Abstract:
A NOVEL COMPOUND OF THE GENERAL FORMULA,
(R2-Y-CH2-N(-R1)-CH=N-),(X)N-BENZENE
WHEREIN X IS A HALOGEN ATOM, OR AN ALKYL, HALOALKYL, ALKOXY, NITRO OR ALKYLCARBAMOYLOXY GROUP; N IS ZERO OR AN INTEGER OF 1 TO 3; R1 IS A HYDROGEN ATOM, OR AN ALKYL, ALKENYL, ALKYNYL, HALOALKYL, ALKYLTHIOALKYL, ALKOXYALKYL, HALOALKOXYALKYL OR HALOALKYLTHIOALKYL GROUP; R2 IS AN ALKYL, ALKENYL, ALKYNYL, ALKYLTHIOALKYL, ALKOXYALKYL OR HALOALKYL GROUP; Y IS AN OXYGEN OR SULFUR ATOM, IS USEFUL IN AGRICULTURE AND HORTICULTURE AS AN INSECTICIDAL AND MITICIDAL CHEMICAL CAPABLE OF EFFECTIVELY KILLING RICE BORERS WHICH ARE MOST INJURIOUS TO RICE AND SPIDER MITES WHICH ARE INJURIOUS TO FRUITS AND VEGETABLES, WITHOUT GIVING ANY PHYTOTOXICITY TO VARIOUS CULTIVATED CROPS SUCH AS, FOR EXAMPLE, RADISH, MELON, KIDNEY BEAN, TOMATO, STRAWBERRY, MANDARIN, PEAR, APPLE, GRAPE, CHRYSANTHEMUM AND TOBACCO. THE COMPOUND OF THE GENERAL FORMULA (I) IS PREPARED BY REACTING A COMPOUND OF THE GENERAL FORMULA,
(X)N-ANILINE
WHEREIN X AND N ARE AS DEFINED ABOVE, OR A SALT THEREOF, WITH A COMPOUND OF THE FORMULA
R2-Y-CH2-N(-R1)-CHO
WHEREIN R1, R2 AND Y ARE AS DEFINED ABOVE, AND WITH A HALOGENATING AGENT.
WHEREIN X AND Y ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE, BROMINE, LOWER ALKOXY, LOWER ALKYL, NO2 AND CF3, Z IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE, BROMINE, LOWER ALKOXY, LOWER ALKYL AND NO2, X'' IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE, BROMINE BENZYLOXY, NO2, SCN, CF3, LOWER ALKYL AND LOWER ALKOXY, Y'' IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE BROMINE, -NO2, CF3 AND LOWER ALKYL, Z IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE, BROMINE AND LOWER ALKYL, R AND R1 MAY BE DIFFERENT AND ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, LOWER ALKYL, BENZYL, CYCLOALKYL OF 3 TO 8 CARBON ATOMS, FURFURYL AND ARYL OPTIONALLY SUBSTITUTED WITH A MEMBER OF THE GROUP CONSISTING OF CHLORINE, BORMINE AND LOWER ALKOXY AND TAKEN TOGETHER WITH THE NITROGEN ATOM TO WHICH THEY ARE ATTAFCHED FROM A 5 TO 7 RING MEMBER HETEROCYCLIC WITH THE PROVISO THAT AT LEAST ONE OF X, Y, Z, R, R1, X'', Y'' AND Z'' IS OTHER THAN HYDROGEN WHICH HAVE REMARKABLE FUNGICIDAL ACTIVITY, THEIR PREPARATION AND NOVEL INTERMEDIATES THEREFORE.
Abstract:
BIS-GUANIDIUM TETRACHLOROPHTHALATES AND BIS-GUANIDIUM TETRABROMOPTHALATES AND PROCESS FOR OBTAINING SAME BY INTERACTION OF AN INORGANIC ACID SALT GUANIDINE AND TETRACHLOROPHTHALIC ANHYDRIDE OR TETRABROMOPHTHALIC ANHYDRIDE OR AN ALKALI METAL SALT OF TETRACHLOROPHTHALATE OR TETRABROMOPHTHALATE.
WHEREIN R IS A RADICAL HAVING FROM 1 TO 30 CARBON ATOMS, OF THE GROUP CONSISTING OF ALKYL, ARYL, POLYHALOALKYL, POLYHALOARYL, ALKARYL, ARALKYL, POLYHALOALKARYL, POLYHALOARALKYL, AND HETEROCYCLIC RADICALS WHICH ARE FREE FROM FUNCTIONAL GROUPS WHICH REACT WITH THE TRIFLUOROFORMAMIDINO GROUP, AND X IS A DIVALENT LINKING RADICAL OF THE GROUP CONSISTING OF
-O-, -NH-, -N(-R)-, -CH=N-, -S-, -CH=N-O-, AND -O-
Abstract:
N-Halo-N-Phenyl-N''N''dimethylformamidinium halides characterized by the following structural formula:
WHEREIN R is selected from the group consisting of hydrogen, C1C6 alkoxy, C1-C6 alkylthio, C1-C6 alkyl, bromine and chlorine; n is an integer ranging from 1 to 4; X is one selected from the group consisting of bromine and chlorine. These compounds possess pesticidal activity and show especially good fungicidal activity.
Abstract:
ANTIFUNGAL COMPOSITIONS ARE DISCLOSED WHICH CONTAIN AS ACTIVE INGREDIENTS AMIDINES OF THE FORMULA
R2-N=C(-R1)-N(-R3)-R4
WHEREIN
R1, R2, R3 AND R4 REPRESENT CERTAIN ORGANIC SUBSTITUENTS, OR SALTS OF SUCH AMIDINES WITH INORGANIC OR ORGANIC ACIDS; THESE COMPOSITIONS ARE PARTICULARLY USEFUL FOR THE PROTECTION OF PLANTS AGAINST PHYTOPATHOGENIC FUNGI; AND ALSO FOR COMBATING ACARINAE SUCH AS TICKS. METHODS FOR CONTROLLING SUCH FUNGI ON THE ONE HAND, AND ACARINAE, ON THE OTHER HAND, WITH THE AID OF THE AFORESAID AMIDINE DERIVATIVES ARE ALSO DESCRIBED. FURTHERMORE CERTAIN ISOBUTANE, ISOPENTANE AND PHENYLETHANE AMIDNES FALLING UNDER THE ABOVE FORMULA ARE DISCLOSED AS NOVEL COMPOUNDS.
Abstract:
THE PREPARATION AND ANTHELMINTIC PROPERTIES OF CERTAIN W-(3-R-O-PHENYL) SUBSTITUTED CYCLIC AND ACYCLIC AMIDINES; NAMELY, 1,4,5,6-TETRAHYDRO-2-(2-(3-R-O-PHENYL)ETHYL)PYRIMIDINES, 1,4,5,6 - TETRAHYDRO-2-(2-(O-R-O-PHENYL)VINYL) PYRIMIDINES AND THE CORRESPONDING 2-IMIDAZOLINES; AND N-METHYL - N - SUBSTITUTED 3-(3-R-O-PHENYL)PROPIONAMIDINES AND THE CORRESPONDING ACRYLAMIDINES WHEREIN R-O, IS HYDROXY OR A GROUP CONVERTIBLE TO HYDROXY, IS DESCRIBED.