AR034030A1 - Fluoralcoxifenilsulfonilamino (tio) carbonil-triazolin-(tio)onas substituidas, procedimiento para su obtencion, metodo para la lucha contra el crecimiento indeseable de las plantas, uso de estos compuestos para la lucha contra las plantas indeseables, y composicion herbicida - Google Patents
Fluoralcoxifenilsulfonilamino (tio) carbonil-triazolin-(tio)onas substituidas, procedimiento para su obtencion, metodo para la lucha contra el crecimiento indeseable de las plantas, uso de estos compuestos para la lucha contra las plantas indeseables, y composicion herbicidaInfo
- Publication number
- AR034030A1 AR034030A1 ARP020101108A ARP020101108A AR034030A1 AR 034030 A1 AR034030 A1 AR 034030A1 AR P020101108 A ARP020101108 A AR P020101108A AR P020101108 A ARP020101108 A AR P020101108A AR 034030 A1 AR034030 A1 AR 034030A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- fluorine
- ethoxy
- propoxy
- methoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- -1 methoxy, ethoxy Chemical group 0.000 abstract 21
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 7
- 239000000460 chlorine Substances 0.000 abstract 7
- 229910052801 chlorine Inorganic materials 0.000 abstract 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 5
- 229910052794 bromium Inorganic materials 0.000 abstract 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 229910052731 fluorine Inorganic materials 0.000 abstract 4
- 239000011737 fluorine Substances 0.000 abstract 4
- CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 abstract 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 2
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 abstract 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 2
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 2
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 abstract 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 2
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 abstract 1
- 125000006309 butyl amino group Chemical group 0.000 abstract 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 abstract 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 abstract 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 230000008635 plant growth Effects 0.000 abstract 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 abstract 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Indole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Fluoralcoxifenilsulfonilamino (tio) carbonil-triazolin-(tio) onas sustituidas que tiene la fórmula general (1), en la que n significa los números 2, 3 o 4; Q1 significa O (oxígeno) o S (azufre); Q2 significa O (oxígeno) o S (azufre); R1 significa metilo, etilo, n- o i-propilo, n-, i-, s- o t-butilo, metoxi, etoxi, n- o i-propoxi, n-, i-, s- o t-butoxi, metoxicarbonilo, etoxicarbonilo, n- o i-propoxicarbonilo sustituidos respectiva, opcionalmente con ciano, con flúor, con cloro, con bromo, con metoxi, con etoxi, con n- o i-propoxi; R2 significa hidrógeno, ciano, flúor, cloro, bromo, significa metilo, etilo, n- o i-propilo, n-, i-, s- o t-butilo, metoxi, etoxi, n- o i-propoxi, n-, i-, s- o t-butoxi, metiltio, etiltio, n- o i-propiltio, n-, i-, s- o t- butiltio, metilamino, etilamino, n- o i- propilamino, n-, i-, s- o t- butilamino, metoxiamino, etoxiamino, n- o i- propoxiamino, n-, i-, s- o t- butoxiamino sustituidos respectiva y opcionalmente con ciano, con flúor, con cloro, con metoxi, con etoxi, con n- o i-propoxi, significa dimetilamino, dietilamino, N-metil-metoxiamino o N-metil-etoxiamino, significa etenilo, propenilo, butenilo, etinilo, propinilo, butinilo, propeniloxi, buteniloxi, propiniloxi, butiniloxi, propeniltio, buteniltio, propiniltio, butiniltio, propenilamino, butenilamino, propinilamino o butinilamino sustituidos respectiva y opcionalmente con ciano, con flúor, con cloro o con bromo, o significa ciclopropilo, ciclobutilo, ciclopentilo, ciclohexilo, ciclopropiloxi, ciclobutiloxi, ciclopentiloxi, ciclohexiloxi, ciclopropilamino, ciclobutilamino, ciclopentilamino, ciclohexilamino, ciclopropilmetilo, ciclobutilmetilo, ciclopentilmetilo, ciclohexilmetilo, ciclopropilmetoxi, ciclobutilmetoxi, ciclopentilmetoxi, ciclohexilmetoxi, ciclopropilmetiltio, ciclobutilmetiltio, ciclopentilmetiltio, ciclohexilmetiltio, ciclopropilmeilamino, ciclobutilmetilamino, ciclopentilmetilamino o ciclohexilmetilamino sustituidos respectiva y opcionalmente con ciano, con flúor, con cloro, con bromo, con metilo o con etilo, y R2 significa hidrógeno, significa metilo, etilo, n- o i-propilo, metoxi, etoxi, n- o i-propoxi, metilamino, etilamino, n- o i-propilamino sustituidos respectiva y opcionalmente con ciano, con flúor, con cloro, con metoxi, con etoxi, por n- o i-propoxi, significa dimetilamino o dietilamino, o significa ciclopropilo, ciclobutilo, ciclopentilo, ciclohexilo, ciclopropilmetilo, ciclobutilmetilo, ciclopentilmetilo o ciclohexilmetilo sustituidos respectiva y opcionalmente con ciano, con flúor, con cloro, con bromo, con metilo, o con etilo, así como las sales de los compuestos de la fórmula (1), quedando excluidos por renuncia a su reivindicación los compuestos 2-(2-flúor-etoxi)-6-metil-N-[(4-metil-5-oxo-3-propoxi-4,5-dihidro-1H-1,2,4-triazol-1-il)-carbonil]-bencenosulfonamida, 2-(2-flúor-etoxi)-6-metil-N-[(4-metil-5-oxo-3-i-propoxi-4,5-dihidro-1H-1,2,4-triazol-1-il)-carbonil]-bencenosulfonamida, 2-(2-flúor-etoxi)-6-metil-N-[4-ciclopropil3-metoxi-5-oxo-4,5-dihidro-1H-1,2,4-triazol-1-il)-carbonil]-bencenosulfonamida, 2-(2-flúor-etoxi)-6-metil-N-[4-ciclopropil-5-oxo-3-i-propoxi-4,5-dihidro-1H-1,2,4-triazol-1-il)-carbonil]bencenosulfonamida, 2-(2-flúor-etoxi)-6-metil-N-[3-metoxi-4-metil-5-oxo-4,5-dihidro-1H-1,2,4-triazol-1-il)-carbonil]-bencenosulfonamida, 2-(2-flúor-etoxi)-6-metil-N-[3-etoxi-4-metil-5-oxo-4,5-dihidro-1H-1,2,4-triazol-1-il)-carbonil]-bencenosulfonamida y 2-(2-flúor-etoxi)-6-metil-N-[3,4-dimetil-5-oxo-4,5-dihidro-1H-1,2,4-triazol-1-il)-carbonil]-bencenosulfonamida, procedimiento para su obtención, método para la lucha contra el crecimiento indeseable de las plantas, uso de estos compuestos para la lucha contra las plantas indeseables, y composición herbicida.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10117673A DE10117673A1 (de) | 2001-04-09 | 2001-04-09 | Substituierte Fluoralkoxyphenylsulfonylamino(thio)carbonyl-triazolin(thi)one |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR034030A1 true AR034030A1 (es) | 2004-01-21 |
Family
ID=7680957
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020101108A AR034030A1 (es) | 2001-04-09 | 2002-03-26 | Fluoralcoxifenilsulfonilamino (tio) carbonil-triazolin-(tio)onas substituidas, procedimiento para su obtencion, metodo para la lucha contra el crecimiento indeseable de las plantas, uso de estos compuestos para la lucha contra las plantas indeseables, y composicion herbicida |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20040157744A1 (es) |
| EP (1) | EP1379512A1 (es) |
| JP (1) | JP2004526754A (es) |
| KR (1) | KR20040011484A (es) |
| CN (1) | CN100354269C (es) |
| AR (1) | AR034030A1 (es) |
| AU (1) | AU2002257720B2 (es) |
| BR (1) | BR0208755A (es) |
| CA (1) | CA2443385A1 (es) |
| DE (1) | DE10117673A1 (es) |
| MX (1) | MXPA03009157A (es) |
| PL (1) | PL363035A1 (es) |
| RU (1) | RU2309151C2 (es) |
| UA (1) | UA78204C2 (es) |
| WO (1) | WO2002081458A1 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1717228A1 (de) | 2005-04-28 | 2006-11-02 | Bayer CropScience GmbH | Sulfonylamino(thio)carbonylverbindungen als Herbizide oder Pflanzenwachstumsregulatoren |
| DE202008005350U1 (de) | 2008-04-17 | 2008-07-03 | BSH Bosch und Siemens Hausgeräte GmbH | Abstellbehälter für ein Kältegerät |
| CN103130731B (zh) * | 2013-03-06 | 2015-06-03 | 陕西科技大学 | 一种制备4-氨基-5-芳基-1,2,4-三唑-3-硫酮的方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1330438C (en) * | 1980-07-17 | 1994-06-28 | Willy Meyer | N-phenylsulfonyl-n'-pyrimidinyl-and-triazinylureas |
| DE3431916A1 (de) * | 1984-08-30 | 1986-03-13 | Bayer Ag, 5090 Leverkusen | Fluoralkoxyphenylsulfonylguanidine |
| US5276162A (en) * | 1988-05-09 | 1994-01-04 | Bayer Aktiengesellschaft | Herbicidal sulphonylaminocarbonyltriazolinones having substituents which are bonded via sulphur |
| DE3815765A1 (de) * | 1988-05-09 | 1989-11-23 | Bayer Ag | 2-sulfonylaminocarbonyl-2,4-dihydro-3h-1,2,4- triazol-3-one einschliesslich 4,5-kondensierter, bicyclischer derivate, verfahren und neue zwischenprodukte zu ihrer herstellung und ihre verwendung als pflanzenbehandlungsmittel |
| US5149356A (en) * | 1988-05-09 | 1992-09-22 | Bayer Aktiengesellschaft | Herbicidal sulphonylaminocarbonyltriazolinones having substituents which are bonded via sulphur |
| US5085684A (en) * | 1988-05-09 | 1992-02-04 | Bayer Aktiengesellschaft | Herbicidal sulphonylaminocarbonyltriazolinones having substituents which are bonded via sulphur |
| US5057144A (en) * | 1988-05-09 | 1991-10-15 | Bayer Aktiengesellschaft | Sulphonylaminocarbonyltriazolinones |
| US5241074A (en) * | 1988-05-09 | 1993-08-31 | Bayer Aktiengesellschaft | Sulphonylaminocarbonyltriazolinones |
| US5094683A (en) * | 1988-05-09 | 1992-03-10 | Bayer Aktiengesellschaft | Sulphonylaminocarbonyltriazolinones |
| US5238910A (en) * | 1989-11-03 | 1993-08-24 | Bayer Aktiengesellschaft | Herbicidal halogenated sulphonylaminocarbonyltriazolinones |
| DE4017338A1 (de) * | 1990-05-30 | 1991-12-05 | Bayer Ag | Sulfonylierte carbonsaeureamide |
| US5534486A (en) * | 1991-04-04 | 1996-07-09 | Bayer Aktiengesellschaft | Herbicidal sulphonylaminocarbonyl triazolinones having substituents bonded via oxygen |
| DE4234801A1 (de) * | 1992-10-15 | 1994-04-21 | Bayer Ag | Sulfonylaminocarbonyltriazolinone |
| US6077813A (en) * | 1994-05-04 | 2000-06-20 | Bayer Aktiengesellschaft | Substituted aromatic thiocarboxylic acid amides and their use as herbicides |
| DE19508119A1 (de) * | 1995-03-08 | 1996-09-12 | Bayer Ag | Sulfonylaminocarbonyltriazolinone mit Halogenalkylthio-Substituenten |
| DE19525162A1 (de) * | 1995-07-11 | 1997-01-16 | Bayer Ag | Sulfonylamino(thio)carbonylverbindungen |
-
2001
- 2001-04-09 DE DE10117673A patent/DE10117673A1/de not_active Withdrawn
-
2002
- 2002-03-26 AR ARP020101108A patent/AR034030A1/es unknown
- 2002-03-27 PL PL02363035A patent/PL363035A1/xx not_active Application Discontinuation
- 2002-03-27 WO PCT/EP2002/003404 patent/WO2002081458A1/de not_active Ceased
- 2002-03-27 BR BR0208755-3A patent/BR0208755A/pt not_active IP Right Cessation
- 2002-03-27 RU RU2003132535/04A patent/RU2309151C2/ru active
- 2002-03-27 US US10/474,184 patent/US20040157744A1/en not_active Abandoned
- 2002-03-27 KR KR10-2003-7012388A patent/KR20040011484A/ko not_active Ceased
- 2002-03-27 CA CA002443385A patent/CA2443385A1/en not_active Abandoned
- 2002-03-27 MX MXPA03009157A patent/MXPA03009157A/es not_active Application Discontinuation
- 2002-03-27 CN CNB028079841A patent/CN100354269C/zh not_active Expired - Fee Related
- 2002-03-27 UA UA20031110064A patent/UA78204C2/uk unknown
- 2002-03-27 EP EP02727485A patent/EP1379512A1/de not_active Withdrawn
- 2002-03-27 AU AU2002257720A patent/AU2002257720B2/en not_active Ceased
- 2002-03-27 JP JP2002579446A patent/JP2004526754A/ja not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| UA78204C2 (en) | 2007-03-15 |
| KR20040011484A (ko) | 2004-02-05 |
| JP2004526754A (ja) | 2004-09-02 |
| PL363035A1 (en) | 2004-11-15 |
| US20040157744A1 (en) | 2004-08-12 |
| CN1501920A (zh) | 2004-06-02 |
| RU2003132535A (ru) | 2005-04-20 |
| DE10117673A1 (de) | 2002-10-10 |
| CN100354269C (zh) | 2007-12-12 |
| RU2309151C2 (ru) | 2007-10-27 |
| EP1379512A1 (de) | 2004-01-14 |
| WO2002081458A1 (de) | 2002-10-17 |
| BR0208755A (pt) | 2004-05-11 |
| MXPA03009157A (es) | 2004-02-12 |
| CA2443385A1 (en) | 2002-10-17 |
| AU2002257720B2 (en) | 2008-05-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |