CAS: 202865-58-5; 1-Bromo-4,5-Difluoro-2-Methoxybenzene

该化合物是一种有机化合物,其特点是芳香结构,包括一个甲氧基组(-OCH3)和两个附于苯环的氟原子,以及一个溴替代物;该化合物是卤化厌氨衍生物的一部分,具有此类化合物的典型特性,包括药物和农用化学中的潜在应用;溴和氟原子的存在有助于其再活动,并可能影响其物理特性,如沸点和熔点,以及各种溶剂中的溶解性. 2-Bromo-4/5-二氟烷醇可能无色,其色度可能不至于黄黄色液体或固体,视其室温的状态而定.其分子结构表明,它可能参与电药性芳香替代反应,使其成为有机合成中有价值的中间体.在处理和储存时,应参考安全数据,因为卤化化合物可能对健康和环境造成风险.

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上下游产品

2-bromo-4,5-difluorophenol methyl iodide (4-amino-2-ethylsulfanylpyrimidin-5-yl)(2,3-difluoro-6-methoxyphenyl)methanone (4-amino-2-ethylsulfanylpyrimidin-5-yl)(4,5-difluoro-2-methoxyphenyl)methanone N,O-dimethylhydroxylamine*hydr°Chloride [2-(4,5-difluoro-2-methoxy-phenyl)-6-methoxy-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone

合成工艺路线路线简述

    📜2-溴-4,5-二氟苯酚,碘甲烷置于potassium Carbonate体系中,用 N,N-二甲基甲酰胺 用作溶剂,化学反应 4.0H,以1.16 G的收率获得2-溴-4,5-二氟苯甲醚
    参考文献: Novel Tetrahydropyridopyrimidines And Tetrahydropyridopyridines For The Treatment And Prophylaxis Of Hepatitis B Virus Infection[fr] Nouvelles Tétrahydropyridopyrimidines Et Tétrahydropyridopyridines Pour Le Traitement Et La Prévention D'Une Infection Par Le Virus De L'Hépatite B
    标题: Novel Tetrahydropyridopyrimidines And Tetrahydropyridopyridines For The Treatment And Prophylaxis Of Hepatitis B Virus Infection[fr] Nouvelles Tétrahydropyridopyrimidines Et Tétrahydropyridopyridines Pour Le Traitement Et La Prévention D'Une Infection Par Le Virus De L'Hépatite B
    摘要:这项发明提供了具有一般式(i)的新化合物:其中r1,R2,R3,Q,U,W,Z,X和y如本文所述,包括这些化合物的组合物以及使用这些化合物的方法.这些化合物是hbsag抑制剂,可用作治疗或预防hbv感染的药物.

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    专利信息


    专利号:US-7615634-B2
    优先权日:2003-02-10
    标题:4-aminopyrimidine-5-one derivatives
    发明人:BARTKOVITZ DAVID JOSEPH; CHU XIN-JIE; DING QINGJIE; JIANG NAN; LOVEY ALLEN JOHN; MOLITERNI JOHN ANTHONY; MULLIN JR JOHN GUILFOYLE; VU BINH THANH; WOVKULICH PETER MICHAEL
    权利人:HOFFMANN LA ROCHE
    摘要:Novel intermediate compounds are disclosed. These compounds are useful in the synthesis of 4-aminopyrimidine-5-one derivatives that inhibit cyclin-dependent kinases, in particular cyclin-dependent kinase 4 (Cdk4). The 4-aminopyrimidine-5-one derivatives and their pharmaceutically acceptable salts have antiproliferative activity and are useful in the treatment or control of cancer, in particular solid tumors.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Ruthenium-Catalyzed Site-Selective Intramolecular Silylation Of Primary C-H Bonds For Synthesis Of Sila-Heterocycles
    作者:Huaquan Fang,Wenjun Hou,Guixia Liu,Zheng Huang |发布日期:2017.8.23
    摘要:Medicinal Chemistry. Moreover, Organosilanes Are Valuable Synthetic Intermediates For Fine Chemicals And Materials. Transition Metal-Catalyzed C-H Silylation Has Become An Important Strategy For C-Si Bond Formations. However, Despite The Great Advances In Aromatic C(Sp2)-H Bond Silylations, Catalytic Methods For Aliphatic C(Sp3)-H Bond Silylations Are Relatively Rare. Here We Report A Pincer Ruthenium
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