CAS: 881685-58-1; Isopyrazam

该化合物是一种化学化合物,被归类为丙烯衍生物,主要被确认为在农业做法中用作杀真菌剂;它针对各种真菌病原体开展了广泛的活动,使其在作物保护方面很有价值;异丙拉萨姆的分子结构具有一种正促进其生物活动的双甲醇环;在标准环境条件下,它具有相对较低的波动性和稳定性,提高了其实地应用的功效;Isopyrazam通过一种独特的行动方式运作,它扰乱真菌细胞过程,导致抑制生长和繁殖;此外,必须指出,异丙拉萨姆经历了广泛的毒理学评估,以评价其对人类和非目标生物的安全性,导致若干地区的管制批准;与任何化学物质一样,适当处理和遵守安全准则对于减少使用该物质的潜在风险至关重要.

结构式图片

欧盟法规

REACH注册ECHA物质ECHA物质欧盟农药活性物质化妆品禁用物质清单C&L通报

上下游产品

1-methyl-3-(difluoromethyl)-1H-pyrazole-4-amide 5-chloro-9-isopropyl-1,2,3,4-tetrahydro-1,4-methano-naphthalene N-[1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]amine 4-bromo-3-(difluoromethyl)-1-methyl-1H-pyrazole

合成工艺路线路线简述

    📜9-Isopropylidene-5-Nitro-Benzonorbornene置于5% Rhodium-On-Charcoal Potassium Tert-Butylate,氢气体系中,用 四氢呋喃,氯苯 作为反应溶剂,化学反应 104.0H,反应生成 吡唑萘菌胺
    参考文献:Wo2007/31323
    标题:Wo2007/31323

    海关参考信息

    专利信息


    专利号:US-2022372000-A1
    优先权日:2021-05-05
    标 题:New Process for the Synthesis of 5-Fluoro-3-(Difuoromethyl)-5-Fluoro-1-Methyl-1H-Pyrazole-4-Carboxylic Acid Derivatives and the Free Acid Thereof
    发明人:LUO WEIFEN; WU WENTING
    权利人:FUJIAN YONGJING TECH CO LTD
    摘要:The invention provides a new process for the synthesis of 5-fluoro-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid derivatives and the free acid thereof, involving a direct fluorination reaction with a fluorination gas comprising or consisting of elemental fluorine (F2), in a reactor which is resistant to elemental fluorine (F2) and hydrogen fluoride (HF), and wherein in the process as a starting material a difluoromethyl-pyrazole compound dissolved in an inert solvent is subjected to the direct fluorination reaction. Some particular examples of 5-fluoro-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid derivatives which can be prepared according to the process of the invention are 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid fluoride (5F-DFMPAF), also known under the alternative name 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl fluoride; 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid ethylester (5F-DFMP); and 3-(chlorodifluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid ethylester (5F-CDFMP), or the corresponding methyl esters. The 5-fluoro-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid can be obtained from its carboxylic acid derivatives such as, e.g., mentioned before in that the acid derivative is converted to the corresponding carboxylic acid.

    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-2011230343-A1
    优先权日:2008-10-24
    标题 :Method for the Manufacture of Microparticles Comprising an Effect Substance
    发明人:SCHROERS MICHAEL; DYLLICK-BRENZINGER RAINER; MERK MICHAEL; BARG HEIKO
    权利人:BASF SE
    摘要:A subject matter of the present invention is a process for the preparation of effect compound-comprising microparticles M comprising A) the formation of a crude suspension of microparticles A by means of enzymatic polyester synthesis in an inverse miniemulsion comprising enzyme, effect compound and polyester monomers; and B) the polymerization of wall monomers from the group consisting of ethylenically unsaturated monomers, polyisocyanates and polyepoxides in the crude suspension of microparticles A. Furthermore, the present invention relates to microparticles M which can be obtained by means of the process according to the invention and also to an agrochemical formulation comprising microparticles M. In addition, the present invention relates to the use of microparticles M prepared according to the invention as component in colorants, cosmetics, drugs, biocides, plant protection agents, fertilizers, additives for food or animal fodder, or auxiliaries for polymers, paper, textiles, leather, detergents or cleaners. Finally, the invention also relates to a method for combating undesirable plant growth, to a method for combating undesirable insect or acarid infestation on plants and/or for combating phytopathogenic fungi, and to seeds treated with the agrochemical formulation.

    专利号:BR-112019014061-A2
    优先权日:2017-01-23
    标 题 :compounds of formula i, intermediates b, intermediates c, intermediates ii and intermediates d, composition, use, method to combat phytopathogenic fungi, seed and process for the synthesis of the compounds of formula i

    专利号:CN-108084093-A
    优先权日:2017-12-21
    标题:One-pot synthesis of 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid

    专利号:ES-2971524-T3
    优先权日:2010-09-01
    标 题 :Intermediates for the synthesis of fungicide pyrazoles

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:S132 | UJIGCAPCICCS | A GC-APCI-IMS-HRMS CCS Library from Izquierdo-Sandoval et al. (2022) | DOI:10.5281/zenodo.15831151
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