DE2260576A1 - Phosphorsaeureimidat-derivate und dieselben enthaltende pestizide - Google Patents
Phosphorsaeureimidat-derivate und dieselben enthaltende pestizideInfo
- Publication number
- DE2260576A1 DE2260576A1 DE2260576A DE2260576A DE2260576A1 DE 2260576 A1 DE2260576 A1 DE 2260576A1 DE 2260576 A DE2260576 A DE 2260576A DE 2260576 A DE2260576 A DE 2260576A DE 2260576 A1 DE2260576 A1 DE 2260576A1
- Authority
- DE
- Germany
- Prior art keywords
- compound according
- och
- sch
- carbon atoms
- radical
- 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
- 239000000575 pesticide Substances 0.000 title claims description 4
- -1 PHOSPHORIC ACID IMIDATE DERIVATIVES Chemical class 0.000 title description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 title description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000002917 insecticide Substances 0.000 claims description 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 239000000642 acaricide Substances 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 230000001476 alcoholic effect Effects 0.000 description 5
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 5
- 241000238657 Blattella germanica Species 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 239000003053 toxin Substances 0.000 description 4
- 231100000765 toxin Toxicity 0.000 description 4
- 239000004744 fabric Substances 0.000 description 3
- 241001425390 Aphis fabae Species 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 2
- 241000567412 Estigmene acrea Species 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- 235000005291 Rumex acetosa Nutrition 0.000 description 2
- 240000007001 Rumex acetosella Species 0.000 description 2
- 241000256247 Spodoptera exigua Species 0.000 description 2
- 235000003513 sheep sorrel Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- NDQXKKFRNOPRDW-UHFFFAOYSA-N 1,1,1-triethoxyethane Chemical compound CCOC(C)(OCC)OCC NDQXKKFRNOPRDW-UHFFFAOYSA-N 0.000 description 1
- 244000106835 Bindesalat Species 0.000 description 1
- 235000000318 Bindesalat Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- STECJAGHUSJQJN-USLFZFAMSA-N LSM-4015 Chemical compound C1([C@@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-USLFZFAMSA-N 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 240000005407 Nasturtium officinale Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 240000007113 Rumex obtusifolius Species 0.000 description 1
- 235000009422 Rumex obtusifolius Nutrition 0.000 description 1
- 240000001260 Tropaeolum majus Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical compound Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 150000002905 orthoesters Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-L phosphoramidate Chemical compound NP([O-])([O-])=O PTMHPRAIXMAOOB-UHFFFAOYSA-L 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2458—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic of aliphatic amines
-
- 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)]
- C07F9/44—Amides thereof
- C07F9/4461—Amides thereof the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4465—Amides thereof the amide moiety containing a substituent or a structure which is considered as characteristic of aliphatic amines
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 |
|---|---|---|---|
| US20758771A | 1971-12-13 | 1971-12-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2260576A1 true DE2260576A1 (de) | 1973-06-20 |
Family
ID=22771193
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2260576A Pending DE2260576A1 (de) | 1971-12-13 | 1972-12-11 | Phosphorsaeureimidat-derivate und dieselben enthaltende pestizide |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS4867437A (xx) |
| AR (1) | AR195689A1 (xx) |
| AU (1) | AU4978972A (xx) |
| BE (1) | BE792671A (xx) |
| BR (1) | BR7208794D0 (xx) |
| DE (1) | DE2260576A1 (xx) |
| FR (1) | FR2163543B1 (xx) |
| GB (1) | GB1373893A (xx) |
| IL (1) | IL41113A0 (xx) |
| IT (1) | IT971803B (xx) |
| NL (1) | NL7216916A (xx) |
| ZA (1) | ZA728802B (xx) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0204949A1 (de) * | 1985-05-14 | 1986-12-17 | Nihon Tokushu Noyaku Seizo K.K. | Phosphoroimidate |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01233202A (ja) * | 1988-03-11 | 1989-09-19 | Sumitomo Chem Co Ltd | チオリン酸エステルの安定化方法およびそれを有効成分とする安定な農薬組成物 |
-
0
- BE BE792671D patent/BE792671A/xx unknown
-
1972
- 1972-12-07 AU AU49789/72A patent/AU4978972A/en not_active Expired
- 1972-12-11 DE DE2260576A patent/DE2260576A1/de active Pending
- 1972-12-12 FR FR7244224A patent/FR2163543B1/fr not_active Expired
- 1972-12-12 AR AR245593A patent/AR195689A1/es active
- 1972-12-12 GB GB5688472A patent/GB1373893A/en not_active Expired
- 1972-12-13 JP JP47124441A patent/JPS4867437A/ja active Pending
- 1972-12-13 IT IT32834/72A patent/IT971803B/it active
- 1972-12-13 ZA ZA728802A patent/ZA728802B/xx unknown
- 1972-12-13 BR BR008794/72A patent/BR7208794D0/pt unknown
- 1972-12-13 NL NL7216916A patent/NL7216916A/xx unknown
- 1972-12-18 IL IL41113A patent/IL41113A0/xx unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0204949A1 (de) * | 1985-05-14 | 1986-12-17 | Nihon Tokushu Noyaku Seizo K.K. | Phosphoroimidate |
| US4692436A (en) * | 1985-05-14 | 1987-09-08 | Nihon Tokushu Noyaku Seizo K.K. | Phosphoroimidates as pesticides |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2163543A1 (xx) | 1973-07-27 |
| GB1373893A (en) | 1974-11-13 |
| IL41113A0 (en) | 1973-02-28 |
| BR7208794D0 (pt) | 1973-08-30 |
| BE792671A (fr) | 1973-06-13 |
| AR195689A1 (es) | 1973-10-31 |
| ZA728802B (en) | 1973-09-26 |
| AU4978972A (en) | 1974-06-13 |
| IT971803B (it) | 1974-05-10 |
| JPS4867437A (xx) | 1973-09-14 |
| FR2163543B1 (xx) | 1976-08-20 |
| NL7216916A (xx) | 1973-06-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2052379B2 (de) | 0-(N-Alkoxy-benzimidoylHthiono)phosphor(phosphon)säureester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Insektizide und Akarizide | |
| EP0100528A2 (de) | Neue (Di)-thiophosphor- und -phosphonsäure-Derivate, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung im Pflanzenschutz | |
| DE2462422A1 (de) | 2-carbamoyloximino-1,4-oxathiacyclohexane sowie deren 4-oxide und 4,4-dioxide und verfahren zu deren herstellung | |
| DE2260576A1 (de) | Phosphorsaeureimidat-derivate und dieselben enthaltende pestizide | |
| DE2732930C2 (de) | Neue 0-Äthyl-S-n-propyl-O-2,2,2- trihalogenäthylphosphorthiolate (oder -thionothiolate), Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide | |
| DE3118257A1 (de) | Pestizide s(-1.2.4-triazol-5-ylmethyl)-(di)-thiophosph(on)ate und verfahren zu ihrer herstellung | |
| DE2163392C3 (de) | Neue Phosphorsäureester sowie Verfahren zu deren Herstellung | |
| US4194029A (en) | Novel 4-chromanone-7-phosphates and phosphonates and the insecticidal use thereof | |
| DE2232076A1 (de) | Organische phosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide bzw. nematozide | |
| DE1768399A1 (de) | O-Alkyl-O-aryl-thiolphosphorsaeureester | |
| DE2246759A1 (de) | Neue substituierte trithiophosphonate und ihre verwendung als insektizide | |
| US3947481A (en) | Organotin miticidal and insecticidal compounds | |
| CH627620A5 (en) | Method and composition for controlling insects and acarids | |
| US3642958A (en) | Isobutoxy-s-(4-chlorophenyl) ethylphosphonodithioate | |
| US4036958A (en) | Insecticidal and miticidal active isothiuronium tricyclohexyl tin imide | |
| US3737532A (en) | Insecticidal isobutoxy ethylphosphonodithioate esters | |
| DE2034478C3 (de) | O-Alkyl-O-Phenyl-S-Alkoxyäthylphosphorthiolate mit insektizider und fungizider Wirkung | |
| US3351680A (en) | Omicron, omicron-diloweralkyl phosphorodithioyl-methyl-substituted mercaptoacetates | |
| DE2243612A1 (de) | Thiophen-glyoxylonitril-oxim-phosphorsaeurederivate und ihre verwendung | |
| DE1935758C (de) | (Thio) Phosphonsaureester und ihre Verwendung als Wirkstoffe in Schädlings bekampfungsmitteln | |
| AT362197B (de) | Verfahren zur bekaempfung von insekten, milben und nematoden | |
| CH532083A (de) | Verfahren zur Herstellung von neuen Amidothionophosphorsäurephenylestern, sowie ihre Verwendung zur Herstellung von insektiziden und akariziden Mitteln | |
| DE1668047C (de) | Amidothionophosphorsäurephenylester, deren Herstellung sowie insektizide und akarizide Mittel | |
| US4044025A (en) | Organotin miticidal and insecticidal compounds | |
| DE1668012C3 (de) | Verfahren zur Herstellung von Thiol- bzw. Thionothiolphosphor-(on) -säureestern, Thionothiolphosphor-(on)-säureester und diese enthaltende insektizide, akarizide und nematozide Mittel |