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公开(公告)号:DE3824210A1
公开(公告)日:1990-01-18
申请号:DE3824210
申请日:1988-07-16
Applicant: BASF AG
Inventor: LEYENDECKER JOACHIM DR , THEOBALD HANS DR , BUERSTINGHAUS RAINER DR , KUENAST CHRISTOPH DR , HOFMEISTER PETER DR
IPC: C07D237/18 , A01N43/58 , A01N43/80 , C07D413/12
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公开(公告)号:DE3714709A1
公开(公告)日:1988-11-17
申请号:DE3714709
申请日:1987-05-02
Applicant: BASF AG
Inventor: BUERSTINGHAUS RAINER DR , NEUBAUER HANS-JUERGEN DR , HOFMEISTER PETER DR , KUENAST CHRISTOPH DR
IPC: A01N43/50 , A01N43/52 , A01N43/56 , A01N43/653 , C07D231/56 , C07D233/60 , C07D233/68 , C07D235/06 , C07D235/08 , C07D249/10 , C07D521/00
Abstract: N-Substituted imidazoles of the general formula I in which the substituents have the following meanings: R and R denote hydrogen, halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl or nitro, R denotes hydrogen or halogen, R and R denote hydrogen, chlorine or methyl and X denotes -CH20- or -O(CH2)n-, where n is an integer from 1 to 3, their preparation and their use for controlling pests.
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公开(公告)号:DE3713337A1
公开(公告)日:1988-11-10
申请号:DE3713337
申请日:1987-04-21
Applicant: BASF AG
Inventor: THEOBALD HANS DR , KUENAST CHRISTOPH DR , HOFMEISTER PETER DR , NEUBAUER HANS-JUERGEN DR , KUEKENHOEHNER THOMAS DR , KRIEG WOLFGANG DR
IPC: C07D231/12 , C07D233/28 , C07D233/54 , C07D249/08 , C07D261/08 , C07D261/10 , C07D261/12 , C07D271/06 , C07D271/10 , C07D275/02 , C07D277/24 , C07D307/42 , C07D333/16 , A01N43/80
Abstract: [(p-Phenoxy)phenoxy]methylisoxazoles of the general formula I in which R , R and R are hydrogen, halogen, C1-C8-alkyl, C1-C8-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, nitro or cyano, R is hydrogen or C1-C4-alkyl, R is hydrogen, halogen, C1-C8-alkyl or C2-C8-alkenyl, R is hydrogen, C1-C8-alkyl, C2-C8-alkenyl, C1-C4-haloalkyl, C2-C8-alkoxyalkyl, C3-C10-cycloalkyl, aryl, C7-C20-arylalkyl, or is aryl or C7-C20-arylalkyl, each of which is mono- to trisubstituted in the aryl moiety by halogen, C1-C8-alkyl, C1-C8-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy or cyano or mono- to disubstituted by nitro, and processes for their preparation and their use for controlling pests.
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公开(公告)号:DE3711268A1
公开(公告)日:1988-10-13
申请号:DE3711268
申请日:1987-04-03
Applicant: BASF AG
Inventor: NEUBAUER HANS-JUERGEN DR , BUERSTINGHAUS RAINER DR , KUENAST CHRISTOPH DR , HOFMEISTER PETER DR
IPC: C07C313/00 , A01N39/00 , A01N53/00 , A01N53/12 , C07C67/00 , C07C231/00 , C07C231/02 , C07C233/57 , C07C233/60 , C07C323/18 , C07C323/20 , C07C103/737 , C07C149/32
Abstract: Cyclopropanecarboxamides of the general formula I (I) where R is C1-C12-alkyl, C2-C12-alkenyl, C2-C12-alkynyl, C1-C12-haloalkyl, C2-C12-haloalkenyl, C2-C12-haloalkynyl, C3-C12-alkoxyalkyl, C3-C8-cycloalkyl, C4-C12-cycloalkylalkyl, C3-C8-halocycloalkyl, C4-C12-halocycloalkylalhaloalkyl C4-C12-cycloalkylhaloalkyl or C4-C12-halocycloalkylhaloalkyl and X is oxygen or sulfur. The present invention furthermore relates to the preparation of the compounds I, pesticides which contain the compounds I, and a method for controlling pests.
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公开(公告)号:DE3529126A1
公开(公告)日:1987-02-19
申请号:DE3529126
申请日:1985-08-14
Applicant: BASF AG
Inventor: BUERSTINGHAUS RAINER DR , HOFMEISTER PETER DR , NEUBAUER HANS-JUERGEN DR , SEPPELT WOLFGANG DR , HAMPRECHT GERHARD DR , LIESE THOMAS DR , ADOLPHI HEINRICH DR , KUENAST CHRISTOPH DR
IPC: A01N37/10 , A01N37/34 , A01N37/40 , A01N37/48 , A01N43/24 , A01N43/30 , C07C69/78 , C07C69/86 , C07C69/92 , C07C205/38 , C07C205/57 , C07C205/58 , C07C205/59 , C07D317/46 , C07D317/48 , C07D317/64 , C07D319/20 , C07C79/46 , C07C149/40
Abstract: Benzoic esters of the formula I in which R , R , R , R and R have the meaning given in the description, their preparation, and their use in pest control.
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公开(公告)号:CZ293591B6
公开(公告)日:2004-06-16
申请号:CS287291
申请日:1991-09-20
Applicant: BASF AG
Inventor: BRAND SIEGBERT DR , AMMERMANN EBERHARD DR , SEUTER HUBERT DR , OBERDORF KLAUS DR , KARDORFF UWE DR , KUENAST CHRISTOPH DR , LORENZ GISELA DR
IPC: A01N35/10 , A01N37/18 , A01N37/50 , A01N43/08 , A01N43/40 , A01N43/60 , A01N43/78 , A01N53/10 , C07C235/06 , C07C235/34 , C07C235/46 , C07C235/78 , C07C245/08 , C07C251/48 , C07C255/57 , C07C255/61 , C07C255/62 , C07C255/64 , C07C309/66 , C07C309/73 , C07C309/76 , C07C323/18 , C07C323/20 , C07C323/47 , C07C323/56 , C07C323/60 , C07C323/62 , C07C323/63 , C07D213/30 , C07D213/53 , C07D213/56 , C07D213/61 , C07D213/64 , C07D213/643 , C07D213/70 , C07D215/14 , C07D215/22 , C07D215/227 , C07D277/64 , C07D277/68 , C07D277/74 , C07D307/42 , C07D307/52
Abstract: In the present invention, there are disclosed ortho-substituted phenylacetic acid amides of the general formula I, in which W represents an alkoxyimino, alkoxymethylene or alkylthiomethylene group containing 1 to 4 carbon atoms in the alkyl moiety. There are described fungicidal agents containing a liquid or solid carrier substance and at least one amide of the general formula I and process for preparing the amide, wherein the corresponding phenyl acetonitrile derivative of the general formula IV is subjected to hydrolysis in the presence of a base or an acid and subsequently it is subjected on the amide nitrogen to mono- or bisalkylation with alkyl halide. Described are also phenyl acetonitrile derivatives of the general formula IV.
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公开(公告)号:CZ287402B6
公开(公告)日:2000-11-15
申请号:CS196691
申请日:1991-06-27
Applicant: BASF AG
Inventor: BRAND SIEGBERT DR , KARDORFF UWE DR , KIRSTGEN REINHARD , MUELLER BERND DR , OBERDORF KLAUS DR , SAUTER HUBERT DR , LORENZ GIZELA DR , AMMERMANN EBERHARD DR , KUENAST CHRISTOPH DR , HARREUS ALBRECHT DR
IPC: C07C251/60 , A01N37/32 , A01N37/34 , A01N37/36 , A01N37/38 , A01N37/42 , A01N37/44 , A01N37/50 , A01N37/52 , A01N43/00 , A01N43/16 , C07C255/64 , C07C257/06 , C07C323/47 , C07C323/50 , C07C323/56 , C07C323/60 , C07C327/22 , C07D209/48 , C07D309/04 , C07D309/12 , C07D309/28 , C07D401/04 , C07D401/12
Abstract: N-Phthaloyl-O-benzyl oxime ethers (I) are new. X = CH2, CH(1-4C alkyl), CH(1-4C alkoxy), CH(1-4C alkylthio or N(1-4C alkoxy); Y = O, S or NR4; Z1, Z2 = H, halogen, methyl, methoxy or cyano; R1, R2, R4 = H or 1-4C alkyl; R3 = H, halogen, cyano, nitro or opt. substd. 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl, 1-4C haloalkoxy, aryl, aryloxy, benzyloxy, heteroaryl or heteroaryloxy; n = 1-4.
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公开(公告)号:AT161007T
公开(公告)日:1997-12-15
申请号:AT91109684
申请日:1991-06-13
Applicant: BASF AG
Inventor: BRAND SIEGBERT DR , KARDORFF UWE DR , KIRSTGEN REINHARD DR , MUELLER BERND DR , OBERDORF KLAUS DR , SAUTER HUBERT DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR , KUENAST CHRISTOPH DR , HARREUS ALBRECHT DR
IPC: C07C251/60 , A01N37/32 , A01N37/34 , A01N37/36 , A01N37/38 , A01N37/42 , A01N37/44 , A01N37/50 , A01N37/52 , A01N43/00 , A01N43/16 , C07C255/64 , C07C257/06 , C07C323/47 , C07C323/50 , C07C323/56 , C07C323/60 , C07C327/22 , C07D209/48 , C07D309/04 , C07D309/12 , C07D309/28 , C07D401/04 , C07D401/12
Abstract: N-Phthaloyl-O-benzyl oxime ethers (I) are new. X = CH2, CH(1-4C alkyl), CH(1-4C alkoxy), CH(1-4C alkylthio or N(1-4C alkoxy); Y = O, S or NR4; Z1, Z2 = H, halogen, methyl, methoxy or cyano; R1, R2, R4 = H or 1-4C alkyl; R3 = H, halogen, cyano, nitro or opt. substd. 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl, 1-4C haloalkoxy, aryl, aryloxy, benzyloxy, heteroaryl or heteroaryloxy; n = 1-4.
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公开(公告)号:DE59108746D1
公开(公告)日:1997-07-17
申请号:DE59108746
申请日:1991-07-20
Applicant: BASF AG
Inventor: RENTZEA COSTIN DR , KARDORFF UWE DR , KUENAST CHRISTOPH DR , THEOBALD HANS DR , KUEKENHOENER THOMAS DR
IPC: A01N43/10 , A01N43/78 , C07D277/22 , C07D277/24 , C07D333/08 , C07D333/12 , C07D333/16 , C07D333/24 , C07D333/28
Abstract: Acetylene derivatives of the formula I R -C IDENTICAL C-R I in which the substituents have the following meanings: R is an optionally substituted five-membered heteroaromatic, R is an optionally substituted aromatic ring system containing one to three rings, their preparation, agents containing them for controlling insects and acarids, and their use.
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公开(公告)号:DE19530175A1
公开(公告)日:1997-02-20
申请号:DE19530175
申请日:1995-08-17
Applicant: BASF AG
Inventor: DOHMEN GERHARD PETER DR , KUENAST CHRISTOPH DR , MUNK REINHART DR , ROTHHAAS GERHARD
Abstract: A method for combatting fish mycoses and one-celled ectoparasites on fish is characterized by the use of an active substance suited to inhibiting the mitochondrial respiratory chain at the point of the b/c1 complex.
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