DE1298531B - Verfahren zur Herstellung von Organozinnkomplexen - Google Patents
Verfahren zur Herstellung von OrganozinnkomplexenInfo
- Publication number
- DE1298531B DE1298531B DEB83585A DEB0083585A DE1298531B DE 1298531 B DE1298531 B DE 1298531B DE B83585 A DEB83585 A DE B83585A DE B0083585 A DEB0083585 A DE B0083585A DE 1298531 B DE1298531 B DE 1298531B
- Authority
- DE
- Germany
- Prior art keywords
- group
- halogen
- optionally
- substituted
- mono
- 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
- 238000000034 method Methods 0.000 title claims 4
- 239000000460 chlorine Substances 0.000 claims description 28
- 229910052736 halogen Chemical group 0.000 claims description 22
- 150000002367 halogens Chemical group 0.000 claims description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- PRPNZPPJPIEXJI-UHFFFAOYSA-N 2h-triazin-1-amine Chemical group NN1NN=CC=C1 PRPNZPPJPIEXJI-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 4
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 4
- 125000001769 aryl amino group Chemical group 0.000 claims description 4
- 150000005840 aryl radicals Chemical class 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 4
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 125000004437 phosphorous atom Chemical group 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 125000004149 thio group Chemical group *S* 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 125000001691 aryl alkyl amino group Chemical group 0.000 claims description 3
- 125000005110 aryl thio group Chemical group 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910021626 Tin(II) chloride Inorganic materials 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Chemical group 0.000 claims description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 150000003016 phosphoric acids Chemical class 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- CPKHPYQIXCUKQJ-UHFFFAOYSA-N 1-di(piperidin-1-yl)phosphorylpiperidine Chemical compound C1CCCCN1P(N1CCCCC1)(=O)N1CCCCC1 CPKHPYQIXCUKQJ-UHFFFAOYSA-N 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- 241000238008 Cerithidea rhizophorarum Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000005791 algae growth Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- VEULIWWJVLYNEX-UHFFFAOYSA-N n-[dimethylamino(phenoxy)phosphoryl]-n-methylmethanamine Chemical compound CN(C)P(=O)(N(C)C)OC1=CC=CC=C1 VEULIWWJVLYNEX-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/6533—Six-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
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
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)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL131206D NL131206C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1965-09-03 | ||
| DEB83585A DE1298531B (de) | 1965-09-03 | 1965-09-03 | Verfahren zur Herstellung von Organozinnkomplexen |
| CH1232466A CH490421A (de) | 1965-09-03 | 1966-08-25 | Verfahren zur Herstellung von neuen Zinnkomplexverbindungen und deren Verwendung als Schädlingsbekämpfungsmittel |
| ES0330802A ES330802A1 (es) | 1965-09-03 | 1966-08-31 | Procedimiento para la preparacion de nuevos compuestos complejos de estaño. |
| NL6612312A NL6612312A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1965-09-03 | 1966-08-31 | |
| IL26433A IL26433A (en) | 1965-09-03 | 1966-08-31 | Oregano complex compounds - tin that are the result of phosphoric acid and their preparation |
| AT01444/67A AT284542B (de) | 1965-09-03 | 1966-09-01 | Schaedlingsbekaempfungsmittel |
| BE686314D BE686314A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1965-09-03 | 1966-09-01 | |
| GB39418/66A GB1160693A (en) | 1965-09-03 | 1966-09-02 | Organotin Compounds derived from Phosporic Acid |
| FR75149A FR1495647A (fr) | 1965-09-03 | 1966-09-02 | Procédé pour la fabrication de nouveaux composés complexes d'étain |
| BR182588/66A BR6682588D0 (pt) | 1965-09-03 | 1966-09-02 | Processo para a obtencao e aplicacao de novos compostos complexos de estanho e composicoes praguicidas baseadas nos mesmos |
| US577197A US3502690A (en) | 1965-09-03 | 1966-09-06 | (bis - dimethylamino)-(3 - phenyl - 5 - amino-1,2,4-triazolo) - phosphineoxide triphenyl-chlorostannate |
| ES340546A ES340546A1 (es) | 1965-09-03 | 1967-05-13 | Procedimiento de empleo como insecticidas de nuevos com- puestos complejos de estano. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB83585A DE1298531B (de) | 1965-09-03 | 1965-09-03 | Verfahren zur Herstellung von Organozinnkomplexen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1298531B true DE1298531B (de) | 1969-07-03 |
Family
ID=6982043
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEB83585A Pending DE1298531B (de) | 1965-09-03 | 1965-09-03 | Verfahren zur Herstellung von Organozinnkomplexen |
Country Status (10)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3947461A (en) * | 1972-10-19 | 1976-03-30 | Stauffer Chemical Company | Organotin miticidal and insecticidal compounds |
| US3947565A (en) * | 1973-08-01 | 1976-03-30 | Smithkline Corporation | Anti-arthritic compositions comprising s-heterocyclic derivatives of phosphine or phosphite gold mercaptides and methods of producing anti-arthritic activity |
| US3883546A (en) * | 1973-08-01 | 1975-05-13 | Smithkline Corp | S-heterocyclic derivatives of phosphine or phosphite gold mercaptides |
| US4018800A (en) * | 1975-05-06 | 1977-04-19 | Stauffer Chemical Company | Organotin miticidal and insecticidal compounds |
| US4554367A (en) * | 1982-10-06 | 1985-11-19 | Ciga-Geigy Corporation | Phosphonium organohalogenostannates-IV |
| EP3053928A4 (en) * | 2013-10-01 | 2017-03-01 | Adeka Corporation | Phosphorus-containing compound, and curable epoxy resin composition containing same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1052529A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1963-03-25 |
-
0
- NL NL131206D patent/NL131206C/xx active
-
1965
- 1965-09-03 DE DEB83585A patent/DE1298531B/de active Pending
-
1966
- 1966-08-25 CH CH1232466A patent/CH490421A/de not_active IP Right Cessation
- 1966-08-31 IL IL26433A patent/IL26433A/en unknown
- 1966-08-31 NL NL6612312A patent/NL6612312A/xx unknown
- 1966-08-31 ES ES0330802A patent/ES330802A1/es not_active Expired
- 1966-09-01 BE BE686314D patent/BE686314A/xx unknown
- 1966-09-01 AT AT01444/67A patent/AT284542B/de not_active IP Right Cessation
- 1966-09-02 GB GB39418/66A patent/GB1160693A/en not_active Expired
- 1966-09-02 BR BR182588/66A patent/BR6682588D0/pt unknown
- 1966-09-06 US US577197A patent/US3502690A/en not_active Expired - Lifetime
-
1967
- 1967-05-13 ES ES340546A patent/ES340546A1/es not_active Expired
Non-Patent Citations (1)
| Title |
|---|
| None * |
Also Published As
| Publication number | Publication date |
|---|---|
| IL26433A (en) | 1970-12-24 |
| BR6682588D0 (pt) | 1973-12-04 |
| BE686314A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1967-03-01 |
| ES330802A1 (es) | 1967-09-16 |
| AT284542B (de) | 1970-09-25 |
| ES340546A1 (es) | 1968-10-01 |
| GB1160693A (en) | 1969-08-06 |
| NL6612312A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1967-03-06 |
| NL131206C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| US3502690A (en) | 1970-03-24 |
| CH490421A (de) | 1970-05-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69028461T2 (de) | Triazin-derivate und unkrautvertilgungsmittel daraus | |
| DE1238902B (de) | Verfahren zur Herstellung von Phosphor-, Phosphon- bzw. Thionophosphor-, -phosphon-saeureestern | |
| DE1298531B (de) | Verfahren zur Herstellung von Organozinnkomplexen | |
| EP0106243A1 (de) | Azolyl-methylamine, ihre Herstellung und Verwendung in mikrobiziden Mitteln | |
| DE1239695B (de) | Verfahren zur Herstellung von Phosphor-, Phosphon-, Thionophosphor- oder Thiono-phosphonsaeureestern | |
| DE1172667B (de) | Verfahren zur Herstellung von O, O-Dialkyl-S-alkylthiolphosphorsaeureestern | |
| AT258307B (de) | Verfahren zur Herstellung von neuen Zinnkomplexverbindungen | |
| DE2126149A1 (en) | Halo-salicylanilide derivs - with acaricidal and fungicidal activity | |
| DE1223381B (de) | Verfahren zur Herstellung von Amidido-(thio)-phosphor-(-phosphon-)-saeureestern | |
| DE1670896C3 (de) | Pyridylphosphor-, -phosphon- bzw. -thionophosphor- (-phosphon-) -säureester, Verfahren zu deren Herstellung sowie diese enthaltende Mittel | |
| DE1183494B (de) | Verfahren zur Herstellung von Phosphor-, Phosphon- bzw. Thionophosphor-, -phosphonsaeureestern | |
| DE1215709B (de) | Verfahren zur Herstellung von Sulfoxid-Zinnkomplexverbindungen | |
| CH509750A (de) | Fungitoxisches Mittel | |
| DE2260719A1 (de) | Verfahren zur herstellung von amidomethylphosphonsaeureestern | |
| DE1150972B (de) | Verfahren zur Herstellung von Thio- bzw. Dithiophosphor-(-on, -in)-saeureestern | |
| DE1193036B (de) | Verfahren zur Herstellung von Phosphor-, Phosphon-, Phosphin- bzw. Thiophosphor-, -phosphon-, -phosphinsaeureestern | |
| DE1192202B (de) | Verfahren zur Herstellung von (Thiono) Phosphor-(on, in)-saeureestern | |
| AT250987B (de) | Verfahren zur Herstellung von neuen Zinnkomplexsalzen | |
| DE1668103C3 (de) | Verfahren zur Herstellung von Chloralkyl-S-alkyl-bzw. -aryl-(di)thiolphosphorsäurediesteramiden bzw. -ersterdiamiden | |
| CH524312A (de) | Verwendung von Organozinnazoliden zur Bekämpfung von Fungi und Mikroben | |
| CH420122A (de) | Verfahren zur Herstellung von Thiophosphor-(-phosphon-, -phosphin)- bzw. Dithiophosphor-(-phosphon-, -phosphin)-säureestern | |
| DE2022494A1 (de) | Fungizide Mittel | |
| DE2019844A1 (de) | Fungitoxische Formylaminale | |
| DE2056652A1 (de) | Fungizide und mikrobizide Mittel | |
| DE1814252A1 (de) | N-Acyl-dicyanocarbonyl-phenylhydrazone |