Title:
【発明の名称】パーハロアルコキシベンゼノフェノンヒドラゾンおよび有害生物防除剤としてのそれらの用途
Document Type and Number:
Japanese Patent JPH10504799
Kind Code:
A
Abstract:
Compounds of formula (I) in which X is (a) or (b), n is 0, 1, 2, 3, 4 or 5, where if n is greater than 1, the radicals R2 are identical or different; o is 0, 1, 2, 3 or 4, where if o is greater than 1, the radicals R3 are identical or different; R1 is perhalo-C1-C4alkoxy; R2 is halogen, C1-C8alkyl, halo-C1-C8alkyl, C1-C8alkoxy, halo-C1-C8alkoxy, C1-C8alkylthio, halo-C1-C8alkylthio, C1-C8alkylsulfynyl, halo-C1-C8alkylsulfynyl, C1-C8alkylsulfonyl, halo-C1-C8alkylsulfonyl, CN or phenyl; R3 is halogen, C1-C8alkyl, halo-C1-C8alkyl or halo-C1-C8alkoxy; R4 is H, halogen, C1-C8alkyl, C3-C6cycloalkyl, halo-C1-C8alkyl, C1-C8alkoxy, C1-C8alkoxy-C1-C8alkyl, C1-C8alkoxy-C1-C8alkoxy, C1-C8alkylthio or NR8R9; R5 is C1-C8alkyl, NR10R11, OR20, SR20 or SO2R20; R6 is H, C1-C8alkyl, C3-C6cycloalkyl, halo-C1-C8alkyl, C1-C8alkenyl, C1-C8alkynyl, C1-C8acyl or phenyl; R7 is H, an unsubstituted or substituted C1-C8alkyl, C3-C6cycloakyl, C3-C6cycloalkyl-C1-C8alkyl, C1-C8alkenyl, C1-C8alkynyl, C3-C6cycloalkenyl, C3-C6cycloalkenyl-C1-C8alkyl or C3-C6cycloalkyl-C1-C8alkenyl group, it being possible for the substituents to be selected from the group consisting of halogen, C1-C8alkyl, halo-C1-C8alkyl, C1-C8alkoxy, halo-C1-C8alkoxy, C1-C8alkyl-S(O)p, it being possible for p to be 0, 1 or 2, C1-C8alkoxycarbonyl, di(C1-C8alkyl)amino and C1-C8alkanoyloxy; an unsubstituted or substituted phenyl or heteroaryl group, it being possible for the substituents to be selected from the group consisting of C1-C6alkyl and halogen; C1-C8alkoxy, NR16R17, COOR6 or SR6; R8 and R9 independently of one another are H, C1-C8alkyl or OH; R10 is H, C1-C8alkyl, C3-C6cycloalkyl, halo-C1-C8alkyl, halo-C1-C8alkoxy-C1-C8alkyl, phenyl, OR12, S(O)mR13, m being 0, 1 or 2, or NR14R15; R11 is H, C1-C8alkyl, C3-C6cycloalkyl, halo-C1-C8alkyl, C1-C8alkoxy-C1-C8alkyl, allyl, C1-C8alkylallyl, haloallyl or propargyl; R12 is H, C1-C8alkyl, halo-C1-C8alkyl, C1-C8alkoxy-C1-C8alkyl, C3-C6cycloalkyl, C2-C8alkenyl, halo-C2-C8alkenyl or propargyl; R13 is H, C1-C8alkyl, halogen-C1-C8alkyl, phenyl or NR14R15; R14 and R15 independently of one another are H, C1-C8alkyl, halo-C1-C8alkyl, phenyl, C1-C8alkylamido, di(C1-C8alkyl)amido or NH2; R16 and R17 independently of one another are H, C1-C8alkyl, halo-C1-C8alkyl, C2-C8alkenyl, C1-C8alkoxy or NH2; R18 is S(O)mR19, m being 0, 1 or 2, NO2 or CN; R19 is C1-C8alkyl, halo-C1-C8alkyl, C3-C6cycloalkyl, phenyl, benzyl or NR14R15; R20 is C1-C8alkyl, halo-C1-C8alkyl or C3-C6cycloalkyl; Y is O, S, NR18 or CHC(O)R21; and R21 is H, C1-C8alkyl, halo-C1-C8alkyl, C1-C8alkoxy or phenyl, and if appropriate, E/Z isomers and tautomers thereof, in each case in free form or in salt form, can be used as agrochemical active ingredients and may be prepared in a manner known per se.
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Inventors:
Pasqual, Alphonse
Hall, Roger Graham
Dur, Dieter
Hall, Roger Graham
Dur, Dieter
Application Number:
JP52795795A
Publication Date:
May 12, 1998
Filing Date:
April 15, 1995
Export Citation:
Assignee:
Novartis Actien Gezel Shaft
International Classes:
A01N35/10; A01N37/28; A01N37/44; A01N37/52; A01N41/06; A01N41/10; A01N43/10; A01N43/12; A01N43/40; A01N47/24; A01N47/34; C07C251/86; C07C251/88; C07C257/22; C07C259/20; C07C281/04; C07C281/14; C07C311/05; C07C311/46; C07C317/28; C07C317/32; C07C323/24; C07C323/35; C07C327/42; C07C329/00; C07C333/00; C07D213/87; C07D333/38; C07D333/70; (IPC1-7): C07C251/86; A01N35/10; A01N37/28; A01N43/10; A01N43/40; C07C251/88; C07C257/22; C07C259/20; C07C281/04; C07C281/14; C07C311/46; C07C317/28; C07C317/32; C07C323/24; C07C323/35; C07C327/42; C07C329/00; C07C333/00
Attorney, Agent or Firm:
Nobuo Kaida (1 person outside)