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2-(2-(methoxymethoxy)naphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 1384055-50-8

中文名称
——
中文别名
——
英文名称
2-(2-(methoxymethoxy)naphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
英文别名
4,4,5,5-tetramethyl-2-[2-(methoxymethoxy)naphthalen-1-yl]-1,3,2-dioxaborolane;2-[2’-(methoxymethoxy)naphthalen-1’-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;1-(2-methoxymethoxynaphth-1-yl)pinacolborane;2-[2-(Methoxymethoxy)naphthalen-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-(2-(methoxymethoxy)naphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane化学式
CAS
1384055-50-8
化学式
C18H23BO4
mdl
——
分子量
314.189
InChiKey
UWJIPUCCCZMVRI-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    452.4±30.0 °C(Predicted)
  • 密度:
    1.10±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.12
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Tris(spiroborate)‐Type Anionic Nanocycles
    作者:Hiroshi Danjo、Natsuyo Mitani、Yusuke Muraki、Masatoshi Kawahata、Isao Azumaya、Kentaro Yamaguchi、Toshifumi Miyazawa
    DOI:10.1002/asia.201200162
    日期:2012.7
    Full circle: New cyclic tris(spiroborate)s were prepared as molecular recognition modules for nanometer‐sized cationic guests. These cyclophanes were simply prepared by treating corresponding bis(2,3‐dihydroxynaphthalene)s with an equimolar amount of boric acid. The molecular recognition ability of these cyclic spiroborates was estimated in solution and crystal phases by the use of [Ir(tpy2)]3+ as
    整圈:制备了新的环状三(螺硼酸酯)作为纳米级阳离子客体的分子识别模块。通过用等摩尔量的硼酸处理相应的双(2,3-二羟基萘),可以简单地制备这些环烷。通过使用[Ir(tpy 2)] 3+作为阳离子客体的典型实例,评估了在溶液相和结晶相中这些环状螺硼酸酯的分子识别能力。
  • Nestable Tetrakis(spiroborate) Nanocycles
    作者:Hiroshi Danjo、Yuhki Hashimoto、Yuki Kidena、Ayumi Nogamine、Kosuke Katagiri、Masatoshi Kawahata、Toshifumi Miyazawa、Kentaro Yamaguchi
    DOI:10.1021/acs.orglett.5b00747
    日期:2015.5.1
    Multicomponent construction of the tetrakis(spiroborate) anionic nanocycles was achieved by reacting bis(dihydroxynaphthalene)s with tetrahydroxyanthraquinone in the presence of boric acid in a self-organized manner. These nanocycles exhibited selective molecular recognition behavior toward cationic guests such as methyl viologen derivatives. Formation of a supramolecular [email protected] and a [
    通过使双(二羟基)与四羟基蒽醌硼酸存在下以自组织方式反应,实现了四(螺硼酸酯)阴离子纳米环的多组分构建。这些纳米环表现出对阳离子客体如甲基紫精生物的选择性分子识别行为。通过结合阴离子纳米环和环双(百草枯-对苯撑)的乙烯基类似物,观察到超分子[受电子邮件保护]和[受电子邮件保护]环结构的形成。
  • Confronting the Challenge of Asymmetric Carbonyl Addition to Sterically Bulky Isatins: Upgrading Dirhodium(II)/Biphosphine Catalytic System
    作者:Wenjing Guo、Shuming Zhan、Han Yang、Zhenhua Gu
    DOI:10.1021/acs.orglett.3c01028
    日期:2023.5.12
    Catalytic asymmetric addition of arylboronic acids to ketones is a powerful transformation for directly delivering chiral tertiary alcohols. However, there is no successful example of enantioselective addition to steric bulky isatins, which contain bulky substituent at the 4-position. To confront this challenge, in this work a dirhodium/(BTFM-Garphos) system was developed that showed extremely high
    将芳基硼酸催化不对称加成到酮是一种直接提供手性叔醇的强大转化。然而,没有成功的对映选择性加成到空间庞大的靛红,其中在 4 位包含庞大的取代基。为了应对这一挑战,在这项工作中开发了二/(BTFM-Garphos) 系统,该系统显示出极高的活性和立体选择性,反应通常在几分钟内完成。
  • Economical and Readily Accessible Preparation of <i>o</i>,<i>o</i>-Disubstituted Arylboronates through Palladium-Catalyzed Borylation of Haloarenes
    作者:Ryoichi Kuwano、Eunhyung Lee、Sungyong Won
    DOI:10.1021/acs.orglett.1c03926
    日期:2021.12.17
  • Selective detection of Cys and GSH by using one fluorescent probe at two excitation wavelengths
    作者:Yintang Xiao、Kai Guo、Jun Wei、Xiaowei Gao、Dong Yi、Yang Li、Xiaoqi Yu、Chun Zhang、Qin Wang
    DOI:10.1016/j.tetlet.2020.152462
    日期:2020.10
    Selective detection of Cys and GSH by using one fluorescent probe with two different excitation wavelengths is developed based on a naphthyl-coumarin aldehyde probe. Mechanistic studies indicate that the distinctively different fluorescent responses of the probe toward Cys and GSH at the two excitation wavelengths are due to two different reaction pathways that generate different products. The probe has been used to detect Cys and GSH in HeLa cells by using two emission channels. (C) 2020 Elsevier Ltd. All rights reserved.
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