Abstract:
Moniklines, bei 147 - 148 °C schmelzendes 2-Chlor-N-(4’-chlorbiphenyl-2-yl)-nicotinamid der Formel (I) sowie ein Verfahren zu dessen Herstellung.
Abstract:
2-Mercapto-substituierte Triazolopyrimidine der Formel (I) in der die Substituenten folgende Bedeutung haben:L Halogen, Cyano, Nitro, Alkyl, Alkenyl, Alkinyl, Halogenalkyl, Halogenalkenyl, Alkoxy, Alkenyloxy, Alkinyloxy, Halogenalkoxy oder -C(=O)-A;A Wasserstoff, Hydroxy, Alkyl, Alkenyl, Alkoxy, Halogenalkoxy, Alkylamino oder Dialkylamino;m 0 oder 1, 2, 3, 4 oder 5;X Halogen, Cyano, Alkyl, Halogenalkyl, Alkoxy oder Halogenalkoxy;R1,R2 Wasserstoff, Alkyl, Halogenalkyl, Cycloalkyl, Halogencycloalkyl, Alkenyl, Alkadie-nyl, Halogenalkenyl, Cycloalkenyl, Alkinyl, Halogenalkinyl oder Cycloalkinyl, Phenyl, Naphthyl, oder ein fünf- bis zehngliedriger gesättigter, partiell ungesättig-ter oder aromatischer Heterocyclus, enthaltend ein bis vier Heteroatome aus der Gruppe O, N oder S, R1 und R2 können auch zusammen mit dem Stickstoffatom, an das sie gebunden sind, einen fünf- oder sechsgliedrigen Ring bilden, der durch ein Atom aus der Gruppe O, N und S unterbrochen sein;wobei R1 und/oder R2 gemäß der Beschreibung substituiert sein können;Verfahren zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Ver-wendung zur Bekämpfung von pflanzenpathogenen Schadpilzen.
Abstract:
Disclosed are fungicidal mixtures for controlling rice pathogens, containing a synergistically effective amount of 1) a compound of formula (I), and 2) a compound of formula (II) as active components, methods for controlling destructive fungi by means of mixtures of compound I and compound II, the use of compounds I and II for producing such mixtures, and agents containing said mixtures.
Abstract:
Substituted 6-(2-halogenphenyl)-triazolopyrimidines of formula (I) in which R1 denote alkyl, alkenyl, alkynyl, alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or a 5- or 6-membered saturated, unsaturated, or aromatic heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, wherein R 1 and R 2 radicals may be substituted as defined in the description, R 2 denote hydrogen, or a group mentioned for R 1 ; or R 1 and R 2 together with the interjacent nitrogen atom represent a 5- or 6-membered heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which ring may be substituted as defined in the description; Hal is halogen; L 1 , L 3 independently denote hydrogen, halogen, or alkyl; L 2 is hydrogen, halogen, haloalkyl, or NH 2 , NHR b , or N(Rb) 2 , wherein Rb is as defined in the description,wherein at least one from L 1 , L 2 , and L 3 is not hydrogen; X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
Abstract:
Substituted 6-(2-halogenphenyl)-triazolopyrimidines of formula (I) in which R1 denote alkyl, alkenyl, alkynyl, alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or a 5- or 6-membered saturated, unsaturated, or aromatic heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, wherein R and R radicals may be substituted as defined in the description, R denote hydrogen, or a group mentioned for R ; or R and R together with the interjacent nitrogen atom represent a 5- or 6-membered heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which ring may be substituted as defined in the description; Hal is halogen; L , L independently denote hydrogen, halogen, or alkyl; L is hydrogen, halogen, haloalkyl, or NH2, NHR , or N(Rb)2, wherein Rb is as defined in the description,wherein at least one from L , L , and L is not hydrogen; X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
Abstract translation:取代的式(I)的6-(2-卤代苯基) - 三唑并嘧啶,其中R1表示烷基,烯基,炔基,链二烯基,卤代烷基,卤代烯基,环烷基,苯基,萘基或5-或6-元饱和,不饱和或 芳族杂环,其含有1-4个氮原子或一至三个氮原子和一个硫或氧原子,其中R 1和R 2基团可以如说明书中所定义地被取代,R 2表示氢,或 R 1中提到的基团; 或R 1和R 2连同相邻的氮原子表示含有1-4个氮原子或1-3个氮原子和一个硫或氧原子的5-或6-元杂环,该环可以被取代 如说明书中所定义的; 卤素是卤素; L 1,L 3独立地表示氢,卤素或烷基; L 2是氢,卤素,卤代烷基或NH 2,NHR b或N(R b)2,其中R b如说明书中所定义,其中至少一个L 1,L 2, 而L 3不是氢; X是卤素,氰基,烷基,烷氧基,卤代烷氧基或烯氧基,它们的制备方法,含有它们的组合物和它们用于防治植物病原性真菌的用途。
Abstract:
Fungizide Mischungen, enthaltend A) die Verbindung der Formel (I) und B) die Verbindung der Formel (II) einer synergistisch wirksamen Menge, Verfahren zur Bekämpfung von Schadpilzen mit Mischungen der Verbindungen (I) und (II) un die Verwendung der Verbindungen (I) und (II) zur Herstellung derartiger Mischungen.
Abstract:
Die vorliegende Erfindung betrifft neue Phenethylacrylamide der Formel (I), in der die Substituenten R 1 , R 2 , R 3 und R 4 folgende Bedeutungen haben: R l Wasserstoff, Halogen, C 1 -C 4 -Alkyl, C 1 -C 4 -Alkoxy, C 3 -C 8 -Cycloalkyl, C 1 -C 4 -Halogenalkoxy oder C 1 -C 4 -Halogenalkyl; R 2 Wasserstoff, Halogen, C 1 -C 4 -Alkyl, C 1 -C 4 -Alkoxy, C 3 -C 10 -Cycloalkyl, C 1 -C 4 -Halogenalkoxy oder C 1 -C 4 -Halogenalkyl; R 3 C 1 -C 4 -Alkyl, C 1 -C 4 -Halogenalkyl, Propargyl, C 3 -C 4 -Alkenyl oder ein Rest der Formel -H 2 C-C=C-C(R a ,R b )-R c , worin R a , R b unabhängig voneinander Wasserstoff oder Methyl bedeuten und R c für Wasserstoff oder C 1 -C 4 -Alkyl steht; R 4 Methyl oder C 1 -Halogenalkyl; und Het für einen 5- oder 6-Ring Heteroaromaten steht, Verfahren zu deren Herstellung und die Verwendung von Phenethylacrylamiden der Formel (I) zur Bekämpfung von pflanzenpathogenen Schadpilzen.
Abstract:
Fungizide Mischung, enthaltend (1) 2-[2-(1-Chlorcyclopropyl)-3-(2-chlorphenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazol-3-thion (Prothioconazole) der Formel (I) oder dessen Salze oder Addukte und mindestens ein weiteres Triazol oder dessen Salze oder Addukte, ausgewählt aus Epoxiconazole, Metconazole, Propiconazole, Fluquinconazole, Penconazole, Difenconazole, Hexaconazole, Cyproconazole, Flusilazole, Tetraconazole, Fenbuconazole, Myclobutanil, Simeconazole, Ipconazole, Triticonazole in einer synergistisch wirksamen Menge.
Abstract:
Substituted 6-(2-tolyl)-triazolopyrimidines of formula (I) in which R 1 and R 2 independently denote hydrogen or alkyl, alkenyl, alkynyl, or alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R 1 and R 2 radicals may be unsubstituted or substituted as defined in the description, or R 1 and R 2 together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; R 3 is halogen, cyano, alkyl, alkoxy, haloalkyl, or C(=O)A, wherein A is hydrogen, hydroxy, alkyl, amino, or mono- or dialkyl-amino; n is an integer from 1 to 4; and X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
Abstract:
6-(2-Chloro-6-fluoro-phenyl)-triazolopyrimidines of formula (I), in which R 1 and R 2 independently denote hydrogen or alkyl, alkenyl, alkynyl, alkadienyl, or haloalkyl, cycloalkyl, bicycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R 1 and R 2 radicals may be unsubstituted or partially or fully halogenated or may be substituted as defined in the description, R 1 and R 2 together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; X is cyano, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.