriaca Species 0.000 description 1
- 241001350474 Rhopalosiphum nymphaeae Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
- 241000135799 Thorius Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012072 active phase Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000007265 chloromethylation reaction Methods 0.000 description 1
- 239000004927 clay 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
- 230000006378 damage Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000002257 embryonic structure Anatomy 0.000 description 1
- 229940084434 fungoid Drugs 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000012073 inactive phase Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- HNKJADCVZUBCPG-UHFFFAOYSA-N thioanisole Chemical compound CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- OFLNOEMLSXBOFY-UHFFFAOYSA-K trisodium;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([S-])=S OFLNOEMLSXBOFY-UHFFFAOYSA-K 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009736 wetting Methods 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
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)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE544659A true BE544659A (da) |
Family
ID=172559
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE544659D BE544659A (da) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE544659A (da) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3179278A (en) * | 1963-07-01 | 1965-04-20 | Cohen William | Telescopic form containers and dispensers |
| US3246052A (en) * | 1962-12-26 | 1966-04-12 | Universal Oil Prod Co | Halogenated aromatic phosphate esters |
| US3274299A (en) * | 1963-05-17 | 1966-09-20 | Stauffer Chemical Co | O, o-dialkyl nitrophenoxymethyl-phosphorothioates |
-
0
- BE BE544659D patent/BE544659A/fr unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3246052A (en) * | 1962-12-26 | 1966-04-12 | Universal Oil Prod Co | Halogenated aromatic phosphate esters |
| US3274299A (en) * | 1963-05-17 | 1966-09-20 | Stauffer Chemical Co | O, o-dialkyl nitrophenoxymethyl-phosphorothioates |
| US3179278A (en) * | 1963-07-01 | 1965-04-20 | Cohen William | Telescopic form containers and dispensers |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR2597472A1 (fr) | Composes difluorohalogenomethoxyphenyle et compositions acaricides les contenant. | |
| CA1325013C (fr) | Esters d'acides cyclopropanecarboxyliques apparentes a l'acide pyrethrique, leur procede de preparation et leur application a la lutte contre les parasites | |
| CH618966A5 (da) | ||
| CH619689A5 (da) | ||
| EP0018894B1 (fr) | Esters de dérivés de l'alléthrolone et d'acides carboxyliques, leur procédé de préparation et les compositions les renfermant | |
| BE544659A (da) | ||
| BE882335A (fr) | Isomere geometrique de 1-triazolyl-styrenes substitues en poisition 1, leur preparation et leur utilisation comme fongicides, herbicides et/ou regulateurs de la croissance des plantes | |
| CA1248117A (fr) | Derives de l'acide cyclopropane carboxylique, leur preparation, et leur application a la lutte contre les parasites | |
| CH616314A5 (da) | ||
| FR2465417A1 (fr) | Produit et composition acaricides et procede de destruction des tiques et des acariens | |
| LU86096A1 (fr) | Nouveaux n-alkyl(ene)-n-(0,odisubstitue-thiophosphoryl)-n',n'-disubstitue-glycines amides,procede pour leur preparation et acaricide,insecticide et fongicide contenant ces composes comme substance active | |
| BE1000110A4 (fr) | Nouveaux derives d'esters d'acide carbamique, compositions pesticides les contenant et procede pour les preparer. | |
| CH629765A5 (fr) | Bis-carbamoyloximino disulfures n-substitues symetriques pesticides. | |
| EP0034556B1 (fr) | Compositions régulatrices de la croissance des plantes contenant comme matière active des dérivés de l'acide méthylène-2 succinamique et nouveaux dérivés de cet acide utilisables dans ces compositions | |
| JP2557456B2 (ja) | ５、９ージメチルペンタデカンおよび５、９ージメチルヘキサデカン | |
| CA1056384A (fr) | Derives thiazoliques organophosphores, procede de preparation | |
| EP0007255A1 (fr) | Esters d'acides cyclopropane carboxyliques substitués d'alcool alpha-cyané, leur procédé de préparation, les compositions pesticides les renfermant ainsi que leur application à titre de médicaments à usage vétérinaire | |
| BE826376A (fr) | Dinitroanilines | |
| BE833082R (fr) | Nouveaux esters phosphoriques de la pyrimidine utilisables comme produits pesticides et leur preparation | |
| CH506564A (fr) | Procédé de préparation de nouveaux amidoesters phosphorés de 2-alkoximino-2-alkoxy-éthyle | |
| BE888179A (fr) | Phenoxyphenylisothiourees, procede pour leur preparation et leur application dans la lutte antiparasitaire ainsi que phenoxyphenylthiourees comme produits intermediaires pour la preparation des phenoxyphenyliqothiourees ainsi que leur application dans la lutte antiparatitaire | |
| BE807131A (fr) | Nouveaux esters | |
| BE674102A (da) | ||
| KR800000250B1 (ko) | 유기포스포로티올레이트류의 제조방법 | |
| FR2477549A1 (fr) | Esters xanthenone-yliques d'acides phosphoriques et phosphoniques et leur utilisation dans des compositions insecticides |