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公开(公告)号:DE19609618A1
公开(公告)日:1997-09-18
申请号:DE19609618
申请日:1996-03-12
Applicant: BASF AG
Inventor: OBERDORF KLAUS DR , GRAMMENOS WASSILIOS DR , SAUTER HUBERT DR , GROTE THOMAS DR , MUELLER BERND DR , KIRSTGEN REINHARD DR , BAYER HERBERT DR , PTOCK ARNE DR , RACK MICHAEL DR , HARREUS ALBRECHT DR , ROEHL FRANZ DR , AMMERMANN EBERHARD DR , HARRIES VOLKER DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR
IPC: C07D239/32 , A01N43/54 , C07D239/34 , C07D239/36 , C07D405/04 , C07F7/22
Abstract: Pyrimidyl phenyl and benzyl ethers of general formula (I) and their salts and N oxides, in which the constituents and indices have the meanings: Q is C(CO2CH3)=CHCH3, C(CO2CH3)=CHOCH3, C(CONHCH3)=CHOCH3, C(CONH2)=NOCH3, C(CONHCH3)=NOCH3 or N(OCH3)-CO2CH3; n is 0 or 1; R is hydrogen or an organic radical bonded via a carbon atom; R is hydrogen, cyano, halogen or an organic radical bonded via a carbon, oxygen, sulphur or nitrogen atom; R is hydrogen, halogen, C1-C4 alkyl or C1-C2 alkyl halide; R is hydrogen, cyano, nitro, halogen or an organic radical bonded via a carbon, oxygen, sulphur or nitrogen atom; y is 0, 1, 2 or 3, where the radicals R may be different if y is 2 or 3; R is cyano, halogen, C1-C4 alkyl, C1-C4 alkyl halide or C1-C4 alkoxy; process and intermediate products for their production and their use as herbicide.
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公开(公告)号:AP2063A
公开(公告)日:2009-10-29
申请号:AP2005003456
申请日:2004-05-18
Applicant: BASF AG
Inventor: BLASCO TORMO I JORDI DR , GROTE THOMAS DR , SCHERER MARIA
Abstract: Fungicidal mixtures for controlling rice pathogens, comprising, as active components, 1) azoxystrobin of the formula I, and 2) the compound of the formula II, in a synergistically effective amount, methods for controlling harmful fungi using mixtures of the compound I with the compound II, the use of the compounds I and II for preparing such mixtures and compositions comprising these mixtures are described.
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公开(公告)号:AP200603778A0
公开(公告)日:2006-10-31
申请号:AP200603778
申请日:2005-03-08
Applicant: BASF AG
Inventor: BLASCO TORMO I JORDI DR , BLETTNER CARSTEN DR , MUELLER BERND DR , GEWEHR MARKUS DR , GRAMMENOS WASSILIOS DR , GROTE THOMAS DR , RHEINHEIMER JOACHIM DR , SCHAEFER PETER DR , SCHIEWECK FRANK DR , SCHWOEGLER ANJA DR , WAGNER OLIVER
IPC: A01N43/90 , C07D487/04
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公开(公告)号:AP200603696A0
公开(公告)日:2006-08-31
申请号:AP200603696
申请日:2005-01-14
Applicant: BASF AG
Inventor: GROTE THOMAS DR , BLASCO TORMO I JORDI DR , SCHERER MARIA , STIERL REINHARD DR , STRATHMANN SIEGFRIED DR , SCHOFL ULRICH DR
IPC: A01N43/90
CPC classification number: A01N43/90 , A01N43/88 , A01N2300/00
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公开(公告)号:AP2006003614A0
公开(公告)日:2006-06-30
申请号:AP2006003614
申请日:2004-11-05
Applicant: BASF AG
Inventor: GROTE THOMAS DR , SCHERER MARIA , STIERL REINHARD DR
IPC: A01N43/90
Abstract: Fungicidal mixtures for controlling rice pathogens, which mixtures comprise, as active components, 1) the triazolopyrimidine derivative of the formula I, and 2) propiconazole of the formula II, in a synergistically effective amount, methods for controlling rice pathogens using mixtures of the compound I with the compound II, the use of the compound I with the compound II for preparing such mixtures and compositions comprising these mixtures are described.
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公开(公告)号:CZ293561B6
公开(公告)日:2004-06-16
申请号:CZ124398
申请日:1996-10-11
Applicant: BASF AG
Inventor: GROTE THOMAS DR , BAYER HERBERT DR , MULLER RUTH DR , SAUTER HUBERT DR , KIRSTGEN REINHARD DR , HARRIES VOLKER DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR , STRATHMANN SIEGFRIED DR
IPC: C07C249/04 , A01N35/10 , A01N37/36 , A01N37/50 , C07C20060101 , C07C251/34 , C07C251/50 , C07C251/60 , C07C251/62 , C07C255/62 , C07C255/64 , C07C259/04 , C07C259/12 , C07C317/16 , C07C317/26 , C07C323/10 , C07C323/47 , C07C327/38 , C07C327/58 , C07C381/00
Abstract: In the present invention, there are described phenylacetic acid derivatives of the general formula I, processes for preparing these compounds, intermediates of the general formulae III and III' for preparing these compounds, whereby the substituents in the general formulae I, III and III' have specific meanings, further agents containing the above-indicated compounds, method of suppressing animal pest or harmful fungi using effective amount of the above compounds, as well as use of the above compounds for the preparation of an agent against animal pest and harmful fungi and for suppressing the animal pest or harmful fungi.
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公开(公告)号:AT265414T
公开(公告)日:2004-05-15
申请号:AT02023344
申请日:2002-10-18
Applicant: BASF AG
Inventor: ROSE INGO DR , TORMO I BLASCO JORDI DR , GEWEHR MARKUS DR , GRAMMENOS WASSILIOS DR , MUELLER BERND DR , RHEINHEIMER JOACHIM DR , SCHAEFER PETER DR , SCHIEWECK FRANK DR , GROTE THOMAS DR , GYPSER ANDREAS DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , STIERL REINHARD DR , STRATHMANN SIEGFRIED DR , CARTER PAUL DR , CURTZE JUERGEN DR
IPC: A01N31/14 , A01N31/16 , A01N33/10 , A01N37/38 , A01N37/40 , C07B61/00 , C07C39/42 , C07C41/26 , C07C43/23 , C07C69/017 , C07C69/14 , C07C323/19 , C07C323/25
Abstract: Polysubstituted 4-methoxy-benzhydryl alcohol or thiol derivatives (I) are new. Polysubstituted 4-methoxy-benzhydryl alcohol or thiol derivatives of formula (I) are new: X = O or S; R , R = halo, CN, NO2, OH, SH, NH2, alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, alkylcarbonyloxy, OCHO, alkylthio, alkenylthio, alkynylthio, mono- or dialkylamino, alkylcarbonyl or CHO (where all hydrocarbyl moieties are optionally mono- or polyhalogenated); R = halo, CN, NO2, OH, SH, NH2, alkyl, alkoxy, haloalkyl or haloalkoxy; R = alkyl, alkenyl or alkynyl (all optionally mono- or polyhalogenated); R , R = OH, alkyl, alkenyl, haloalkyl, haloalkenyl, alkoxy, alkenyloxy, haloalkoxy, haloalkenyloxy, cycloalkyl, cycloalkyl-(1-3C) alkyl, cycloalkoxy or cycloalkyl-(1-3C) alkoxy; and n = 0-2. Unless specified otherwise alkyl moieties have 1-6C, alkenyl or alkynyl moieties 2-6C and cycloalkyl moieties 3-8C. An Independent claim is also included for the preparation of (I).
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公开(公告)号:CZ290963B6
公开(公告)日:2002-11-13
申请号:CZ168698
申请日:1996-12-11
Applicant: BASF AG
Inventor: OBERDORF KLAUS DR , GRAMMENOS WASSILIOS DR , SAUTER HUBERT DR , GROTE THOMAS DR , KIRSTGEN REINHARD DR , MULLER RUTH DR , MULLER BERND DR , ROHL FRANZ DR , RACK MICHAEL DR , BAYER HERBERT DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR , STRATHMANN SIEGFRIED DR , HARRIES VOLKER DR
IPC: C07D239/26 , A01N43/54 , A01N47/20 , A01N47/24 , A01P3/00 , C07D239/28 , C07D239/34 , C07D239/38
Abstract: In the present invention there is disclosed a 2-O-[(pyrimidin-4-yl)methylenoxy]phenylacetic acid derivative of the general formula I, in which Re1 represents hydrogen or alkyl containing 1 to 4 carbon atoms, Re2 represents a halogen, alkyl having 1 or 2 carbon atoms or a haloalkyl with 1 to 2 carbon atoms in the alkyl moiety, Re3 represents hydrogen, amino, OH, mercapto, a halogen, alkyl containing 1 to 8 carbon atoms being optionally substituted with phenyl, which itself can be optionally substituted with 1 or 2 substituents that are independent on each other and that are selected from the group comprising a halogen, CN, NOi2, alkyl containing 1 to 4 carbon atoms, haloalkyl containing 1 to 4 carbon atoms, haloalkoxy containing 1 to 4 carbon atoms or Re3 represents a haloalkyl containing 1 to 8 carbon atoms and alkoxyalkyl having 1 to 8 carbon atoms in the alkoxy and 1 to 4 carbon atoms in the alkyl moiety, alkoxy containing 1 to 8 carbon atoms, monoalkylamino containing 1 to 8 carbon atoms in the monoalkyl moiety, dialkylamino having 1 to 8 carbon atoms in the dialkyl moiety, alkylthio containing 1 to 8 carbon atoms, alkylsulfoxyl with 1 to 8 carbon atoms, alkylsulfonyl containing 1 to 8 carbon atoms, cycloalkyl having 3 to 8 carbon atoms, trialkylsilyloxy with 1 to 8 carbon atoms in the alkyl moiety, or phenyl, phenoxy, phenoxymethyl, benzyloxy or heteroaryl being optionally substituted in the aromatic ring, Re4 represents hydrogen, CN, a halogen, alkyl containing 1 to 4 carbon atoms, haloalkyl with 1 to 4 carbon atoms in the alkyl moiety or alkoxy containing 1 to 4 carbon atoms, Q represents the group {C(=NOCHi3)-CONHCHi3}, {C(=NOCHi3)-COOCHi3} or {N(OCHi3)-COOCHi3}. The invented derivative or salt and N-oxides thereof are effective compounds used for fighting fungal and animal pest.
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公开(公告)号:DE19747788A1
公开(公告)日:1999-05-06
申请号:DE19747788
申请日:1997-10-29
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS DR , OBERDORF KLAUS DR , SAUTER HUBERT DR , GYPSER ANDREAS DR , BAYER HERBERT DR , GEWEHR MARKUS DR , GROTE THOMAS DR , MUELLER BERND DR , PTOCK ARNE DR , ROEHL FRANZ DR , HAMPRECHT GERHARDT DR , GOETZ NORBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR
IPC: A01N43/40 , C07D213/64 , C07D213/63
Abstract: The invention relates to substituted 2-(2'-pyridyloxy)phenyl acetamides of formula (I), in which the substituents have the following meaning: R = fluorine, chlorine, CH3 or halomethane; R = fluorine, bromine, alkyl or halomethane; R = hydrogen or one of the radicals cited in R and additionally R = 6-chlorine when R stands for hydrogen, R = 5-chlorine when R stands for fluorine, and the compound in which R , R and R stand for chlorine, whereby R cannot stand for chlorine when R stands for 5- trifluoromethyl and R represents hydrogen. The invention further relates to the methods for the production and the use thereof to combat fungi and animal pests.
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公开(公告)号:DE19745650A1
公开(公告)日:1999-04-22
申请号:DE19745650
申请日:1997-10-16
Applicant: BASF AG
Inventor: BAYER HERBERT DR , GEWEHR MARKUS DR , GROTE THOMAS DR , MUELLER BERND DR , SAUTER HUBERT DR , GRAMMENOS WASSILIOS DR , GYPSER ANDREAS DR , PTOCK ARNE DR , GOETZ ROLAND DR , RACK MICHAEL DR , AMMERMANN EBERHARD DR , HARRIES VOLKER DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR , ROEHL FRANZ DR
IPC: A01N43/82 , A01N43/836 , C07C259/14 , C07C265/12 , C07D271/06 , C07D271/07 , C07D413/12 , C07C251/40 , C07D413/04 , C07D413/14
Abstract: Substituted oxy- or oxymethylenephenyl-oxazolidine and -oxazolidinedione derivatives (I) are new. They are prepared from new activated phenyl-oxazolidine derivatives (IIA) and activated phenyl-oxazolidinedione derivatives (IVB), which in turn are obtained via new substituted nitrobenzene and aniline derivatives (1), phenyl isocyanates (2) and substituted anilides (3). Substituted oxy- or oxymethylenephenyl-oxazolidine and -oxazolidinedione derivatives (I) are new: Y = halo; 1-4C alkyl; 1-4C haloalkyl; or 1-4C alkoxy; n = 0-2; E = group of formula (a) or (b): Ra = halo; CN; 1-4C alkyl or 1-4C alkoxy optionally substituted by halo; 3-6C alkenyloxy, 3-6C alkynyloxy; 3-6C cycloalkyl; S(O)m-1-4C alkyl; or NRaRb; m = 0-2; Ra and Rb = H; 1-4C alkyl; 3-6C alkenyl; or 3-6C alkynyl; Rb = 1-4C alkyl; 1-4C haloalkyl; 3-6C cycloalkyl; or optionally substituted arylmethylene; T = O or oxymethylene; Z' = X; N=CWR ; or N=C(R )-C(R )=NOR ; X = optionally substituted heterocyclyl, aryl, heteroaryl, arylmethylene or heteroarylmethylene; W = optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heterocyclyl, aryl or heteroaryl; R = H; CN; 1-4C alkyl; 1-4C haloalkyl; 1-4C alkoxy; 1-4C alkoxy-1-4C alkyl; or 3-6C cycloalkyl; R = H; CN; halo; C(Rd)=NOR3; W; OW; SW or NRcW; Rc = H; alk yl; alkenyl; or alkynyl; Rd = H or alkyl; R = H; or optionally substituted alkyl, alkenyl or alkynyl. Independent claims are also included for: (A) activated phenyl-oxazolidine derivatives of formula (IIA); (B) activated phenyl-oxazolidinedione derivatives of formula (IVB); (C) substituted nitrobenzene and aniline derivatives of formula (1); (D) phenyl isocyanates of formula (2); and (E) Substituted anilides (3). L = OH; CH3; CH2L'; or L'; L' = nucleophilic leaving group; La = CH3; CH2L'; NO2; alkylsulphonate; or arylsulphonate; Q = NH2 or NO2; T' = OZ'; CH2O-X; or CH2O-N=C(R )-C(R )=NOR ; Z' = N=CWR or N=C(R )-C(R )=NOR ; E asterisk = NH-C(O)-NH-OH; NH-C(O)-O-NH-C(O)-OR; NH-C(S)-R'; or NH-C(NOH)-R'; R = 1-4C alkyl; R' = 1-4C alkyl; 1-4C haloalkyl; or 3-6C cycloalkyl.
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