AR013891A1 - PESTICIDE ACTIVE COMPOUNDS, A PROCESS FOR PREPARATION, A PESTICIATED COMPOSITION, A PROCESS FOR THE PREPARATION OF A COMPOSITIONED COMPOSITION, INTERMEDIARIES FOR PREPARATION, A METHOD FOR CONTROLLING PESTS AND THE PLANT PROPAGATION MATERIAL. - Google Patents
PESTICIDE ACTIVE COMPOUNDS, A PROCESS FOR PREPARATION, A PESTICIATED COMPOSITION, A PROCESS FOR THE PREPARATION OF A COMPOSITIONED COMPOSITION, INTERMEDIARIES FOR PREPARATION, A METHOD FOR CONTROLLING PESTS AND THE PLANT PROPAGATION MATERIAL.Info
- Publication number
- AR013891A1 AR013891A1 ARP970106002A AR013891A1 AR 013891 A1 AR013891 A1 AR 013891A1 AR P970106002 A ARP970106002 A AR P970106002A AR 013891 A1 AR013891 A1 AR 013891A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- preparation
- haloalkyl
- alkoxy
- composition
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C251/36—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atoms of the oxyimino groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C251/40—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atoms of the oxyimino groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C251/36—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atoms of the oxyimino groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C251/38—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atoms of the oxyimino groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/50—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals
- C07C251/60—Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals of hydrocarbon radicals substituted by carboxyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Un compuesto de la formula (I), en donde, cualquiera de: X es CH o N, Y es OR1 y Z es O, o X es N; Y es NHR8; y Z es O, S, o S(=O); U es formula (II); R1es H o alquilo C1-4; R2 es H, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, cicloalquenilo C3-6, alcoxi C1-4 metilo, alcoxi C1-4, haloalcoxi C1-4,tioalquilo C1-4, o halotioalquilo C1-4, ciano, o arilo; R3 y R4 son cada uno independientemente del otro, H, alquilo C1-4, alcoxi C1-4, OH, SH, NH2, CN,NO2, un grupo (alquilo C1-4)3-Si, siendo posible que los grupos alquilo sean iguales o diferentes, halogeno, (alquilo C1-4)S(=O)1, (haloalquilo C1-4)S(=O)1, haloalquilo C1-4, o haloalcoxi C1-4, alquilo C1-6 amino, dialquilo C1-6 amino, siendo posible que los grupos alquilo sean iguales o diferentes;arilamino o diarilamino, siendo posible que los grupos arilo sean iguales o diferentes; l es 0, 1 o 2; R5 y R6 son cada uno independientemente del otro,alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, cicloalquenilo C3-6, halocicloalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, tioalquilo C1-6,halotioalquilo C1-6, alquilo C1-6 sulfinilo, haloalquilo C1-6 sulfinilo, alquilo C1-6 sulfonilo, haloalquilo C1-6 sulfonilo, alquilo C1-6 sulfoniloxi,haloalquilo C1-6 sulfoniloxi, alcoxi C1-6 alquilo C1-6, haloalcoxi C1-6 alquilo C1-6, alcoxi C1-6 alcoxi C1-6, tioalquilo C1-6 alquilo C1-6, haloalquiloC1-6 tioalquilo C1-6, alquilo C1-6 sulfinilalquilo C1-6, haloalquilo C1-6 sulfinilalquilo C1-6, alquilo C1-6 sulfonilalquilo C1-6, haloalquilo C1-6sulfonilalquilo C1-6, formilo, -CH=NO-alquilo C1-8, -CH=NO-alquenilo C2-8, -CH=NO-alquinilo C2-8, -CH=NO-cicloalquilo C3-6, alquilo C1-6 carbonilo,haloalquilo C1-6 carbonilo, alcoxi C1-6 carbonilo, haloalcoxi C1-6 carbonilo, alquilo C1-6 aminocarbonilo, alcoxi C1-4 iminometilo, di(alquilo C1-6)A compound of the formula (I), wherein, any of: X is CH or N, Y is OR1 and Z is O, or X is N; Y is NHR8; and Z is O, S, or S (= O); U is formula (II); R1 is H or C1-4 alkyl; R 2 is H, C 1-4 alkyl, C 1-4 haloalkyl, C 3-6 cycloalkyl, C 3-6 cycloalkenyl, C 1-4 alkoxy, C 1-4 alkoxy, C 1-4 haloalkoxy, C 1-4 thioalkyl, or C 1-4 halothioalkyl , cyano, or aryl; R3 and R4 are each independently of each other, H, C1-4 alkyl, C1-4 alkoxy, OH, SH, NH2, CN, NO2, a group (C1-4 alkyl) 3-Si, it being possible that the alkyl groups are the same or different, halogen, (C1-4 alkyl) S (= O) 1, (C1-4 haloalkyl) S (= O) 1, C1-4 haloalkyl, or C1-4 haloalkoxy, C1-6 amino alkyl, C1-6 amino dialkyl, it being possible that the alkyl groups are the same or different, arylamino or diarylamino, it being possible that the aryl groups are the same or different; l is 0, 1 or 2; R 5 and R 6 are each independently of the other, C 1-6 alkyl, C 1-6 haloalkyl, C 3-6 cycloalkyl, C 3-6 cycloalkenyl, C 3-6 halocycloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, C 1-6 thioalkyl, C1-6 halothioalkyl, C1-6 alkyl sulfinyl, haloalkyl C1-6 sulfinyl, C1-6 alkyl sulfonyl, haloalkyl C1-6 sulfonyl, C1-6 alkyl sulfonyloxy, haloalkyl C1-6 sulfonyloxy, C1-6 alkoxy C1-6 alkyl, C1-6 haloalkoxy C1-6 alkyl, C1-6 alkoxy C1-6 alkoxy, C1-6 thioalkyl C1-6 alkyl, halo C1-6 alkylthio C1-6 alkyl, C1-6 alkyl sulfinylalkyl C1-6, haloalkyl C1-6 sulfinylalkyl C1 -6, C1-6 alkyl sulfonylalkyl C1-6, haloalkyl C1-6 sulfonylalkyl C1-6, formyl, -CH = NO-C1-8 alkyl, -CH = NO-C2-8 alkenyl, -CH = NO-C2- alkynyl 8, -CH = NO3-6 cycloalkyl, C1-6 carbonyl alkyl, C1-6 haloalkyl carbonyl, C1-6 carbonyl alkoxy, C1-6 haloalkoxycarbonyl, C1-6 aminocarbonyl alkyl, C1-4 iminomethyl alkoxy, di ( C1-6 alkyl)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH313996 | 1996-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR013891A1 true AR013891A1 (en) | 2001-01-31 |
Family
ID=4249454
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP970106002 AR013891A1 (en) | 1996-12-20 | 1997-12-18 | PESTICIDE ACTIVE COMPOUNDS, A PROCESS FOR PREPARATION, A PESTICIATED COMPOSITION, A PROCESS FOR THE PREPARATION OF A COMPOSITIONED COMPOSITION, INTERMEDIARIES FOR PREPARATION, A METHOD FOR CONTROLLING PESTS AND THE PLANT PROPAGATION MATERIAL. |
Country Status (4)
Country | Link |
---|---|
AR (1) | AR013891A1 (en) |
AU (1) | AU5760098A (en) |
WO (1) | WO1998028262A1 (en) |
ZA (1) | ZA9711419B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000017155A1 (en) * | 1998-09-22 | 2000-03-30 | Bayer Aktiengesellschaft | Pesticidal bis-oxime compounds |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995018789A1 (en) * | 1994-01-05 | 1995-07-13 | Ciba-Geigy Ag | Pesticides |
SK282298B6 (en) * | 1994-02-04 | 2002-01-07 | Basf Aktiengesellschaft | Phenylacetic acid derivatives, method and intermediates of their production, their use and substances containing them |
CA2203507A1 (en) * | 1994-11-17 | 1996-05-30 | Rene Zurfluh | O-benzyl oxime ether derivatives and their use as pesticides |
WO1997001530A1 (en) * | 1995-06-27 | 1997-01-16 | Novartis Ag | O-benzyl oxime ether derivatives and their use in crop protection compositions |
-
1997
- 1997-12-18 AU AU57600/98A patent/AU5760098A/en not_active Abandoned
- 1997-12-18 AR ARP970106002 patent/AR013891A1/en unknown
- 1997-12-18 WO PCT/EP1997/007122 patent/WO1998028262A1/en active Application Filing
- 1997-12-19 ZA ZA9711419A patent/ZA9711419B/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO1998028262A1 (en) | 1998-07-02 |
AU5760098A (en) | 1998-07-17 |
ZA9711419B (en) | 1998-06-22 |
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