| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 341 | 一种杀虫剂喷雾器 | CN202322440257.6 | 2023-09-08 | CN220831579U | 2024-04-26 | 何永芳 |
| 本实用新型涉及林业治理技术领域，具体涉及一种杀虫剂喷雾器，包括喷雾器箱体，其内部连接有隔离板；在箱体底部安装有蓄电池及电机；喷雾器操作杆，其安装在喷雾器箱体的左侧。本实用新型克服了现有技术的不足，通过设置限流器，雾化喷头以及直流喷雾管，使工作人员可以通过调节限流器，来控制雾化喷头喷水的大小以及方式，从而达到批量喷洒和选择性喷洒的目的；通过设置隔离板，隔离板的钝角造型，使得所有药液在重力的作用下，流向隔离板的拐角处，不再留有残留造成浪费；通过设置蓄电池、第一电机、与搅拌扇叶，在工作过程中为半自动装置，搅拌扇叶的设计能够更好的混合液体让搅拌更加充分，出水量也维持稳定，工作人员更加省时省力。 | ||||||
| 342 | 一种农业增产种植用驱虫装置 | CN201921618073.1 | 2019-09-26 | CN210869557U | 2020-06-30 | 吉丽珠 |
| 本实用新型公开了一种农业增产种植用驱虫装置，包括：撑架、侧架、连接座、调节筒、调节栓、调节柱、栓孔、管托、加强架等部件；使用时，将所述输药管连接加有杀虫驱虫剂并有一定水压的出水装置，将两个支撑行走装置对向设置于待杀虫驱虫处理农田的两侧，再根据作物的高度，选择性的，再调节调节筒内的调节柱的高度并固定，再将所述输药管的封堵端，依次穿过两个支撑行走装置的管托内，并由两个固定夹嵌套固定，再打开水阀，输药管上的喷口开始为农田进行除虫喷雾处理，再安排两个人员分别推动两个支撑行走装置尽量同步行进，对农田进行大规模一次性的杀虫驱虫作业也操作完成；本实用新型的有益效果是：效率高、可大面积进行杀虫剂喷洒。 | ||||||
| 343 | 一种单波长金龟子专用杀虫灯 | CN201420270993.X | 2014-05-24 | CN204157509U | 2015-02-18 | 郝明先 |
| 本实用新型公开了一种单波长金龟子专用杀虫灯，其特征在于，包括防雨顶盖（2）、滑动轨道（4）、引诱光源、高压电网（11）、锥形收集底盘（9）、电源箱（7）和定时装置（10），所述的引诱光源由Ⅰ号LED灯（5）和Ⅱ号LED灯（6）构成，所述的高压电网（11）、引诱光源和定时装置（10）分别与电源箱（7）通过导线连接，高压电网（11）呈环形设置于引诱光源周边，所述的防雨顶盖（2）与高压电网（11）通过滑动轨道（4）连接，所述的锥形收集底盘（9）上设置药槽（8）。本实用新型的杀虫灯晚上能对金龟子类群进行选择性诱杀，白天可以通过药槽中的杀虫剂杀灭害虫，雨天防雨效果明显，能延长诱虫灯的使用年限。 | ||||||
| 344 | 结合nAChR的新类烟碱的油分散体 | CN201080002006.2 | 2010-03-04 | CN102387705B | 2015-03-25 | V·卡萨纳希尔内; M·西梅诺谢拉; B·西梅诺谢拉 |
| 选择性昆虫新类烟碱是一类杀虫剂活性成分，它们在化学结构上具有某些共同的特征并且与nAChR乙酰胆碱受体结合。此类化合物在油混悬剂或油分散体中的制剂具有挑战性，这是由于在油性介质中由它们的杂原子的静电相互作用导致的所述油分散体的不可逆絮凝或均质性降低及渗出。通过使用分散于油中的某些基于共聚阴离子脂肪酸的分散剂、脱水山梨糖醇衍生物、离子表面活性剂、其他非离子表面活性剂和无机多价阳离子盐，成功地将吡虫啉、噻虫嗪、噻虫啉、烯啶虫胺、啶虫脒、噻虫胺和呋虫胺及它们的具有与nAChR结合能力的衍生物配制入油混悬剂中。以此方式产生的制剂在生理化学参数方面呈现出优异的储藏稳定性，包括新类烟碱活性成分的稳定性、降低的渗出和完全的可再分散性。此外，由于在水中稀释-乳化时降低的且均一的低于2μm的粒度，它们表现出优异的生物学有效性。 | ||||||
| 345 | 结合nAChR的新类烟碱的油分散体 | CN201080002006.2 | 2010-03-04 | CN102387705A | 2012-03-21 | V·卡萨纳希尔内; M·西梅诺谢拉; B·西梅诺谢拉 |
| 选择性昆虫新类烟碱是一类杀虫剂活性成分，它们在化学结构上具有某些共同的特征并且与nAChR乙酰胆碱受体结合。此类化合物在油混悬剂或油分散体中的制剂具有挑战性，这是由于在油性介质中由它们的杂原子的静电相互作用导致的所述油分散体的不可逆絮凝或均质性降低及渗出。通过使用分散于油中的某些基于共聚阴离子脂肪酸的分散剂、脱水山梨糖醇衍生物、离子表面活性剂、其他非离子表面活性剂和无机多价阳离子盐，成功地将吡虫啉、噻虫嗪、噻虫啉、烯啶虫胺、啶虫脒、噻虫胺和呋虫胺及它们的具有与nAChR结合能力的衍生物配制入油混悬剂中。以此方式产生的制剂在生理化学参数方面呈现出优异的储藏稳定性，包括新类烟碱活性成分的稳定性、降低的渗出和完全的可再分散性。此外，由于在水中稀释-乳化时降低的且均一的低于2μm的粒度，它们表现出优异的生物学有效性。 | ||||||
| 346 | 선택된 곤충을 유인살충하는 방법 및 그 장치 | KR1019810005141 | 1981-12-26 | KR1019870001843B1 | 1987-10-17 | 자네트케이하워스; 로버트트로이스타텐 |
| A selective insect control device is presented. The device for attracting specific insects to a predetermined site comprises (a) synthetic resin body contg. a pheromone(I) which is an attractant for the male or female insects, and (b) means for controlled release of (I) vapour form at a rate sufficient to attract the insects. The device minimises the amt. of insecticide per unit surface area and the amt. of insecticide required to obtain the maximum effect on the insect population at the predetermined site. | ||||||
| 347 | METHOD AND COMPOSITION FOR KILLING MALARIA PARASITES | PCT/US1992007380 | 1992-08-28 | WO1993004696A1 | 1993-03-18 | THOMAS JEFFERSON UNIVERSITY; TARASCHI, Theodore, F.; POUVELLE, Bruno |
| A composition and method for killing malaria parasites by selective delivery of parasiticidal agents, including antibodies and antibody-toxin conjugates are provided. | ||||||
| 348 | S-Difluoromethylhomocysteines, preparation process, and insecticidal compositions | EP89119424.3 | 1989-10-19 | EP0367033A1 | 1990-05-09 | Tsushima, Tadahiko; Ishihara, Shoichi |
Described are compounds of the general formula:
|
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| 349 | 말단 알킨과 아릴 토실레이트와의 팔라듐 촉매되는 커플링 방법 | KR1020097027504 | 2008-06-19 | KR1020100027181A | 2010-03-10 | 알키에크오마르; 나자레마르크; 린덴슈미트안드레아스; 우르만마티아스; 할란니스; 알룬소호르헤 |
| The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein R1; R2; R3; R4; R5; J and W have the meanings indicated in the claims. The present invention provides an efficient and general palladium-catalyzed coupling process for aryl tosylates with terminal alkynes to a wide variety of substituted, multifunctional aryl-1-alkynes of the formula (I) useful for the production of intermediates in the preparation for pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides. | ||||||
| 350 | 말단 알킨과 헤테로아릴 토실레이트 및 헤테로아릴 벤젠설포네이트의 팔라듐-촉매되는 커플링 방법 | KR1020097027541 | 2008-06-19 | KR1020100028068A | 2010-03-11 | 르키엑오마르; 나차레마르크; 린덴슈미트안드레아스; 알론소호르헤; 우르만마티아스; 할란니스 |
| The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), (I) wherein D, J and W have the meanings indicated in the claims. The present invention provides an efficient and general palladium-catalyzed coupling process of heteroaryl tosylates with terminal alkynes to a wide variety of substituted, multifunctional heteroaryl-1-alkynes of the formula I useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides. | ||||||
| 351 | 어닐링된 벤즈이미다졸 및 아자벤즈이미다졸의 위치선택적 금속 촉매된 합성 | KR1020097026783 | 2008-06-11 | KR1020100033484A | 2010-03-30 | 알론소호르헤; 린덴슈미트안드레아스; 나차레마르크; 알키엔오마르; 우르만마티아스; 할란니스 |
| A regioselective metal catalyzed synthesis of benzimidazoles and azabenzimidazoles The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein R1; R2; R3; R4; J1; J2; J3; J4 and G have the meanings indicated in the claims. The present invention provides a direct metal, e.g. palladium or copper, catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula (I) starting from 2-halo-nitroarenes and N-substituted amides useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides. | ||||||
| 352 | Composition for prevention and extermination of injurious insects and its preparation | JP5566677 | 1977-05-13 | JPS5324027A | 1978-03-06 | FUJIMOTO SATOAKI; OONO NOBUO; OKUNO KICHITOSHI; MIZUTANI TOSHIO; OONO ISAO; HIRANO MASACHIKA; ITAYA NOBUSHIGE; MATSUO HISASHI |
| PURPOSE: Low toxic insecticide containing alkenoic acid ester, having selective or non-selective insecticidal effect against coleopteron, lepidopteron, dipteron, orthoorthopteron, hemipteron, and mites, and even effective against resistant insects. COPYRIGHT: (C)1978,JPO&Japio | ||||||
| 353 | Composition for prevention and extermination of injurious insects and its preparation | JP5566577 | 1977-05-13 | JPS5324026A | 1978-03-06 | FUJIMOTO SATOAKI; OONO NOBUO; OKUNO KICHITOSHI; MIZUTANI TOSHIO; OONO ISAO; HIRANO MASACHIKA; ITAYA NOBUSHIGE; MATSUO HISASHI |
| PURPOSE: Low toxic insecticide containing cycloalkene alkanoic acid ester, having selective or non-selective insecticidal effect against coleopteron, lepidopteron, dipteron, orthopteron, hemipteron, and mites, and even effective against resistant insects. COPYRIGHT: (C)1978,JPO&Japio | ||||||
| 354 | 벤즈이미다졸 및 아자벤즈이미다졸의 위치선택적 구리 촉매화 합성 | KR1020097027120 | 2008-06-11 | KR1020100023907A | 2010-03-04 | 알론소호르헤; 린덴슈미트안드레아스; 나차레마르크; 우르만마티아스; 할란니스; 르키엑오마르 |
| The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4; Q and J have the meanings indicated in the claims. The present invention provides a direct copper catalyzed regioselective process to a wide variety of unsymmetrical, multifunctional/-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and/-substituted amides. The process is useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides. | ||||||
| 355 | 벤즈이미다졸 및 아자벤즈이미다졸의 위치선택적 팔라듐 촉매된 합성 | KR1020097000869 | 2007-06-30 | KR1020090029267A | 2009-03-20 | 아론소호르게; 린덴슈밋트안드레아스; 나자레마르크; 할란니스; 르크요크오마르; 우르만맛티아스 |
| The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein RO; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct palladium catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula (I) starting from 2-halo-nitroarenes and #/-substituted amides useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricitdes and arthropodicides. | ||||||
| 356 | COMPOSITIONS AND METHODS FOR CONTROLLING INSECTS | PCT/EP1999/009277 | 1999-11-15 | WO00028824A1 | 2000-05-25 | |
| Compositions and methods for controlling the population of insects are disclosed. The compositions include a feeding stimulant for a particular insect, an effective amount of a 1-arylpyrazole or nicotinyl insecticide to kill a desired insect, at a concentration which is not typically toxic when applied to a plant in the absence of a feeding stimulant and the insect consumes an ordinary amount of toxin during the course of normal feeding, but is toxic when applied in conjunction with a feeding stimulant which causes the insect to consume more of the toxin than would normally be consumed during normal feeding. The use of normally non-toxic amounts of insecticides allows one to minimize the residual insecticide present on the crops. Also, by using a selective feeding stimulant along with a normally non-lethal concentration of insecticide, beneficial insects which are not attracted to the feeding stimulant are not effectively killed off, and detrimental insects which are attracted to the feeding stimulant are effectively killed off. | ||||||
| 357 | P,P'-Disubstituted .alpha.-trichloromethylbenzylphenyl ethers | US528351 | 1974-11-29 | US3966824A | 1976-06-29 | Robert L. Metcalf; Inder Kapoor; Asha Hirwe |
| P,P'-DISUBSTITUTED .alpha.-TRICHLOROMETHYLBENZYLPHENYL ETHERS ARE A NEW CLASS OF COMPOUNDS WHICH SHOW VARYING DEGREES OF UTILITY AS SELECTIVE OR NONSELECTIVE BIODEGRADABLE INSECTICIDES AND/OR LARVICIDES. | ||||||
| 358 | P,P'-Disubstituted .alpha.-trichloromethylbenzylanilines | US318085 | 1972-12-26 | US3941842A | 1976-03-02 | Robert L. Metcalf; Inder Kapoor; Asha Hirwe |
| P,P'-DISUBSTITUTED .alpha.-TRICHLOROMETHYLBENZYLANILINES ARE A NEW CLASS OF COMPOUNDS WHICH SHOW VARYING DEGREES OF UTILITY AS SELECTIVE OR NONSELECTIVE BIODEGRADABLE INSECTICIDES AND/OR LARVICIDES. | ||||||
| 359 | P,P{40 -Disubstituted alpha-trichloromethylbenzyl ethers | US31820672 | 1972-12-26 | US3894092A | 1975-07-08 | METCALF ROBERT L; KAPOOR INDER; HIRWE ASHA |
| P,P''-Disubstituted Alpha -trichloromethylbenzylphenyl ethers are a new class of compounds which show varying degrees of utility as selective or nonselective biodegradable insecticides and/or larvicides.
|
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| 360 | Ｎ-아미노인돌의 전이 금속 촉매된 합성 | KR1020097021379 | 2008-03-29 | KR1020100015546A | 2010-02-12 | 할란니스; 나자레엠; 린덴슈밋트안드레아스; 르크예크오마르; 우르만맛티아스; 알론소호르헤 |
| The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein R0; R1; R2; R3; R4; R5; R6; A1; A2; A3; A4, Q, T and J have the meanings indicated in the claims. The present invention provides a direct transition metal catalyzed process to a wide variety of multifunctional N-aminoindole or N-amino-azaindoles of the formula (I) from 2-halo-phenylacetylenes or (2-sulfonato)phenyl-acetylenes and N,N-disubstituted hydrazines, useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides. | ||||||
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