CAS: 144432-85-9; 3-Chloro-4-Fluorophenylboronic Acid

该化合物是一种有机体化合物,其特征是附在一个联苯环上的碱酸功能组,以氯和氟原子替代氯和氟原子,这种化合物一般是白色的,白色为非白固体,可溶于水和酒精等极地溶剂,因为乙酸组,这种化合物的分子结构具有一个苯环,其元体位置为氯原子,氟原子相对于卤酸组处于准位置.这些卤素子体的存在会影响该化合物的再活动性及其参与各种化学反应的能力,例如铃木结合,这种结合在有机合成和药用化学中具有重大意义.此外,人们知道丁醇酸能够与二醇形成可逆转的复合体,使其在各种应用中有用,包括药物开发和材料科学.该化合物的独特特性使它成为合成药物和农用化学物的一个有价值的中间体.

结构式图片

相似化合物

635305-46-3 850623-59-5 1646614-31-4

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CAS号60811-21-4 4-溴-2-氯-1-氟苯 | CAS号175883-06-4 2-chloro-1-fluo... | CAS号923567-82-2 3-(3-chloro-4-f...

合成工艺路线路线简述

    3-氯-4-氟溴苯置于正丁基锂,硼酸三异丙酯体系中,用 四氢呋喃,正己烷,甲苯 用作溶剂,以86%的收率获得3-氯-4-氟苯硼酸
    参考文献:用于制备3-吡啶基-和一些芳基硼酸的改进方案.
    标题:用于制备3-吡啶基-和一些芳基硼酸的改进方案.
    摘要:通过锂-卤素交换和"原位猝灭"的方案,由3-溴吡啶以高产率和大量制备3-吡啶基硼酸.在制备芳基硼酸时,对该技术进行了进一步的研究并在其他芳基卤化物上进行了评估.
    Doi:10.1021/jo025792P

    海关参考信息

    专利信息


    专利号:US-2024215280-A1
    优先权日:2022-10-31
    标 题:In situ core/shell perovskite nanocrystal material, method of preparation thereof, and light emitting device comprising the same
    发明人:LEE TAE-WOO; KIM JOO SUNG
    权利人:SEOUL NAT UNIV R&DB FOUNDATION; PEROLED CO LTD
    摘要:The present inventive concept relates to an in situ core/shell perovskite nanocrystal film formed by an in situ nanocrystal synthesis process, a method for producing the same, and a light emitting device comprising the same as a light-emitting layer. The in situ core/shell perovskite nanocrystal film formed by the in situ nanocrystal synthesis process according to the present inventive concept exhibits a strong charge confinement effect by nanocrystal formation, and can simultaneously greatly improve the luminescence efficiency and lifetime by maintaining the fast charge transport capability of polycrystalline perovskite.

    专利号:US-7781470-B2
    优先权日:1999-09-13
    标题:Aminodicarboxylic acid derivatives having pharmaceutical properties
    发明人:ALONSO-ALIJA CRISTINA; HEIL MARKUS; FLUBACHER DIETMAR; NAAB PAUL; PERNERSTORFER JOSEF; STASCH JOHANNES-PETER; WUNDER FRANK; DEMBOWSKY KLAUS; PERZBORN ELIZABETH; STAHL ELKE
    权利人:BAYER SCHERING PHARMA AG
    摘要:The invention relates to compounds of formulae (II), (IV), and (VI) as shown below, n nwherein the several variable groups are as defined in the specification and claims. Processes for making these materials, and methods for using them in the synthesis of compounds for treatment of cardiovascular disorders and fibrotic disorders are also disclosed.

    专利号:US-2024158692-A1
    优先权日:2022-10-31
    标题 :In-situ core/shell nanoparticle structured metal halide perovskite luminescent material, light emitting device including the same, and manufacturing method thereof
    发明人:LEE TAE-WOO; KIM JOO SUNG
    权利人:SEOUL NAT UNIV R&DB FOUNDATION; PEROLED CO LTD
    摘要:The present inventive concept relates to an in situ core/shell perovskite nanocrystal film formed by an in situ nanocrystal synthesis process, a method for producing the same, and a light emitting device comprising the same as a light-emitting layer. The in situ core/shell perovskite nanocrystal film formed by the in situ nanocrystal synthesis process according to the present inventive concept exhibits a strong charge confinement effect by nanocrystal formation, and can simultaneously greatly improve the luminescence efficiency and lifetime by maintaining the fast charge transport capability of polycrystalline perovskite.

    专利号:US-7671085-B2
    优先权日:2002-11-15
    标 题 :Non-steroidal farnesoid X receptor modulators and methods for the use thereof
    发明人:DOWNES MICHAEL R; EVANS RONALD M
    权利人:SALK INST FOR BIOLOGICAL STUDI
    摘要:The efficient regulation of cholesterol synthesis, metabolism, acquisition, and transport is an essential component of lipid homeostasis. The farnesoid X receptor (FXR) is a transcriptional sensor for bile acids, the primary product of cholesterol metabolism. Accordingly, the development of potent, selective, small molecule agonists, partial agonists, and antagonists of FXR would be an important step in further deconvoluting FXR physiology. In accordance with the present invention, the identification of novel potent FXR activators is described. Two derivatives of invention compounds, bearing stilbene or biaryl moieties, contain members that are the most potent FXR agonists reported to date in cell-based assays. These compounds are useful as chemical tools to further define the physiological role of FXR as well as therapeutic leads for the treatment of diseases linked to cholesterol, bile acids and their metabolism and homeostasis.

    专利号:US-9951062-B2
    优先权日:2012-12-14
    标 题 :Substituted 1 H-pyrrolo [2, 3-b] pyridine and 1 H-pyrazolo [3, 4-b] pyridine derivatives as salt inducible kinase 2 (SIK2) inhibitors
    发明人:VANKAYALAPATI HARIPRASAD; YERRAMREDDY VENKATAKRISHNAREDDY; GANIPISETTY VENU BABU; TALLURI SURESHKUMAR; APPALANENI RAJENDRA P
    权利人:ARRIEN PHARMACEUTICALS LLC
    摘要:Compounds according to Formulas I, IA or IB: n nto pharmaceutically acceptable composition, salts thereof, their synthesis and their use as SIK2 inhibitors including such compounds and methods of using said compounds in the treatment of various diseases and/or disorders such as cancer, stroke, cardiovascular, obesity and type II diabetes.

    专利号:US-9856241-B2
    优先权日:2013-07-03
    标 题:Substituted benzofuranyl and benzoxazolyl compounds and uses thereof
    发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM; MCCAULEY DILARA; LANDESMAN YOSEF; GOLAN GALI; KALID ORI; SHECHTER SHARON
    权利人:KARYOPHARM THERAPEUTICS INC
    摘要:The invention generally relates to substituted benzofuranyl and substituted benzoxazolyl compounds, and more particularly to a compound represented by Structural Formula (A): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of Structural Formula (A), or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders.
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    合成参考文献


    摘要:Miyaura, N., Science of Synthesis, (2005) 6, 296.
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