52.
    发明专利
    未知

    公开(公告)号:DE2131401A1

    公开(公告)日:1972-12-28

    申请号:DE2131401

    申请日:1971-06-24

    Applicant: BASF AG

    Inventor: FISCHER ADOLF DR

    Abstract: 1385436 Mixed herbicides BADISCHE ANILIN-& SODA-FABRIK AG 22 June 1972 [24 June 1971] 29238/72 Heading A5E A herbicide comprises a mixture of a) a benzothiazinone-(4)-2, 2-dioxide compound of the formula: where R denotes alkyl of 1 to 4 carbon atoms, or a salt of the said compound and b) a substituted urea compound of the formula: where R denotes 3, 4-dichlorophenyl, 4-chlorophenyl, 4 - fluorophenyl, 3 - chloro - 4 - methylphenyl, 3-chloro-4-bromophenyl, 4-bromophenyl, 3-chloro-4-methoxyphenyl, 3-tert-butylcarbamoyloxyphenyl, 3-(N-vinyl-N-tert-butyl)- carbamoyloxyphenyl, 3-isopropylcarbamoyloxyphenyl, 3-trifluoromethylphenyl, phenyl or N- 2-benzothiazolyl, R 1 denotes hydrogen, cyclohexenyl, cyclooctenyl, CH 2 -O-C-alkyl or # O methyl, R 2 denotes hydrogen, methyl, methoxy, butyn-(1)-yl-(3) or chloroformyl and X denotes oxygen or sulfur. The salt of (a) may be an alkali or alkaline earth metal salt, an ammonium salt or an inorganic or organic amine salt. The composition finds application in combating weeds in cereal crops.

    1 subst 4 amino 6 pyridazones with herbicidal - activity

    公开(公告)号:DE1966311A1

    公开(公告)日:1972-03-23

    申请号:DE1966311

    申请日:1969-03-13

    Applicant: BASF AG

    Abstract: 1-Subst-4-amino-6-pyridazones with herbicidal activity Title cpds. are 1-R-4-X-5-Y-6-pyridazones where R is phenyl or aralkyl (opt. subst. by halogen, alkyl, alkoxy or haloalkyl) or cyclohexyl (opt. subst by halogen, or alkyl), Y is H, halogen, alkoxy or mercaptoalkyl and X is cyclopropanecarboxamido, (m-alkanoylaminophenoxy) carbonylamino, (m-alkoxycarbonylaminophenoxy)carbonylamino, N'-cycloalkyl-N'-hydroxy-ureido or N'-chlorosulphonyl-ureido; X can also be NH2 or acetamido when Y is H or is aralkyl. The cpds. may be prepd. by reacting corr. 4-isocyrindopyridazines with m-acylaminophenols or hydroxylamines, by reacting 4-aminopyridazones with chlorosulphonyl isocyanate or cyclopropanecarboxylic acid chloride, by reacting 4,5-dihalopyridazones with NH3, or by reacting 4-amino-5-chloropyridazones with hydrogen.

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