DE2532767A1 - Triazin-derivate als schaedlingsbekaempfungsmittel - Google Patents
Triazin-derivate als schaedlingsbekaempfungsmittelInfo
- Publication number
- DE2532767A1 DE2532767A1 DE19752532767 DE2532767A DE2532767A1 DE 2532767 A1 DE2532767 A1 DE 2532767A1 DE 19752532767 DE19752532767 DE 19752532767 DE 2532767 A DE2532767 A DE 2532767A DE 2532767 A1 DE2532767 A1 DE 2532767A1
- Authority
- DE
- Germany
- Prior art keywords
- och
- formula
- compound
- methoxy
- sch
- 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- Withdrawn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
- 150000003918 triazines Chemical class 0.000 title description 4
- 239000004480 active ingredient Substances 0.000 claims description 34
- 150000001875 compounds Chemical class 0.000 claims description 34
- 241000196324 Embryophyta Species 0.000 claims description 25
- -1 C 9 -C Chemical group 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 239000004009 herbicide Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 239000002585 base Substances 0.000 claims description 4
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 4
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 4
- 230000002363 herbicidal effect Effects 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims description 3
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- 238000002360 preparation method Methods 0.000 claims description 3
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 2
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- 239000003513 alkali Substances 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
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- 239000011593 sulfur Substances 0.000 claims description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
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- 239000002202 Polyethylene glycol Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
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- 244000062793 Sorghum vulgare Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical group C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- QLVWRJVCAROATI-UHFFFAOYSA-N 2-azido-1,3,5-triazine Chemical compound [N-]=[N+]=NC1=NC=NC=N1 QLVWRJVCAROATI-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
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- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
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- 102100026197 C-type lectin domain family 2 member D Human genes 0.000 description 1
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- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000006000 trichloroethyl group Chemical group 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/48—Two nitrogen atoms
- C07D251/52—Two nitrogen atoms with an oxygen or sulfur atom attached to the third ring carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1026874A CH588213A5 (en, 2012) | 1974-07-25 | 1974-07-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2532767A1 true DE2532767A1 (de) | 1976-02-12 |
Family
ID=4361347
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19752532767 Withdrawn DE2532767A1 (de) | 1974-07-25 | 1975-07-22 | Triazin-derivate als schaedlingsbekaempfungsmittel |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4007032A (en, 2012) |
| JP (1) | JPS5138426A (en, 2012) |
| AT (1) | AT345610B (en, 2012) |
| BE (1) | BE831684A (en, 2012) |
| CA (1) | CA1050545A (en, 2012) |
| CH (1) | CH588213A5 (en, 2012) |
| DE (1) | DE2532767A1 (en, 2012) |
| ES (1) | ES439696A1 (en, 2012) |
| FR (1) | FR2279736A1 (en, 2012) |
| GB (1) | GB1477955A (en, 2012) |
| IL (1) | IL47812A (en, 2012) |
| IT (1) | IT1044012B (en, 2012) |
| NL (1) | NL7508800A (en, 2012) |
| SU (1) | SU667099A3 (en, 2012) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0226536A3 (de) * | 1985-12-02 | 1988-06-15 | Ciba-Geigy Ag | (Di)alkoxycarbonyl-amino-s-triazin-Derivate gegen tier- und pflanzenparasitäre Schädlinge |
| WO2000032580A3 (en) * | 1998-12-01 | 2000-08-17 | Bayer Agrochem Kk | Substituted 1,3,5-triazines as herbicides |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4160832A (en) * | 1976-08-19 | 1979-07-10 | Ciba-Geigy Corporation | Novel insecticides |
| DE3222147A1 (de) * | 1982-06-11 | 1983-12-15 | Chemische Werke Hüls AG, 4370 Marl | Verwendung gegebenenfalls substituierter thiomethylcycloalkylamino-s-triazine als selektive mittel gegen unkraeuter und schadgraeser |
| DE3322720A1 (de) * | 1983-06-24 | 1985-01-03 | Chemische Werke Hüls AG, 4370 Marl | Verwendung von in 2-stellung mit (substituierten) aminogruppen substituierten 4-dl-alkylester-(alpha)-alaninyl-6-chlor-s-triazinen als herbizide, insbesondere gegen flughafer |
| US4528027A (en) * | 1984-05-24 | 1985-07-09 | Shell Oil Company | Acylthio-substituted triazines |
| DE19924370A1 (de) * | 1999-05-27 | 2000-11-30 | Bayer Ag | Substituierte Cyclohexylalkylamino-1,3,5-triazine |
| DE102007025451B4 (de) * | 2007-05-31 | 2013-03-28 | Ami Agrolinz Melamine International Gmbh | Triazinderivate |
| WO2008156151A1 (ja) * | 2007-06-19 | 2008-12-24 | Kobelco Eco-Solutions Co., Ltd. | シミュレーション方法、シミュレーション装置、生物処理方法、ならびに、生物処理装置 |
| DE102008061139A1 (de) * | 2008-12-09 | 2010-06-10 | Borealis Agrolinz Melamine Gmbh | Verfahren zur Herstellung von Triazincarbamaten unter Verwendung von Chlorformiaten |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE617033A (en, 2012) | 1961-04-28 | |||
| CH550546A (de) * | 1971-08-05 | 1974-06-28 | Ciba Geigy Ag | Herbizides mittel. |
-
1974
- 1974-07-25 CH CH1026874A patent/CH588213A5/xx not_active IP Right Cessation
-
1975
- 1975-07-21 US US05/597,608 patent/US4007032A/en not_active Expired - Lifetime
- 1975-07-22 FR FR7522789A patent/FR2279736A1/fr active Granted
- 1975-07-22 DE DE19752532767 patent/DE2532767A1/de not_active Withdrawn
- 1975-07-23 NL NL7508800A patent/NL7508800A/xx not_active Application Discontinuation
- 1975-07-23 CA CA232,107A patent/CA1050545A/en not_active Expired
- 1975-07-24 GB GB3102875A patent/GB1477955A/en not_active Expired
- 1975-07-24 IT IT25712/75A patent/IT1044012B/it active
- 1975-07-24 SU SU752157427A patent/SU667099A3/ru active
- 1975-07-24 AT AT572775A patent/AT345610B/de not_active IP Right Cessation
- 1975-07-24 ES ES439696A patent/ES439696A1/es not_active Expired
- 1975-07-24 JP JP50090693A patent/JPS5138426A/ja active Pending
- 1975-07-24 BE BE158568A patent/BE831684A/xx unknown
- 1975-07-25 IL IL47812A patent/IL47812A/xx unknown
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0226536A3 (de) * | 1985-12-02 | 1988-06-15 | Ciba-Geigy Ag | (Di)alkoxycarbonyl-amino-s-triazin-Derivate gegen tier- und pflanzenparasitäre Schädlinge |
| WO2000032580A3 (en) * | 1998-12-01 | 2000-08-17 | Bayer Agrochem Kk | Substituted 1,3,5-triazines as herbicides |
| US6645915B1 (en) | 1998-12-01 | 2003-11-11 | Nihon Bayer Agrochem K. K. | Substituted 1,3,5- triazines |
| RU2252937C2 (ru) * | 1998-12-01 | 2005-05-27 | Нихон Байер Агрохем К.К. | Производные 1,3,5-триазина, гербицидная композиция на их основе и промежуточные соединения |
Also Published As
| Publication number | Publication date |
|---|---|
| IL47812A (en) | 1979-01-31 |
| CA1050545A (en) | 1979-03-13 |
| IT1044012B (it) | 1980-02-29 |
| JPS5138426A (en, 2012) | 1976-03-31 |
| GB1477955A (en) | 1977-06-29 |
| ES439696A1 (es) | 1977-03-16 |
| BE831684A (fr) | 1976-01-26 |
| AT345610B (de) | 1978-09-25 |
| CH588213A5 (en, 2012) | 1977-05-31 |
| FR2279736A1 (fr) | 1976-02-20 |
| IL47812A0 (en) | 1975-10-15 |
| ATA572775A (de) | 1978-01-15 |
| FR2279736B1 (en, 2012) | 1977-12-09 |
| NL7508800A (nl) | 1976-01-27 |
| SU667099A3 (ru) | 1979-06-05 |
| US4007032A (en) | 1977-02-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8141 | Disposal/no request for examination |