Abstract: The present invention discloses an isoxazoline compounds of formula (I), wherein, R1, R2, R4, R5, R6, A, W and n are as defined in the detailed description. The present invention further discloses methods for preparation of compounds of formula (I) and use of the compounds of formula (I) as a pest control agent.

Abstract: The present invention discloses a process for the preparation of substituted pyridine compounds of formula (I), comprises a step in which vinylogous nitriles of formula (II), are obtained from substituted ?,?-unsaturated nitrile compounds of formula (III), and a further step of converting the vinylogous nitrile compounds of formula (II) into substituted pyridines of formula (I); wherein R1, R2, R3, R4 and LG are as defined in the description.

Abstract: The present invention discloses a novel agrochemical composition comprising (1) at least one compound of formula (I) wherein, R1, R2, R3, R4, R5, R6, R7 and n are as defined in the detailed description and (2) at least one further active ingredient. The present invention further discloses a method for controlling the phytopathogenic fungi of plants using the agrochemical composition according to invention.

Abstract: A container (10) having tamper evident features comprising: a bottle (12) having a neck (34) with an opening (14) at a distal end (16) and a base (20) at a proximal end (18) thereof; a cap (22) received on the neck (34) and movably retained on the bottle (12) wherein the cap (22) includes a first tamper evident feature (24) to provide an indication of tampering to an end user, the cap (22) further includes a second tamper evident feature (32) which becomes visible only when the first tamper evident feature (24) removed partially or completely from the bottle (12).

Abstract: The present invention disclosed a process for the synthesis of compound of formula (Z) or a salt thereof, wherein, R, R1, R2, R3 and R10 are as defined in the detailed description. The process further comprises the synthesis of an anthranilic diamide compound of formula (I).

Abstract: The present invention discloses a process for the synthesis of compound of formula (VII) or a salt thereof, wherein, R, R1, R2, R3, R4a and R4b are as defined in the detailed description. The process further comprises the synthesis of an anthranilic diamide compound of formula (I).

Abstract: The present invention relates to a pesticidal active mixture comprising thietanyloxy compound of formula (I), oxides or a salt thereof, wherein, R1, R2, R3, R4, R5, and R6 are as defined in the description, and at least one insecticidally active compound (II) or at least one fungicidally active compound (III).

Abstract: The present invention relates to a pesticidal active mixture comprising pyrazolopyridine anthranilamide compound of formula (I), oxides or a salt thereof, wherein, R1, R2, R3, R4, Z and E are as defined in the description, and at least one insecticidally active compound (II) or at least one fungicidally active compound (III).

Abstract: The present invention disclosed a process for the synthesis of anthranilic diamide compound of formula (I), wherein, R1, R2, R3a, R3b, R3c, R4, R5, R6 and Z are as defined in the detailed description. The process comprising the step of obtaining a mono- or dicyano substituted aniline compound of formula (IV) which is then converted to an anthranilic acid compound of formula (V) or an anthranilic amide compound of formula (Va).

Abstract: The present invention discloses a fused heterocyclic compound of formula (I), wherein, Q, R1, R2, n, m and Y are as defined in the detailed description. The present invention further discloses methods for their preparation and use of the compounds of formula (I) as a pest control agent.

Abstract: The present invention relates to a compound selected from formula (I) and a process for preparing the same wherein, R2, R3, A, Hy, K, n, m, X1, and W1 are as defined in the description. The invention also relates to the combination and composition comprising the compound of formula (I).

Abstract: The present invention relates to a compound formula (I) and a process for preparing the same, wherein, R2, A, E, Hy, Ra, n, Q and W1 are each as defined in the description. The invention also relates to the combination and composition comprising the compound of formula (I).

Abstract: The present invention relates to 4-substituted phenylamidine derivatives of the general formula (I), wherein R5-R6, ArA4, D, G, B, Q and an integer m have the meanings as defined in the description. The invention further relates to methods for their preparation and use of said compounds for controlling undesired phytopathogenic microorganisms, and agents for said purpose, comprising said phenylamine derivatives. This invention further relates to a method for controlling undesired phytopathogenic microorganisms by application of said 4-substituted phenylamidine derivatives of general formula (I) to such undesired microorganisms and/or to their habitat, according to the invention.

Abstract: The present invention relates to a compound of formula (I), wherein, R1, A, A5, A6, A7, A8, R12, n and Q are as defined in the detailed description and a process for preparing the compound of formula (I). The present invention also relates to a method for controlling or preventing phytopathogenic fungi.

Abstract: The present invention discloses a fused heterocyclic compound of formula (I), wherein, R1, Y, Q, A, G, m and E are as defined in the detailed description. The present invention further discloses methods for their preparation and use of the compounds of formula (I) as a pest control agent.

Abstract: The present invention disclosed a process for the synthesis of anthranilic diamide compound of formula (I), wherein, R1, R2, R3a, R3b, R3c, R4, R5, R6 and Z are as defined in the detailed description. The process comprising the step of obtaining a mono- or dicyano substituted aniline compound of formula (IV) which is then converted to an anthranilic acid compound of formula (V) or an anthranilic amide compound of formula (Va). Further, the compound of formula (VI) can be optionally synthesized from compound of formula (IV or V or Va).

Abstract: The present invention relates to novel oxadiazoles of Formula I. wherein, R1, L1, A, L2 and R10 are as defined in the detailed description.

Abstract: The present invention discloses a compound of formula (I), wherein, R1, L1, A, k, R8, R9 L2 and R5 are as defined in the detailed description. The present invention also discloses a process for preparing the compound of formula (I).

Abstract: The present invention discloses a compound of formula (I), wherein, R1, L1, A, L2, W1, R2f, R3f, Q, and R10 are as defined in the detailed description. The present invention also relates to a process for preparing the compound of formula (I).

Abstract: The present invention relates a novel process for preparing a compound of Formula I, wherein, R1, R2, R3a, R3b, R3c, R4, R5, R6, R7 and Z are as defined in the description. The process comprises a novel and inventive step of converting a dione of Formula II into an isatoic anhydride of Formula V in a single step. wherein, R2 is F, Cl, Br or I; R1, R3a, R3b, R3c, R4, R5, R6, R7 and Z are as defined in the description.