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2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole | 1021919-38-9

中文名称
——
中文别名
——
英文名称
2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole
英文别名
2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1H-benzimidazole
2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole化学式
CAS
1021919-38-9
化学式
C19H21BN2O2
mdl
——
分子量
320.199
InChiKey
VKTQVXBRQSBBLU-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.53
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    47.1
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Halogen-Bonding-Promoted Photoinduced C–X Borylation of Aryl Halide Using Phenol Derivatives
    作者:Kazuki Matsuo、Eiji Yamaguchi、Akichika Itoh
    DOI:10.1021/acs.joc.3c00201
    日期:2023.5.5
    photoinduced C–X borylation reaction of aryl halides by forming a halogen-bonding (XB) complex using 2-naphthol as an XB acceptor. The method is chemoselective and broadly functional group tolerant and provides concise access to corresponding boronate esters. Mechanistic studies reveal that forming the XB complex between aryl halide and naphthol acts as an electron donor–acceptor complex to furnish aryl radicals
    本研究通过使用 2-萘酚作为 XB 受体形成卤素键合 (XB) 络合物来研究芳基卤化物的光诱导 C-X 硼化反应。该方法具有化学选择性和广泛的官能团耐受性,并提供了获得相应硼酸酯的简明途径。机理研究表明,在芳基卤化物和萘酚之间形成 XB 络合物作为电子供体-受体络合物,通过光诱导电子转移提供芳基自由基。
  • <b>Unprecedented Small Molecule-Based Uniform Two-Dimensional Platelets with Tailorable Shapes and Sizes</b>
    作者:Yanjun Gong、Chuanqin Cheng、Hongwei Ji、Yanke Che、Ling Zang、Jincai Zhao、Yifan Zhang
    DOI:10.1021/jacs.2c07480
    日期:2022.8.24
  • WO2008/51493
    申请人:——
    公开号:——
    公开(公告)日:——
  • Light‐Regulated Nucleation for Growing Highly Uniform Single‐Crystalline Microrods
    作者:Lishan Sun、Yanjun Gong、Yanxue Che、Hongwei Ji、Bing Liu、Yanke Che、Jincai Zhao
    DOI:10.1002/anie.202402253
    日期:——
    Abstract

    We report a light‐irradiation method to control the synchronous nucleation of a donor‐acceptor (D‐A) fluorophore for growing highly uniform single‐crystalline microrods, which is in sharp contrast to the prevailing methods of restricting spontaneous nucleation and additionally adding seeds. The D‐A fluorophore was observed to undergo photoinduced electron transfer to CrCl3, leading to the generation of HCl and the subsequent protonation of the D‐A fluorophore. By intensifying photoirradiation or prolonging its duration, the concentration of protonated D‐A fluorophores can be rapidly increased to a high supersaturation level. This results in the formation of a controlled number of nuclei in a synchronous manner, which in turn kickstart the epitaxial growth of protonated D‐A fluorophores towards uniform single‐crystalline microrods of controlled sizes. The light‐regulated synchronous nucleation and uniform growth of microrods are a unique phenomenon that can only be achieved by specific Lewis acids, making it a novel probing method for sensitively detecting strong Lewis acids such as chromium chloride.

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