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9-[4-(3-Formylphenanthren-9-yl)butyl]phenanthrene-3-carbaldehyde | 862305-60-0

中文名称
——
中文别名
——
英文名称
9-[4-(3-Formylphenanthren-9-yl)butyl]phenanthrene-3-carbaldehyde
英文别名
9-[4-(3-formylphenanthren-9-yl)butyl]phenanthrene-3-carbaldehyde
9-[4-(3-Formylphenanthren-9-yl)butyl]phenanthrene-3-carbaldehyde化学式
CAS
862305-60-0
化学式
C34H26O2
mdl
——
分子量
466.579
InChiKey
QTMLUJPLLHCBHA-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:
    729.3±40.0 °C(Predicted)
  • 密度:
    1.241±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    9.1
  • 重原子数:
    36
  • 可旋转键数:
    7
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    9-[4-(3-Formylphenanthren-9-yl)butyl]phenanthrene-3-carbaldehyde 在 sodium tetrahydroborate 、 4-甲基苯磺酸吡啶 作用下, 以 乙醇1,2-二氯乙烷 为溶剂, 生成 6-Oxaheptacyclo[22.7.1.14,31.18,12.111,19.013,18.025,30]pentatriaconta-1(31),2,4(33),8(35),9,11,13,15,17,19(34),24(32),25,27,29-tetradecaene
    参考文献:
    名称:
    Synthesis and Fluorescence Spectra of Oxa[3.n]phenanthrenophanes
    摘要:
    Novel photostable oxa[3.n](3,9)- and (3.3](3,10)phenanthrenophanes (n = 3, 4) bearing trimethylene-type linkage(s) were successfully synthesized by the intramolecular acid-catalyzed etherification of the corresponding precursor diols. syn-Oxa[3.3](3,10)phenanthrenophane afforded the most red-shifted excimer fluorescence (lambda(max) = 432 nm) among the phenanthrenophanes so far prepared.
    DOI:
    10.1021/ol051047y
  • 作为产物:
    描述:
    哌啶-1-甲醛 、 3-Bromo-9-[4-(3-bromophenanthren-9-yl)butyl]phenanthrene 在 正丁基锂 作用下, 以 四氢呋喃 为溶剂, 以41%的产率得到9-[4-(3-Formylphenanthren-9-yl)butyl]phenanthrene-3-carbaldehyde
    参考文献:
    名称:
    Synthesis and Fluorescence Spectra of Oxa[3.n]phenanthrenophanes
    摘要:
    Novel photostable oxa[3.n](3,9)- and (3.3](3,10)phenanthrenophanes (n = 3, 4) bearing trimethylene-type linkage(s) were successfully synthesized by the intramolecular acid-catalyzed etherification of the corresponding precursor diols. syn-Oxa[3.3](3,10)phenanthrenophane afforded the most red-shifted excimer fluorescence (lambda(max) = 432 nm) among the phenanthrenophanes so far prepared.
    DOI:
    10.1021/ol051047y
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文献信息

  • Synthesis and Fluorescence Spectra of Oxa[3.<i>n</i>]phenanthrenophanes
    作者:Yosuke Nakamura、Takuzo Yamazaki、Jun Nishimura
    DOI:10.1021/ol051047y
    日期:2005.7.1
    Novel photostable oxa[3.n](3,9)- and (3.3](3,10)phenanthrenophanes (n = 3, 4) bearing trimethylene-type linkage(s) were successfully synthesized by the intramolecular acid-catalyzed etherification of the corresponding precursor diols. syn-Oxa[3.3](3,10)phenanthrenophane afforded the most red-shifted excimer fluorescence (lambda(max) = 432 nm) among the phenanthrenophanes so far prepared.
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