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4,4-difluoro-1,3,5,7-tetramethyl-8-(3-thienyl)-4-bora-3a,4a-diaza-s-indacene | 1416913-29-5

中文名称
——
中文别名
——
英文名称
4,4-difluoro-1,3,5,7-tetramethyl-8-(3-thienyl)-4-bora-3a,4a-diaza-s-indacene
英文别名
5,5-Difluoro-1,3,7,9-tetramethyl-10-(3-thienyl)-5H-dipyrrolo[1,2-c:2 inverted exclamation mark,1 inverted exclamation mark-f][1,3,2]diazaborinin-4-ium-5-uide;2,2-difluoro-4,6,10,12-tetramethyl-8-thiophen-3-yl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-1(12),4,6,8,10-pentaene
4,4-difluoro-1,3,5,7-tetramethyl-8-(3-thienyl)-4-bora-3a,4a-diaza-s-indacene化学式
CAS
1416913-29-5
化学式
C17H17BF2N2S
mdl
——
分子量
330.209
InChiKey
XYOLIZGDQQENCV-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    4,4-difluoro-1,3,5,7-tetramethyl-8-(3-thienyl)-4-bora-3a,4a-diaza-s-indacene二甲基亚砜三氯氧磷 作用下, 以 二氯甲烷 为溶剂, 以20%的产率得到2-chloro-4,4-difluoro-1,3,5,7-tetramethyl-8-(3-thienyl)-4-bora-3a,4a-diaza-s-indacene-3-ium-4-ide
    参考文献:
    名称:
    The inorganic DMSO/POCl3 reaction with BODIPY: wide product formation and implications for biological ROS sensing and neurodegenerative disease research
    摘要:
    我们报告了用 POCl3/DMSO 处理 4,4-二氟-1,3,5,7-四甲基-8-(芳基)-4-bora-3a,4a-diaza-s-茚的精制和扩展合成研究。2-chloro-6-methylsulfide 衍生物(Kim TI、Park S、Choi Y 和 Kim Y. Chem. Asian J. 2011; 6: 1358-61.)是五种共助剂之一,其中包括 2,6-二磺酸基和二氯化物以及单取代的对应物。8-meso 尾基改变了产物的分布。不同的含硫产物在 NaOCl(10 等量)的作用下会产生不同的 "关闭-开启 "反应。化合物 4b 和 2b 显示出较低的毒性,并能进入神经母细胞瘤的并核区域。
    DOI:
    10.1142/s1088424612501180
  • 作为产物:
    描述:
    2,3-二氯-5,6-二氰基-1,4-苯醌三氟化硼乙醚三乙胺 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 16.0h, 以43 mg的产率得到4,4-difluoro-1,3,5,7-tetramethyl-8-(3-thienyl)-4-bora-3a,4a-diaza-s-indacene
    参考文献:
    名称:
    Meso-thienyl and furyl rotor effects in BF2-chelated dipyrrin dyes: solution spectroscopic studies and X-ray structural packing analysis of isomer and congener effects
    摘要:
    Well-defined discrete fluorescent molecular systems with very subtle steric/electronic differences are interesting when considering solid-state packing and solution substituent effects. Herein, we report the synthesis and characterization of four 4,4-difluoro-1,3,5,7-tetramethyl-8-(C4H3 X)-4-bora-3a,4a-diaza-s-indacene complexes (X?=?O, S). Various NMR spectroscopic experiments were used to assign all relevant atoms (CD2Cl2): 19F, 11B, 1H, 13C, 13CH undecoupled, 1H1H COSY, 1H1H NOESY, 1H13C HSQC, and 1H13C HMBC NMR spectroscopy. UV-Vis and fluorescence studies were undertaken for all compounds. Chemical shift differences were found between isomers and congeners; for congeners, aromatic d differences were attributed to electron-poor character. Also, compounds 14 were studied crystallographically. In the solid state, internal dihedral planes and intermolecular packing patterns can be compared.
    DOI:
    10.1080/00958972.2012.740023
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