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1,1,3,3-tetramethyl-1,3-dihydronaphtho[2,3-c][1,2,5]oxadisilole-6,7-dicarbaldehyde | 1013662-53-7

中文名称
——
中文别名
——
英文名称
1,1,3,3-tetramethyl-1,3-dihydronaphtho[2,3-c][1,2,5]oxadisilole-6,7-dicarbaldehyde
英文别名
——
1,1,3,3-tetramethyl-1,3-dihydronaphtho[2,3-c][1,2,5]oxadisilole-6,7-dicarbaldehyde化学式
CAS
1013662-53-7
化学式
C16H18O3Si2
mdl
——
分子量
314.488
InChiKey
NNLJWJICNYBLDL-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):
    2.32
  • 重原子数:
    21.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,1,3,3-tetramethyl-1,3-dihydronaphtho[2,3-c][1,2,5]oxadisilole-6,7-dicarbaldehyde1,4-环己二酮氢氧化钾 作用下, 以 乙醇 为溶剂, 以96%的产率得到10,10,12,12,28,28,30,30-Octamethyl-11,29-dioxa-10,12,28,30-tetrasilanonacyclo[19.15.0.03,19.05,17.07,15.09,13.023,35.025,33.027,31]hexatriaconta-1(36),3,5,7,9(13),14,16,18,21,23,25,27(31),32,34-tetradecaene-2,20-dione
    参考文献:
    名称:
    Oxadisilole fused pentacenequinones and heptacenequinones
    摘要:
    Stable, organic solvent soluble bis- and tetrakis-oxadisilole fused pentacenequinones (5a - b) and heptacenequinones (11a - b) were synthesized. Double Diels - Alder and fourfold aldol-condensation approaches were used. Absorption, emission and fluorescence quantum yield of the previously unknown acenequinones 5a and 11a were characterized. The role of the oxadisilole substituent on the photophysical properties was addressed. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.11.164
  • 作为产物:
    描述:
    草酰氯二甲基亚砜三乙胺 作用下, 以 二氯甲烷 为溶剂, 以84%的产率得到1,1,3,3-tetramethyl-1,3-dihydronaphtho[2,3-c][1,2,5]oxadisilole-6,7-dicarbaldehyde
    参考文献:
    名称:
    Oxadisilole fused pentacenequinones and heptacenequinones
    摘要:
    Stable, organic solvent soluble bis- and tetrakis-oxadisilole fused pentacenequinones (5a - b) and heptacenequinones (11a - b) were synthesized. Double Diels - Alder and fourfold aldol-condensation approaches were used. Absorption, emission and fluorescence quantum yield of the previously unknown acenequinones 5a and 11a were characterized. The role of the oxadisilole substituent on the photophysical properties was addressed. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.11.164
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