CAS: 3598-13-8; 2-(4-Chlorophenoxy)Acetonitrile

该化合物是有机化合物,其特点是芳香结构和功能组;其特征是附属于苯氧基的氯联苯组,与丙酮类有关;该化合物一般是白色的,非白色的固体,以有机溶剂中的中度溶解性而著称;该化合物的特性使其在各种应用中有用,特别是在作为除草剂的农用化学化学品领域;氯化苯组的存在有助于其生物活动,而丙烯三烯组则加强其化学再活性. 4-丙烯三烯对合成有机化学也有兴趣,以其他化学实体的发展为目的.在处理该化合物时应考虑到安全因素,因为如果摄入或吸入,可能会对健康造成危害.适当的储存和处置方法对于减轻环境影响并确保实验室环境的安全至关重要.

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MSDS等安全信息

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上下游产品

CAS号107-14-2 氯乙腈 | CAS号106-48-9 对氯苯酚 | CAS号590-17-0 溴乙腈 | CAS号35368-44-6 2-(4-氯苯氧基)硫代乙酰胺 | CAS号43018-72-0 2-(4-chlorophen... | CAS号61756-69-2 p-chlorophenoxy... | CAS号111795-99-4 6-甲氧基-3-硝基吡啶-2-乙腈 | CAS号193629-32-2 2-[(4-chlorophe... | CAS号35368-44-6 2-(4-氯苯氧基)硫代乙酰胺 | CAS号3456-75-5 5-氟-2-硝基苯乙腈 | CAS号20876-27-1 (2-甲氧基-6-硝基苯基)乙腈 | CAS号105003-90-5 (4-甲氧基-2-硝基苯基)乙腈 | CAS号313233-24-8 (2-methoxy-4-ni... | CAS号17354-04-0 2-(4,5-二甲氧基-2-硝... | CAS号361456-00-0 3-硝基-6-[2-(三甲基甲... | CAS号3156-18-1 2-(4-Chloro-phe...

合成工艺路线路线简述

    📜P-Chlorophenoxyacetaldoxime置于乙酸酐体系中,化学反应生成 4-氯苯氧基乙腈
    参考文献:Khadse,B. G.; Lokhande,S. R.; Bhamaria,R. P.,Indian Journal Of Chemistry-Section B Organic And Medicinal Chemistry,1987,Vol. 26,# 1-12,P. 856-860
    标题:Khadse,B. G.; Lokhande,S. R.; Bhamaria,R. P.,Indian Journal Of Chemistry-Section B Organic And Medicinal Chemistry,1987,Vol. 26,# 1-12,P. 856-860

    海关参考信息

    专利信息


    专利号:AU-2007267799-A1
    优先权日:2006-05-25
    标 题 :Synthesis of a compound which is a suitable intermediate in the synthesis of oxindoledioxane derivatives

    专利号:AU-2007267799-B2
    优先权日:2006-05-25
    标 题 :Synthesis of a compound which is a suitable intermediate in the synthesis of oxindoledioxane derivatives

    专利号:ES-2387901-T3
    优先权日:2006-05-25
    标题 :Synthesis of a compound that is appropriate as an intermediate in the synthesis of oxindoledioxane derivatives

    专利号:CN-101448814-A
    优先权日:2006-05-25
    标 题:Synthesis of a compound which is a suitable intermediate in the synthesis of oxindoledioxane derivatives

    专利号:EP-2046771-B1
    优先权日:2006-05-25
    标 题:Synthesis of a compound which is suitable as intermediate in the synthesis of oxindoledioxane derivatives

    专利号:CN-101448814-B
    优先权日:2006-05-25
    标 题 :Synthesis of a compound which is a suitable intermediate in the synthesis of oxindoledioxane derivatives

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    合成参考文献


    摘要:Mérour, J.-Y.; Joseph, B., Science of Synthesis Knowledge Updates, (2016) 3, 141.
    摘要:Mérour, J.-Y.; Joseph, B., Science of Synthesis Knowledge Updates, (2017) 1, 271.
    摘要:Harris, P. A., Science of Synthesis Knowledge Updates, (2021) 3, 94.
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