CAS: 153719-23-4; Thiamethoxam

该化合物是一种新尼可类杀虫剂,对各种害虫,包括吸食昆虫和白灌木提供长期的系统控制. 它的独特性使它能被植物吸收,保护人们免受植根害虫的侵扰,同时控制叶害虫,最大限度地减少对多种用途的需要.

结构式图片

欧盟法规

统一分类与标签REACH注册ECHA物质欧盟农药活性物质食品接触材料-禁用CMR物质OtherC&L通报欧盟生物杀灭剂法规欧盟《生物杀灭剂法规》REACH预注册废弃物危险特性清单"欧盟管控危险化学品"工作场所安全标识要求ECHA物质化妆品禁用物质清单

上下游产品

CAS号105827-91-6 2-氯-5-氯甲基噻唑 | CAS号153719-38-1 3-甲基-4-硝基亚胺四氢-1... | CAS号135018-15-4 2-[(2-chloro-1,...

合成工艺路线路线简述

  • 合成目标产物 Thiamethoxam 主要起始原料 2-Chloro-5-Chloromethylthiazole And 3,6-Dihydro-3-Methyl-N-Nitro-2H-1,3,5-Oxadiazin-4-Amine
  • (文献来源)合成步骤主要原料 2-Chloro-5-Chloromethylthiazole 和 3,6-Dihydro-3-Methyl-N-Nitro-2H-1,3,5-Oxadiazin-4-Amine
噻虫嗪杂质3置于盐酸,氯体系中,用 水,氯苯 用作溶剂,化学反应 6.0H,反应生成噻虫嗪
参考文献:Process For The Preparation Of Thiazole Derivatives
标题:Process For The Preparation Of Thiazole Derivatives
摘要:本发明涉及一种制备式中q,Y,Z,R1,R2,R3,R4和r5如规范中所定义的化合物的方法,包括:A)将式(I)的化合物与卤化剂反应形成式(II)的化合物;B)通过卤化剂将式(II)的化合物转化为式(III)的化合物;可选c)将式(Iv)的化合物转化为式(III)的化合物;D)通过式的化合物将式(III)的化合物转化为式(V)的化合物;E)通过式(V)的化合物将式(Iv)的化合物转化为式(Vi)的化合物;F)通过氯化剂将式(Vi)的化合物转化为式(I)的化合物;以及制备化合物(III)和制备化合物(Iv)的方法.

海关参考信息

专利信息


专利号:WO-2025056767-A1
优先权日:2023-09-15
标题 :Process for the preparation of enantiomerically enriched aliphatic amines
发明人:BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS
权利人:SYNGENTA CROP PROTECTION AG
摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.

专利号:US-2016073631-A1
优先权日:2013-03-04
标 题 :Process for the preparation of dihydropyrrole derivatives
发明人:EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS
权利人:SYNGENTA PARTICIPATIONS AG; SYNGENTA LTD
摘要:The present invention provides stereoselective processes for the preparation of compounds of formula (I) n n n n n n n n n n n n wherein n P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; n R 1 is chlorodifluoromethyl or trifluoromethyl; n R 2 is optionally substituted aryl or optionally substituted heteroaryl; n n is 0 or 1; n including the process comprising n (a-i) reacting a compound of formula II n n n n n n n n n n n n n n n n wherein P, R 1 and R 2 are as defined for the compound of formula I; n with nitromethane in the presence a chiral catalyst to give a compound of formula III n n n n n n n n n n n n n n n n wherein P, R 1 and R 2 are as defined for the compound of formula I; and n (a-ii) reductively cyclising the compound of formula III to give the compound of formula I. n n n n n The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).

专利号:US-9233920-B2
优先权日:2010-06-11
标题 :Process for the preparation of dihydropyrrole derivatives
发明人:EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS
权利人:EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS; SYNGENTA PARTICIPATIONS AG; SYNGENTA LTD
摘要:The present invention provides stereoselective processes for the preparation of compounds of formula (I) wherein P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; R 1 is chlorodifluoromethyl or trifluoromethyl; R 2 is optionally substituted aryl or optionally substituted heteroaryl; n is 0 or 1; including the process comprising (a-i) reacting a compound of formula II wherein P, R 1 and R 2 are as defined for the compound of formula I; with nitromethane in the presence a chiral catalyst to give a compound of formula III Wherein P, R 1 and R 2 are as defined for the compound of formula I; and (a-ii) reductively cyclizing the compound of formula III to give the compound of formula I. The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).

专利号:US-11751567-B2
优先权日:2021-09-23
标 题:Steroidal piperidone derivative, synthesis method, and use thereof
发明人:SHI BAOJUN; JIANG WEIQI; MA SHICHUANG; HU YUXIAO; WANG QIANGPING
权利人:UNIV NORTHWEST A&F
摘要:A steroidal piperidone derivative, a synthesis method, and a use thereof are provided. The steroidal piperidone derivative has a chemical structure shown in general formula (1) or general formula (2), where R is any one selected from the group consisting of alkyl, phenyl, substituted phenyl, and a heterocycle. In the synthesis method of the steroidal piperidone derivative, dehydroepiandrosterone (DHEA) is used as a basic raw material to prepare the steroidal piperidone derivative of the present disclosure through a series of reactions. A product prepared by the synthesis method has a high yield and is easily separated, and thus the synthesis method is the optimal method for preparing the steroidal piperidone derivative of the present disclosure. The present steroidal piperidone derivative exhibits prominent toxic activity against sucking pests, such as aphids, spider mites, rice planthoppers, and B. tabaci, and can be used for the control of a plant pest.

专利号:US-10906880-B2
优先权日:2016-01-26
标题:Kind of isothiazole oxime ether-containing strobilurin derivatives and its preparation methods and application
发明人:FAN ZHIJIN; CHEN LAI; GUO XIAOFENG; ZHU YUJIE; QIAN XIAOLIN; MA LIUYONG; ZHANG NAILOU; WANG HAIXIA; ZHANG ZHIMING; XU JINGHUA; SONG YINQI
权利人:UNIV NANKAI
摘要:The present invention is that provided a synthesis method of a series of isothiazole oxime ether containing strobilurin derivatives IV. The present invention relates to 3,4-dichloroisothiazolyl oxime ether strobilurin derivatives, and their chemical structural formula is as shown by IV. n n n n n n n n n n The invention discloses the structural formula of the above compound, the synthesis method and the use as an insecticide, a fungicide, an anti-plant virus agent, and an agriculturally acceptable auxiliary or synergist and a commercial insecticide. The use of a fungicide, an anti-plant virus agent and an acaricide in combination for controlling agricultural, forestry, horticultural plant pests, diseases, virus diseases and preparation methods.

专利号:US-9468207-B2
优先权日:2012-04-12
标 题 :Insecticide and acaricide paints that inhibit chitin synthesis, regulate insect juvenile hormone and repel arthropods, for controlling endemic diseases, pests and allergens
发明人:MATEO HERRERO MARIA PILAR
权利人:MATEO HERRERO MARIA PILAR
摘要:The present invention relates to insecticide and acaricide paints that inhibit chitin synthesis, regulate insect juvenile hormone and repel arthropods, for controlling endemic diseases, pests and allergens. The paints comprise at least the following compounds (in any combination): 1%-100% water, 0.0001%-20% insecticides, 0.0001%-20% chitin inhibitor, 0.0001%-20% juvenile hormone regulator, 1%-50% polymers, 0%-40% pigments, 0%-60% fillers, 0%-60% natural repellents, and 0.01%-20% stabilizers. The composition of the paints allows the active ingredients to be encapsulated in an aqueous polymer with or without the incorporation of fillers and pigments, and therefore the range of use thereof is increased.
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主要参考文献


1: Zhang Q, Wang X, Li Z, Jin H, Lu Z, Yu C, Huang YF, Zhao M. Simultaneous determination of nine neonicotinoids in human urine using isotope-dilution ultra-performance liquid chromatography-tandem mass spectrometry. Environ Pollut. 2018 May 14;240:647-652. doi: 10.1016/j.envpol.2018.04.144. [Epub ahead of print] pii: E1165. doi: 10.3390/molecules23051165. doi: 10.1007/s00436-018-5891-x. Epub 2018 Apr 30. doi: 10.1016/j.scitotenv.2018.04.128. [Epub ahead of print] doi: 10.1016/j.scitotenv.2018.04.292. [Epub ahead of print] doi: 10.1007/s10661-018-6655-x. doi: 10.3389/fphys.2018.00322. eCollection 2018.
12: Moyakao K, Santaladchaiyakit Y, Srijaranai S, Vichapong J. Preconcentration of Trace Neonicotinoid Insecticide Residues Using Vortex-Assisted Dispersive Micro Solid-Phase Extraction with Montmorillonite as an Efficient Sorbent. Molecules. 2018 Apr 11;23(4). pii: E883. doi: 10.3390/molecules23040883. doi: 10.1016/j.etap.2018.04.002. [Epub ahead of print] doi: 10.1016/j.chemosphere.2018.03.115. Epub 2018 Mar 19. doi: 10.1177/0748233718762609. Epub 2018 Mar 28. doi: 10.1016/j.chemosphere.2018.02.108. Epub 2018 Mar 21. e5. doi: 10.1016/j.cub.2018.02.045. Epub 2018 Mar 22.
19: Maloney EM, Morrissey CA, Headley JV, Peru KM, Liber K. Can chronic exposure to imidacloprid, clothianidin, and thiamethoxam mixtures exert greater than additive toxicity in Chironomus dilutus? Ecotoxicol Environ Saf. 2018 Jul 30;156:354-365. doi: 10.1016/j.ecoenv.2018.03.003. Epub 2018 Mar 21. doi: 10.1016/j.foodchem.2018.02.061. Epub 2018 Feb 12.

合成参考文献


摘要:California Environmental Protection Agency/Department of Pesticide Regulation; Toxicology Data Review Summary for Thiamethoxam (153719-23-4) p.3 (September 4, 2008). Available from, as of May 25, 2011:
摘要:Meister, R.T., Sine, C; Crop Protection Handbook Volume 94. Meister Media Worldwide, Willoughby, OH 2008, p. D 424
摘要:California Environmental Protection Agency/Department of Pesticide Regulation; Toxicology Data Review Summary for Thiamethoxam (153719-23-4) p.13 (September 4, 2008). Available from, as of May 25, 2011:
摘要:Franke C et al; Chemosphere 29: 1501-14 (1994)
摘要:75 FR 35659 (6/23/2010)
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