Active ingredient combinations with insecticidal and acaricidal properties
Patent 7084138 Issued on August 1, 2006. Estimated Expiration Date: 
August 23, 2021. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.
August 23, 2021. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.Patent References 2758115 3264177 3309266 3748356 Substituted benzoyl ureas Certain substituted benzoyl urea insecticides Benzoyl phenyl urea derivatives having insecticidal activities Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides InventorsAssigneeApplicationNo. 10363153 filed on 08/23/2001US Classes:514/229.8, Tricyclo ring system having the six-membered hetero ring as one of the cyclos514/245, Nitrogen bonded directly to ring carbon of the hetero ring514/407, Chalcogen or nitrogen bonded directly to the pyrazole ring by nonionic bonding514/409, Spiro ring system514/423, C=X bonded directly to the five-membered hetero ring by nonionic bonding (X is chalcogen)514/425, Plural chalcogens bonded directly to the five-membered hetero ring by nonionic bonding514/383, 1,2,4-triazoles (including hydrogenated)514/594, Additional C=O bonded directly to urea nitrogen514/482, N-C(=X)-N, N-C(=N)N, N-N, nitrogen directly bonded to oxygen by nonionic bonding or cyano containing560/16, Nitrogen in acid moiety514/344, Cyano bonded directly to the six-membered hetero ring514/63, Silicon containing DOAI514/587, Oxygen containing564/442, Halogen, bonded directly to carbon, containing514/426, Nitrogen bonded directly to the five-membered hetero ring by nonionic bonding546/226, At 1-position560/358, Benzene ring bonded directly to the isocyanate group564/149, Substituent Q contains benzene ring514/224.2, Polycyclo ring system having the six-membered hetero ring as one of the cyclos (e.g., 1,3- and 1,4- benzothiazines, etc.)549/404, Nitrogen bonded directly to the bicyclo ring system548/533, Additional -C(=X) bonded directly to the five-membered hetero ring (e.g., N n-butyryl-L-proline, etc.)504/283, Hetero ring is five-membered consisting of one nitrogen and four carbons514/411, Tricyclo ring system having the five-membered hetero ring as one of the cyclos560/27, Plural rings in acid moiety548/543, Chalcogen bonded directly to a ring carbon of the five-membered hetero ring which is adjacent to the ring nitrogen (e.g., 2-pyrrolidones, etc.)548/557, Nitrogen attached directly to the five-membered hetero ring by nonionic bonding548/317.5, Three chalcogens bonded directly to ring carbons of the diazole ring514/456, Bicyclo ring system having the hetero ring as one of the cyclos (e.g., chromones, etc.)534/885, Benzene ring bonded directly to the azo group514/422, Additional hetero ring504/138, Hetero ring is five-membered including nitrogen514/374, 1,3-oxazoles (including hydrogenated)514/452, Plural ring oxygens in the hetero ring514/468, Polycyclo ring system having the hetero ring as one of the cyclos514/406, Pyrazoles514/91, Hetero ring is five-membered548/365.1, Plural 1,2-diazoles (including hydrogenated)504/225, Additional hetero ring containing544/165, Carbocyclic ring bonded directly to the nitrogen504/238, Chalcogen bonded directly to ring carbon of the diazine ring544/212, Hetero ring426/532, With biocide or biostat504/195, Hetero ring containing504/282, Chalcogen or nitrogen bonded directly to ring carbon of the diazole ring514/350, C=O bonded directly to the six-membered hetero ring504/284, Polycyclo ring system having the five-membered hetero ring as one of the cyclos (e.g., indoles, etc.)514/424, Chalcogen bonded directly to the five-membered hetero ring by nonionic bonding514/343, The additional hetero ring consists of one nitrogen and four carbons (e.g., nicotine, etc.)514/533, Compound contains two or more C(=O)O groups indirectly bonded together by only conalent bonds504/292, The hetero ring is six-membered549/265, The spiro includes the lactone ring514/462, Spiro ring system560/76, Polycarboxylic acid514/444, Additional hetero ring548/408, The spiro includes the five-membered hetero ring560/39, Oxy in acid moiety548/541, Chalcogen attached directly to the five-membered hetero ring by nonionic bonding (e.g., 3-pyrrolidinols, etc.)514/432The hetero ring is six-memberedExaminersPrimary: Clardy, S. MarkAttorney, Agent or FirmForeign Patent References
International ClassA01N 43/36AbstractThe invention relates to novel active compound combinations having very good insecticidal and acaricidal properties and containing (a) cyclic ketoenols having the formulain which the groups W, X, Y, Z, A, B, D, and G have the meanings given in the disclosure, and (b) the active compounds (1) to (22) listed in the disclosure. Other References
Field of SearchTricyclo ring system having the six-membered hetero ring as one of the cyclosNitrogen bonded directly to ring carbon of the hetero ring Chalcogen or nitrogen bonded directly to the pyrazole ring by nonionic bonding Spiro ring system C=X bonded directly to the five-membered hetero ring by nonionic bonding (X is chalcogen) Plural chalcogens bonded directly to the five-membered hetero ring by nonionic bonding The cyano is bonded directly to a benzene ring |
| ||||||||||||||
