DE3013264A1 - 0-(2-nitro-5-(2-chlor-4-trifluormethyl-phenoxy)-phenyl)-(thiono)(thiol)-phosphor(phosphon)-saeure-derivate, verfahren zu deren herstellung sowie deren verwendung als herbizide und pflanzenwuchsregulatoren - Google Patents
0-(2-nitro-5-(2-chlor-4-trifluormethyl-phenoxy)-phenyl)-(thiono)(thiol)-phosphor(phosphon)-saeure-derivate, verfahren zu deren herstellung sowie deren verwendung als herbizide und pflanzenwuchsregulatorenInfo
- Publication number
- DE3013264A1 DE3013264A1 DE19803013264 DE3013264A DE3013264A1 DE 3013264 A1 DE3013264 A1 DE 3013264A1 DE 19803013264 DE19803013264 DE 19803013264 DE 3013264 A DE3013264 A DE 3013264A DE 3013264 A1 DE3013264 A1 DE 3013264A1
- Authority
- DE
- Germany
- Prior art keywords
- formula
- phenyl
- nitro
- chloro
- phosphorus
- 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.)
- Withdrawn
Links
- 239000004009 herbicide Substances 0.000 title claims abstract description 11
- 230000008635 plant growth Effects 0.000 title claims abstract description 7
- 229910052698 phosphorus Inorganic materials 0.000 title claims description 23
- 239000011574 phosphorus Substances 0.000 title claims description 23
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims description 15
- 230000002363 herbicidal effect Effects 0.000 title description 5
- 125000000962 organic group Chemical group 0.000 title 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 title 1
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 15
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 13
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 13
- 150000001768 cations Chemical class 0.000 claims abstract description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 5
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 5
- 238000007126 N-alkylation reaction Methods 0.000 claims abstract description 3
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 3
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 3
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract description 3
- -1 aluminum ion Chemical class 0.000 claims description 42
- 239000002253 acid Substances 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 37
- 241000196324 Embryophyta Species 0.000 claims description 25
- 150000003573 thiols Chemical class 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 239000000460 chlorine Chemical group 0.000 claims description 14
- 239000003085 diluting agent Substances 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 239000002585 base Substances 0.000 claims description 7
- 239000005648 plant growth regulator Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- WYTRKEWETULQOA-UHFFFAOYSA-N 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenol Chemical class C1=C([N+]([O-])=O)C(O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 WYTRKEWETULQOA-UHFFFAOYSA-N 0.000 claims description 6
- 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 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 229910001511 metal iodide Inorganic materials 0.000 claims description 6
- 125000001477 organic nitrogen group Chemical group 0.000 claims description 6
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- 239000011593 sulfur Chemical group 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
- 239000004606 Fillers/Extenders Substances 0.000 claims description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 229910001414 potassium ion Inorganic materials 0.000 claims description 3
- 230000001105 regulatory effect Effects 0.000 claims description 3
- 229910001415 sodium ion Inorganic materials 0.000 claims description 3
- 239000013543 active substance Substances 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 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 class 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 239000002837 defoliant Substances 0.000 abstract description 4
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- 239000003112 inhibitor Substances 0.000 abstract description 2
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 239000003139 biocide Substances 0.000 abstract 1
- 230000035784 germination Effects 0.000 abstract 1
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- 235000021317 phosphate Nutrition 0.000 abstract 1
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
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- 239000003995 emulsifying agent Substances 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 241000219146 Gossypium Species 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N Methyl ethyl ketone Natural products CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 4
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
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- 159000000000 sodium salts Chemical class 0.000 description 4
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- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 3
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- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
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- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
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- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
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- SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical class CC[N+](C)(CC)CC SEACXNRNJAXIBM-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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/242—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyaryl compounds
-
- 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
- A01N57/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34
- A01N57/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34 containing aromatic radicals
-
- 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
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/12—Esters of phosphoric acids with hydroxyaryl 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
- C07F9/18—Esters of thiophosphoric acids with hydroxyaryl 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
- C07F9/28—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)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19803013264 DE3013264A1 (de) | 1980-04-03 | 1980-04-03 | 0-(2-nitro-5-(2-chlor-4-trifluormethyl-phenoxy)-phenyl)-(thiono)(thiol)-phosphor(phosphon)-saeure-derivate, verfahren zu deren herstellung sowie deren verwendung als herbizide und pflanzenwuchsregulatoren |
| PT72720A PT72720B (en) | 1980-04-03 | 1981-03-24 | Process for the preparation of an herbicidal composition or of a plant growing regulation composition containing derivatives of the o-<2-nitro-5-(2-chloro-4-trifluoromethyl-phenoxi)-phenyl>-(thiono)(thiol)-phosphoric(phosphonic)acid |
| AU68833/81A AU6883381A (en) | 1980-04-03 | 1981-03-27 | 0-(2-nitro-5-(2-chloro-4-trifluoromethyl-phenoxy)-phenyl)- (thiono)-(thiol)-phosphoric(phosphonic) acid derivatives |
| IL62537A IL62537A0 (en) | 1980-04-03 | 1981-03-31 | Derivatives of 0-(2-nitro-5-(2-chloro-4-trifluoromethyl-phenoxy)-phenyl)-phosphoric and phosphonic acids and their mono-and dithio analogues,their preparation and their use as herbicides and plant growth regulators |
| JP4659481A JPS56152493A (en) | 1980-04-03 | 1981-03-31 | O.(2-nitro-5-(2-chloro-4-trifluoromethyl- phenoxy)-phenyl)-(thiono)(thiol)-phosphoric acid derivatives,their manufacture and their use for plant |
| GR64451A GR74815B (OSRAM) | 1980-04-03 | 1981-04-01 | |
| BR8102005A BR8102005A (pt) | 1980-04-03 | 1981-04-02 | Processo para a preparacao de derivados de acido 0-(2-nitro-5-(2-cloro-4-trifluormetil-fenoxi)-fenil-(tiono)-(tiol)-fosforico(fosfonico),composicoes herbicidas e reguladoras do crescimento de plantas,processo para o combate de ervas daninhas e para a preparacao de composicoes herbicidas |
| ZA00812203A ZA812203B (en) | 1980-04-03 | 1981-04-02 | O-(2-nitro-5-(2-chloro-4-grifluoro-methyl-phenoxy)-phenyl)-(thiono)(thiol)-phosporic(phosphonic)acid derivatives, processes for their preparation and their use as herbicides and plant growth regulators |
| DK150681A DK150681A (da) | 1980-04-03 | 1981-04-02 | O-(2-nitro-5-(2-chlor-4-trifluormethyl-phenoxy)-phenyl)-(thiono) (thiol)phosphor (phosphon)-syre-derivater deres fremstilling og anvendelse som herbicider og plantevaekstregulatorer |
| ES501053A ES501053A1 (es) | 1980-04-03 | 1981-04-03 | Procedimiento para la obtencion de derivados de acido o-(2- nitro-5-(2-cloro-4-trifluormetilfenoxi)-fenil)-(tiono)(tiol)-fosforico(fosfonico),de efecto herbicida y regulador del crecimiento de las plantas |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19803013264 DE3013264A1 (de) | 1980-04-03 | 1980-04-03 | 0-(2-nitro-5-(2-chlor-4-trifluormethyl-phenoxy)-phenyl)-(thiono)(thiol)-phosphor(phosphon)-saeure-derivate, verfahren zu deren herstellung sowie deren verwendung als herbizide und pflanzenwuchsregulatoren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3013264A1 true DE3013264A1 (de) | 1981-10-08 |
Family
ID=6099352
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19803013264 Withdrawn DE3013264A1 (de) | 1980-04-03 | 1980-04-03 | 0-(2-nitro-5-(2-chlor-4-trifluormethyl-phenoxy)-phenyl)-(thiono)(thiol)-phosphor(phosphon)-saeure-derivate, verfahren zu deren herstellung sowie deren verwendung als herbizide und pflanzenwuchsregulatoren |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS56152493A (OSRAM) |
| AU (1) | AU6883381A (OSRAM) |
| BR (1) | BR8102005A (OSRAM) |
| DE (1) | DE3013264A1 (OSRAM) |
| DK (1) | DK150681A (OSRAM) |
| ES (1) | ES501053A1 (OSRAM) |
| GR (1) | GR74815B (OSRAM) |
| IL (1) | IL62537A0 (OSRAM) |
| PT (1) | PT72720B (OSRAM) |
| ZA (1) | ZA812203B (OSRAM) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5514973B2 (ja) * | 2010-04-30 | 2014-06-04 | 独立行政法人産業技術総合研究所 | ホスホン酸ジエステル誘導体の製造方法 |
-
1980
- 1980-04-03 DE DE19803013264 patent/DE3013264A1/de not_active Withdrawn
-
1981
- 1981-03-24 PT PT72720A patent/PT72720B/pt unknown
- 1981-03-27 AU AU68833/81A patent/AU6883381A/en not_active Abandoned
- 1981-03-31 JP JP4659481A patent/JPS56152493A/ja active Pending
- 1981-03-31 IL IL62537A patent/IL62537A0/xx unknown
- 1981-04-01 GR GR64451A patent/GR74815B/el unknown
- 1981-04-02 BR BR8102005A patent/BR8102005A/pt unknown
- 1981-04-02 ZA ZA00812203A patent/ZA812203B/xx unknown
- 1981-04-02 DK DK150681A patent/DK150681A/da not_active IP Right Cessation
- 1981-04-03 ES ES501053A patent/ES501053A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AU6883381A (en) | 1981-10-08 |
| GR74815B (OSRAM) | 1984-07-12 |
| IL62537A0 (en) | 1981-05-20 |
| PT72720B (en) | 1982-03-24 |
| ES501053A1 (es) | 1982-01-16 |
| DK150681A (da) | 1981-10-04 |
| PT72720A (en) | 1981-04-01 |
| JPS56152493A (en) | 1981-11-26 |
| BR8102005A (pt) | 1981-10-06 |
| ZA812203B (en) | 1982-04-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8130 | Withdrawal |