中科微点-全球专利检索

  1. Login
  2. Sign Up

Search Results

206 records (took 0.044 seconds)

    Fungicidní smesi
    94.
    发明专利
    Fungicidní smesi 未知

    公开(公告)号：CZ301674B6

    公开(公告)日：2010-05-19

    申请号：CZ20031953

    申请日：2002-01-17

    Applicant: BASF AG

    Inventor： EICKEN KARL ,  ROSE INGO ,  AMMERMANN EBERHARD ,  STIERL REINHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SCHERER MARIA ,  SCHELBERGER KLAUS ,  HADEN EGON ,  HAMPEL MANFRED

    IPC: A01N43/40 ,  C07C49/84 ,  A01N35/04 ,  A01N37/06 ,  A01N37/18 ,  C07C69/157

    Abstract: Fungicidní smesi, které se vyznacují tím, že sestávají z a) benzofenonu obecného vzorce I, ve kterém R.sup.1.n. je atom chloru, methylová skupina, methoxylová skupina, acetoxyskupina, pivaloyloxyskupina nebo hydroxylová skupina; R.sup.2.n. je atom chloru nebo methylová skupina; R.sup.3.n. je atom vodíku, atom halogenu nebo methylová skupina; a R.sup.4.n. je alkylová skupina s 1 až 6 atomy uhlíku nebo benzylová skupina, ve které fenylová cást benzylového zbytku muže nést atom halogenu nebo methylový substituent, a b) amidických sloucenin obecného vzorce II, ve kterém R.sup.6.n. a R.sup.7.n. jsou substituenty identické nebo ruzné, jako je atom halogenu, nitroskupina, kyanoskupina, alkylová skupina, alkenylová skupina, alkynylová skupina, halogenalkylová skupina, halogenalkenylová skupina, halogenalkynylová skupina, alkoxylová skupina, halogenalkoxylová skupina, alkylthio-skupina, halogenalkylthioskupina, alkylsulfinylová skupina nebo alkylsulfonylová skupina; X je 1, 2, 3 nebo 4; a y je 1, 2, 3, 4, nebo 5; v synergicky úcinném množství, metod pro kontrolu škodlivých plísní použitím smesí sloucenin vzorce I a vzorce II a prostredku, které je obsahují.

    98.
    发明专利
    未知

    公开(公告)号：DE50209496D1

    公开(公告)日：2007-03-29

    申请号：DE50209496

    申请日：2002-07-03

    Applicant: BASF AG

    Inventor： MUELLER BERND ,  SAUTER HUBERT ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  TORMO I BLASCO JORDI ,  GROTE THOMAS ,  GYPSER ANDREAS ,  RHEINHEIMER JOACHIM ,  ROSE INGO ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  RACK MICHAEL ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  AMMERMANN EBERHARD ,  STIERL REINHARD

    IPC: C07D487/04 ,  A01N43/90

    Abstract: 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines (I) are new. 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines of formula (I) are new. [Image] n : 0-5; R : halo, CN, OH or OCN, or alkyl, alkenyl, alkynyl, T', haloalkenyl, OT, alkenyloxy, alkynyloxy, OT', cycloalkyl, cycloalkenyl, cycloalkoxy, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, CONH 2, mono- or dialkylaminocarbonyl, alkoximinoalkyl, alkenyloximinocarbonyl, alkynyloximinoalkyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, cycloalkylcarbonyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); T : 1-6C alkyl; T' : 1-6C haloalkyl; Het : 5-10 membered, saturated, partially unsaturated or aromatic heterocycle containing 1-4 of O, N and/or S heteroatoms; R 11-10C alkyl, alkenyl, alkynyl, 3-12C cycloalkyl, 3-10C cycloalkenyl, phenyl, naphthyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); R ahalo, CN, NO 2, OH, T, T', COT, cycloalkyl, OT, OT', COOT, NHT, NT 2, 2-6C alkenyl, 2-6C alkenyloxy, 3-6C alkynyloxy, alkoximino, alkenyloximino, alkynyloximino, aralkoximino, alkynyl, alkynyloxycarbonyl, phenyl, naphthyl or Het (where all aliphatic, alicyclic or aromatic groups are optionally partially or completely halogenated and optionally substituted by 1-3 R aand/or 1-3 R c); R bhalo, CN, NO 2, OH, SH, NH 2, COOH, CONH 2, CSNH 2, T, T', 2-8C alkenyl, 2-8C alkenyloxy, 2-8C alkynyloxy, OT, OT', ST, NHT, NT 2, CHO, COT, SO 2T, SOT, COOT, OCOT, CONHT, CONT 2, CSNHT or CSNT 2; R ccycloalkyl, -O-cycloalkyl, heterocyclyl, -O-heterocyclyl, aryl, -O-aryl, -S-aryl, -O-T-aryl, -T-aryl, heteroaryl, -O-heteroaryl or -S-heteroaryl (where cycloalkyl or heterocyclyl rings are 3-10 membered, aryl rings are preferably 6-10 membered and heteroaryl rings are preferably 5-6 membered; and all rings are optionally partially or completely halogenated and optionally substituted by alkyl or haloalkyl); and R 21-4C alkyl, 2-4C alkynyl or 2-4C alkynyl (all optionally substituted by halo, CN, NO 2, OMe, OEt or 1-4C alkoxycarbonyl; Unless specified otherwise alkyl moieties have 1-8C, alkenyl or alkynyl moieties 2-10C and cycloalkyl or cycloalkenyl moieties 3-6C. Independent claims are also included for: (1) preparation of (I); and (2) dicarbonyl compound intermediates of formula (III), provided that n is not 0 and R 1and R 2are not both Me. [Image] ACTIVITY : Fungicide. 7-Cyclohexyl-5-methyl-6-(2-chloro-6-fluorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine (Ia) at a concentration of 63 ppm gave at least 90 % protection of tomato plants against Alternaria solani. MECHANISM OF ACTION : None given.

Patent Agency Ranking