选择性杀虫剂相关的专利数据

序号	专利名	申请号	申请日	公开（公告）号	公开（公告）日	发明人
61	S-difluoromethylhomocysteines, preparation process, and selective insecticides containing them	US706266	1991-05-28	US5166425A	1992-11-24	Tadahiko Tsushima; Shoichi Ishihara
A compound of the formula: ##STR1## wherein R and R' each is hydrogen or a protecting group, or acid addition salts thereof, useful as a selective insecticide.
62	ANTIMICROBIAL PERACID COMPOSITIONS WITH SELECTED CATALASE ENZYMES AND METHODS OF USE IN ASEPTIC PACKAGING	PCT/IB2009/051610	2009-04-17	WO2009128049A2	2009-10-22	HERDT, Brandon L.; MAGNUSON, Joshua P.; MCSHERRY, David D.; LI, Junzhong; OWENS, Krista L.
The present invention relates to specially selected catalase enzymes and their use in reducing hydrogen peroxide in applications, and particularly in aseptic packaging applications.
63	ANTIMICROBIAL PERACID COMPOSITIONS WITH SELECTED CATALASE ENZYMES AND METHODS OF USE IN ASEPTIC PACKAGING	PCT/IB2009051253	2009-03-25	WO2009127986A2	2009-10-22	HERDT BRANDON L; MAGNUSON JOSHUA PM; MCSHERRY DAVID D; LI ZUNZHONG; OWENS KRISTA L
The present invention relates to specially selected catalase enzymes and their use in reducing hydrogen peroxide in applications, and particularly in aseptic packaging applications.
64	Selective Insecticides and/or Acaricides Based on Substituted Cyclic Dicarbonyl Compounds and Safeners	US11632501	2005-07-18	US20080200499A1	2008-08-21	Reiner Fischer; Udo Reckmann; Chris Rosinger; Erich Sanwald; Christian Arnold
The present invention relates to the use of selective insecticidal and/or acaricidal compositions, characterized in that they comprise an effective amount of an active compound combination comprising (a) at least one substituted cyclic dicarbonyl compound of the formula (I) in which W, X, Y and Z are as defined in the description and CDC is one of the dicarbonyl radicals mentioned in the description, and (b) at least one crop plant compatibility-improving compound from the group of compounds given in the description. for controlling insects and/or arachnids, and also to a method for controlling insects and/or arachnids using the compositions.
65	以取代的環酮烯醇類及安全劑為底之選擇性殺蟲劑 SELECTIVE INSECTICIDES BASED ON SUBSTITUTED CYCLIC KETOENOLS AND SAFENERS	TW094124480	2005-07-20	TW200616543A	2006-06-01	佛倫恩 FISCHER, REINER; 若又得 RECKMANN, UDO; 羅克根 ROSINGER, CHRISTOPHER HUGH; 孫愛其 SANWALD, ERICH; 羅克亭 ARNOLD, CHRISTIAN
本發明係有關選擇性殺蟲組合物於控制昆蟲與／或蜱上之用途，其特徵在於其包含有效量之活性化合物組合，其包含(a)至少一種式(I)化合物094124480-p01.bmp其中CKE、W、X、Y與Z如說明書中之定義，及(b)至少一種改善作物相容性之化合物，其係選自本說明書所述及之群中，及使用該組合物控制昆蟲與／或蜱之方法。
66	以取代的環酮烯醇類及安全劑為底之選擇性殺蟲劑 SELECTIVE INSECTICIDES BASED ON SUBSTITUTED CYCLIC KETOENOLS AND SAFENERS	TW094124480	2005-07-20	TWI368481B	2012-07-21	佛倫恩; 若又得; 羅克根; 孫愛其; 羅克亭
本發明係有關選擇性殺蟲組合物於控制昆蟲與/或蜱蟎上之用途，其特徵在於其包含有效量之活性化合物組合，其包含(a)至少一種式(I)化合物其中CKE、W、X、Y與Z如說明書中之定義，及(b)至少一種改善作物相容性之化合物，其係選自本說明書所述及之群中，及使用該組合物控制昆蟲與/或蜱蟎之方法。
67	Insecticidal N-(optionally substituted) - N'-substituted-N,N'-disubstituted- hydrazines	EP87303296.5	1987-04-15	EP0286746B1	1991-02-27	Hsu, Adam Chi-Tung; Hamp, Donald Wesley

68	할로알킬니코틴산 유도체, 안트라닐산 디아미드 또는프탈산 디아미드 및 약해 완화제를 기본으로 하는 선택적살충제	KR1020077003797	2005-07-18	KR1020070039146A	2007-04-11	피셔라이너; 피셔뤼디거; 푼케크리스티안; 헨제아힘; 안더쉬볼프람; 훈겐베르크하이케; 틸레르트볼프강; 렉크만우도; 빌름스로타르; 아르놀트크리스티안
본 발명은 성분으로서, (a) (1) 적어도 하나의 하기 일반식 (I)의 할로알킬니코틴산 유도체 또는 (2) 적어도 하나의 하기 일반식 (II)의 프탈산 디아미드 또는 (3) 적어도 하나의 하기 일반식 (III)의 안트라닐아미드, 및 (b) 명세서에 주어진 화합물 그룹, 특히 클로퀸토세트-멕실, 이속사디펜-에틸 및 메펜피르-디에틸중에서 선택된 적어도 하나의 작물 화합성 개선 화합물을 포함한 유효량의 활성 배합물을 포함함을 특징으로 하는 선택적 살충 조성물의 곤충 및/또는 거미류를 구제하기 위한 용도 및 이들 조성물을 사용하여 곤충 및/또는 거미류를 구제하는 방법에 관한 것이다: 상기 식에서, A ^A , R ^1A , X ^B , R ^1B , R ^2B , R ^3B , L ^1B , L ^2B , L ^3B , A ^1C , A ^2C , X ^C , R ^1C , R ^2C , R ^3C , R ^4C , R ^5C , R ^7C , R ^8C 및 R ^9C 는 명세서에 정의된 바와 같다.
69	Compounds with antidotal activity for the defence of cultivations of agrarian interest from the action of non-selective weed-killers	EP84108943.6	1984-07-27	EP0133970B1	1989-05-31	Palla, Ottorino, Dr.; Camaggi, Giovanni; Gozzo, Franco, Dr.; Signorini, Ernesto

70	Selective insecticides based on haloalkylnicotinic acid derivatives, anthranilic acid diamides, or phthalic acid diamides and safeners	US11572362	2005-07-18	US08017632B2	2011-09-13	Reiner Fischer; Rüdiger Fischer; Christian Funke; Achim Hense; Wolfram Andersch; Heike Hungenberg; Wolfgang Thielert; Udo Reckmann; Lothar Willms; Christian Arnold
The present invention relates to the use of selective insecticidal compositions, characterized by an effective amount of an active compound combination comprising (a) (1) at least one haloalkylnicotinic acid derivative of the formula (I) in which AA and R1A are as defined in the description, or (2) at least one phthalic acid diamide of the formula (II) in which XB, R1B, R2B, R3B, L1B, L2B and L3B are as defined in the description, or (3) at least one anthranilamide of the formula (III) in which A1C, A2C, XC, R1C, R2C, R3C, R4C, R5C, R7C, R8C and R9C are as defined in the description, and (b) at least one crop plant compatibility-improving compound from the group of compounds given in the description, in particular cloquintocet-mexyl, isoxadifen-ethyl and mefenpyr-diethyl for controlling insects and/or arachnids, and a method for controlling insects and/or arachnids using the compositions.
71	Selective Insecticides Based on Haloalkylnicotinic Acid Derivatives, Anthranilic Acid Diamides, or Phthalic Acid Diamides and Safeners	US11572362	2005-07-18	US20080221167A1	2008-09-11	Reiner Fischer; Rudiger Fischer; Christian Funke; Achim Hense; Wolfram Andersch; Heike Hungenberg; Wolfgang Thielert; Udo Reckmann; Lothar Willms; Christian Arnold
The present invention relates to the use of selective insecticidal compositions, characterized by an effective amount of an active compound combination comprising(a) (1) at least one haloalkylnicotinic acid derivative of the formula (I) in which AA and R1A are as defined in the description, or (2) at least one phthalic acid diamide of the formula (II) in which XB, R1B, R2B, R3B, L1B, L2B and L3B are as defined in the description, or (3) at least one anthranilamide of the formula (III) in which A1C, A2C, XC, R1C, R2C, R3C, R4C, R5C, R7C, R8C and R9C are as defined in the description, and (b) at least one crop plant compatibility-improving compound from the group of compounds given in the description, in particular cloquintocet-mexyl, isoxadifen-ethyl and mefenpyr-diethyl for controlling insects and/or arachnids, and a method for controlling insects and/or arachnids using the compositions.
72	제초활성을 갖는2-(5-옥시란일메톡시페닐)-4,5,6,7-테트라히드로-2Ｈ-인다졸유도체	KR1020030021052	2003-04-03	KR1020040086696A	2004-10-12	전동주; 김형래; 송종환; 장규환; 황인택
PURPOSE: Herbicidal2-(5-oxiranylmethoxyphenyl)-4,5,6,7-tetrahydro-2H-indazole derivatives are provided, which compounds have improved herbicidal effects and selectivity, so that the compounds can selectively kill weeds. CONSTITUTION: The herbicidal2-(5-oxiranylmethoxyphenyl)- 4,5,6,7-tetrahydro-2H-indazole derivatives represented by formula (1) are provided, wherein R1, R2 and R3 are independently hydrogen, C1-C5 alkyl, phenyl or substituted phenyl with 1 to 3 of halogen atoms. The method for preparing the herbicidal2-(5-oxiranylmethoxyphenyl)- 4,5,6,7-tetrahydro-2H-indazole derivatives of formula (1) comprises the steps of: reacting a compound of formula (2) with allyl halide in the presence of base to prepare a compound of formula (3); and introducing epoxy group into a double bond of the compound of formula (3), wherein X is halogen.
73	Controlling leafminer insects with selected carbamate insecticides,including 3,5-dimethyl-4-dimethylamino-methyl phenyl-n-methylcarbamate	US3507962D	1969-05-09	US3507962A	1970-04-21	TAYLOR JAMES L

74	PROCESS FOR THE SELECTIVE UTILIZATION OF THE HERBICIDE IMAZETAPIR IN POST-EMERGENCE AND CULTIVATING VARIETIES OF SUNFLOWERS WHICH ARE RESISTANT OR TOLERANT TO SAID HERBICIDE AND APPLICATION TO THE CONTROL OF THE PARASITE FOXTAIL WEEDS OROBANCHE CERNUA LOEFL./O. CUMANA WALLER	PCT/ES1999/000053	1999-03-03	WO99065312A1	1999-12-23
The process comprises a solution of imazetapir in the post-emergence phase of said sunflower culture simply or repeatedly by means of a conventional applicator while regulating the pressure and the volume of the solution to be applied per surface unit. The process can be applied essentially to the control of the parasite weeds foxtail in emerged sunflower cultures.
75	Process for the stereoselective preparation of insecticide 6,7,8,9,10-10-hexahalo-1, 5, 5a, 6, 9, 9a-hexadro-6, 9-methano-2, 4, 3-benzodioxathiepin-3-oxide	US10474029	2003-10-10	US20040092751A1	2004-05-13	Ashwin Champraj Shroff; Abhijit Premvallabh Purohit; Sanjay Dhirajlal Vadoraria
A process for the stereoselective preparation of insecticide 6,7,8,9,10,10-hexahalo-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide of the general formula 1: 1 wherein X is a halogen such as fluorine, chlorine or bromine. The process comprises reacting 1,4,5,6,7,7-hexahalo-5-norbornene-2,3-dimethanol of the general formula IV: 2 wherein X is as defined above, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139null C., wherein the reaction is carried out in the presence of a stereo isomer directing agent comprising an isomer of the compound of the formula I different from the desired isomer. The molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula IV is a least 0.07.
76	Process for the stereoselective preparation of insecticide 6,7,8,9,10-10-hexahalo-1,5,5a,6,9,9a-hexadro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide	US10474029	2003-10-10	US06831179B2	2004-12-14	Ashwin Champraj Shroff; Abhijit Premvallabh Purohit; Sanjay Dhirajlal Vadodaria
A process for the stereoselective preparation of insecticide 6,7,8,9,10,10-hexahalo-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide of the general formula I: wherein X is a halogen such as fluorine, chlorine or bromine. The process comprises reacting 1,4,5,6,7,7-hexahalo-5-norbornene-2,3-dimethanol of the general formula IV: wherein X is as defined above, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139° C., wherein the reaction is carried out in the presence of a stereo isomer directing agent comprising an isomer of the compound of the formula I different from the desired isomer. The molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula IV is at least 0.07.
77	A PROCESS FOR THE STEREOSELECTIVE PREPARATION OF INSECTICIDE 6,7,8,9,10-10-HEXAHALO-1,5,5A,6,9,9A-HEXAHYDRO-6,9-METHANO-2,4,3-BENZODIOXATHIEPIN-3-OXIDE	PCT/IN0100092	2001-04-24	WO02085884A8	2003-01-30	SHROFF ASHWIN CHAMPRAJ; PUROHIT ABHIJIT PREMVALLABH; VADORARIA SANJAY DHIRAJLAL
A process for the stereoselective preparation of insecticide 6,7,8,9,10,10-hexahalo-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide of general formula (I), wherein X is a halogen such as fluorine, chlorine or bromine. The process comprises reacting 1,4,5,6,7,7-hexahalo-5-norbornene-2,3-dimethanol of the general formula IV: wherein X is as defined above, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139 DEG C, wherein the reaction is carried out in the presence of a stereo isomer directing agent comprising an isomer of the compound of the formula (I) different from the desired isomer. The molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula (IV) is at least 0.07.
78	A PROCESS FOR THE STEREOSELECTIVE PREPARATION OF INSECTICIDE 6,7,8,9,10-10-HEXAHALO-1,5,5A,6,9,9A-HEXAHYDRO-6,9-METHANO-2,4,3-BENZODIOXATHIEPIN-3-OXIDE	PCT/IN2001/000092	2001-04-24	WO2002085884A1	2002-10-31	SHROFF, Ashwin, Champraj; PUROHIT, Abhijit, Premvallabh; VADORARIA, Sanjay, Dhirajlal
A process for the stereoselective preparation of insecticide 6,7,8,9,10,10-hexahalo-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxie of the general formula 1: wherein X is a halogen such as fluorine, chlorine or bromine. The process comprises reacting 1,4,5,6,7,7-hexahalo-5-norbornene-2,3-dimethanol of the general formula IV: wherein X is as defined above, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139 °C, wherein the reaction is carried out in the presence of a stereo isomer directing agent comprising an isomer of the compound of the formula I different from the desired isomer. The molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula IV is at least 0.07.
79	인간 피부 표피의 기저 케라티노사이트의 비율을 제어하고 서바이빈의 핵 형태를 발현하는 활성제로서 Ｎ-팔미토일 알라닌, Ｎ-팔미토일 글리신, Ｎ-팔미토일 이소류신 및 Ｎ-코코일 알라닌 중에서 선택된 Ｎ-아실 아미노산의 용도, 및 이를 포함하는 노화 방지 화장품 조성물	KR1020117004925	2009-07-24	KR101652541B1	2016-08-30	드몽산디; 카투자토래티시아; 스똘쯔꼬린느; 세브로나탈리
본발명은인간피부표피의기저케라티노사이트의비율을제어하고서바이빈의핵 형태를발현하는활성제로서 N-팔미토일알라닌, N-팔미토일글리신, N-팔미토일이소류신및 N-코코일알라닌중에서선택된 N-아실아미노산의용도, 이를포함하는노화방지화장품조성물, 및이의인간피부표피에서줄기세포의생존을유지하기위한치료방법의수행에있어서의용도에관한것이다.
80	一种金佛手精油在制备线虫杀虫剂中的应用	CN201811524374.8	2018-12-13	CN109497104A	2019-03-22	易封萍; 朴栖西
本发明提供了一种金佛手精油在制备线虫杀虫剂中的应用。本发明的植物源杀虫剂金佛手精油具有良好的杀虫活性，尤其是对秀丽隐杆线虫这种多细胞生物为新型植物源杀虫剂防治线虫提供了新的选择性。

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