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    Novel n-arylcarbamic acid esters
    1.
    发明授权
    Novel n-arylcarbamic acid esters 失效
    新型N-亚硝酸酸酯

    公开(公告)号：US3920727A

    公开(公告)日：1975-11-18

    申请号：US26590972

    申请日：1972-06-23

    Applicant: BAYER AG

    Inventor： METZGER CARL ,  JAGER GERHARD ,  LURSSEN KLAUS

    IPC: A01N47/20 ,  C07C271/06 ,  C07D307/88 ,  C07C125/06

    CPC classification number: C07D307/88 ,  A01N47/20 ,  C07C271/06

    Abstract: New N-arylcarbamic acid esters of the formula

    wherein R4 is hydrogen or is defined as R4 is defined above, and Y and Y'' are oxygen or sulfur, ARE OUTSTANDINGLY EFFECTIVE IN REGULATING THE GROWTH OF PLANTS, I.E., TO INHIBIT, STIMULATE OR ALTER THE GROWTH OF PLANTS.

    IN WHICH R is lower aliphatic hydrocarbyl, optionally substituted, R1, R2 and R3, which may be identical or different, are each hydrogen, alkyl, cycloalkyl, alkoxy, haloalkyl or halogen, R4 is alkyl, alkenyl, alkynyl, cycloalkenyl, haloalkyl, haloalkenyl, haloalkynyl, alkoxyalkyl or alkylthioalkyl, acylalkyl (i.e., alkanoyloxyalkyl), alkoxycarbonylalkyl, carbalkoxyalkyl, carbalkoxyalkenyl, or an optionally substituted cycloalkyl, aryl, aralkyl, aryloxyalkyl or arylthioalkyl radical, or the grouping

    Phenyl-imidazolyl-alkanyl derivatives, their production and use
    3.
    发明授权
    Phenyl-imidazolyl-alkanyl derivatives, their production and use 失效
    苯基 - 咪唑烷基 - 烷基衍生物，其生产和使用

    公开(公告)号：US3892764A

    公开(公告)日：1975-07-01

    申请号：US34693973

    申请日：1973-04-02

    Applicant: BAYER AG

    Inventor： METZGER CARL ,  MEISER WERNER ,  BUECHEL KARL HEINZ ,  PLEMPEL MANFRED

    IPC: C07D521/00 ,  C07D49/36

    CPC classification number: C07D231/12 ,  C07D233/56 ,  C07D249/08

    Abstract: Phenyl-imidazolylalkanyl derivatives are antimycotic agents. They are prepared by a number of processes including acylation or sulfonylation of a phenyl-imidazolylalkanol, treatment of a phenyl-alkanyl-carbinol with a diimidazolyl sulfone, oxidation of a phenyl-imidazolylalkylmercaptan or reduction of a phenylimidazolylalkanoate or alkanonitrile. A typical embodiment is 1(1,1-diphenyl-2-acetoxyethyl)imidazole.

    Abstract translation: 苯基 - 咪唑烷基烷基衍生物是抗真菌剂。 它们通过许多方法制备，包括苯基 - 咪唑基烷醇的酰化或磺酰化，用二咪唑基砜处理苯基 - 烷基 - 甲醇，氧化苯基 - 咪唑烷基硫醇或还原苯基 - 咪唑烷基链烷酸酯或链烷腈。 典型的实施方案是1-（1,1-二苯基-2-乙酰氧基乙基）咪唑。

    Carboxylic acid (1 2 4-thiadiazol-5-yl)-amides
    5.
    发明授权
    Carboxylic acid (1 2 4-thiadiazol-5-yl)-amides 失效
    羧酸（1 2 4 - 噻二唑-5-基） - 酰胺

    公开(公告)号：US3629275A

    公开(公告)日：1971-12-21

    申请号：US3629275D

    申请日：1968-08-29

    Applicant: BAYER AG

    Inventor： METZGER CARL ,  BORRMANN DIETER ,  WEGLER RICHARD ,  EUE LUDWIG ,  HACK HELMUTH

    IPC: C07D285/08

    CPC classification number: C07D285/08

    Abstract: ((ALKYL,HALOALKYL, ALKOXY AND PHENOXY)-CARBONYL)-N(3-ALKYL AND PHENYL-1,2,4-THIADIAZOL-5-YL)-AMIDES, I.E. (ALKANOYL, HALOALKANOYL, CARBOALKOXY AND CARBOPHENOXY)-N-(3-ALKYL AND PHENYL-1,2,4-THIADIAZOL-5-YL)-AMIDES OR (ALKANOIC, HALOAKANOIC, MONOALKYL CARBONIC AND MONOPHENYL CARBONIC ACID)-N-(3-ALKYL AND PHENYL-1,2,4THIADIAZOL-5-YL)-AMIDES, WHICH POSSESS HERBICIDAL PROPERTIES, AND WHICH MAY BE PRUCED BY CONVENTIONAL METHODS.

    1,2,4-thiodiazolyl-urea herbicidal agents
    6.
    发明授权
    1,2,4-thiodiazolyl-urea herbicidal agents 失效
    1,2,4-THIODIAZOLYL-UREA除草剂

    公开(公告)号：US3873299A

    公开(公告)日：1975-03-25

    申请号：US26348872

    申请日：1972-06-16

    Applicant: BAYER AG

    Inventor： METZGER CARL ,  BORRMANN DIETER ,  WEGLER RICHARD ,  EUE LUDWIG ,  HACK HELMUTH

    IPC: C07D285/08 ,  A01N9/12

    CPC classification number: C07D285/08

    Abstract: N-(3-(alkyl, alkylmercapto, dialkylamino and phenylsubstituted)-1,2,4-thiadiazol-5-yl)-N-(unsubstituted and alkylsubstituted)-N'',N''-(mono- and di- -alkyl-substituted) ureas which possess herbicidal properties, and which may be produced by conventional methods.

    Abstract translation: N- [3-（烷基，烷基巯基，二烷基氨基和苯基取代的）-1,2,4-噻二唑-5-基] -N- [未取代和烷基取代的] -N'，N' - [单 - 和 二烷基取代的]脲，其具有除草性，并且可以通过常规方法制备。

    Phenyl-imidazolyl acetic acid amino alkanol esters and amides
    7.
    发明授权
    Phenyl-imidazolyl acetic acid amino alkanol esters and amides 失效
    苯基咪唑啉酮酸性氨基酸烷基酯和氨基酸

    公开(公告)号：US3872117A

    公开(公告)日：1975-03-18

    申请号：US13928471

    申请日：1971-04-30

    Applicant: BAYER AG

    Inventor： MEISER WERNER ,  METZGER CARL ,  BUCHEL KARL HEINZ ,  PLEMPEL MANFRED

    IPC: C07D233/54 ,  C07D233/56 ,  C07D249/08 ,  C07D521/00 ,  C07D87/42

    CPC classification number: C07D231/12 ,  C07D233/56 ,  C07D249/08

    Abstract: Antimicrobial aminoalkyl phenyl-azolylalkanoates and N(aminoalkyl)phenyl-azolylalkanamides and salts thereof are prepared by treatment of the corresponding phenyl-halo-alkanoate or alkanamide with an azolyl compound or saalt thereof, treatment of the corresponding phenyl-hydroxyalkanoate or phenylhydroxyalkanamide with an azole compound under dehydration conditions or with a thionyl-bis-azole, or transesterification or amidation of a (lower)alkyl phenyl-azolylalkanoate. A typical embodiment is diphenyl-imidazolyl-acetic acid 1-dimethylamino-2propyl ester.

    Abstract translation: 通过用唑基化合物或其盐处理相应的苯基 - 卤代 - 链烷酸酯或烷酰胺，处理相应的苯基 - 羟基链烷酸酯或苯基 - 羟基链烷酰胺来制备抗微生物氨基烷基苯基 - 唑基烷酰胺和N-（氨基烷基）苯基 - 唑基烷酰胺及其盐 在脱水条件下或与亚硫酰基 - 双 - 唑的唑化合物，或（低级）烷基苯基 - 唑基烷酸酯的酯交换或酰胺化。 典型的实施方案是二苯基 - 咪唑基 - 乙酸1-二甲基氨基-2-丙基酯。

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