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4-(2,5-bis-hexyloxy-4-{4-[(triisopropylsilanyl)-ethynyl]-phenylethynyl}phenyl)-but-3-yn-2-ol | 946073-21-8

中文名称
——
中文别名
——
英文名称
4-(2,5-bis-hexyloxy-4-{4-[(triisopropylsilanyl)-ethynyl]-phenylethynyl}phenyl)-but-3-yn-2-ol
英文别名
4-[2,5-Dihexoxy-4-[2-[4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]-2-methylbut-3-yn-2-ol;4-[2,5-dihexoxy-4-[2-[4-[2-tri(propan-2-yl)silylethynyl]phenyl]ethynyl]phenyl]-2-methylbut-3-yn-2-ol
4-(2,5-bis-hexyloxy-4-{4-[(triisopropylsilanyl)-ethynyl]-phenylethynyl}phenyl)-but-3-yn-2-ol化学式
CAS
946073-21-8
化学式
C42H60O3Si
mdl
——
分子量
641.022
InChiKey
ZBPNPPCAAXBZTM-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):
    10.7
  • 重原子数:
    46
  • 可旋转键数:
    21
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-(2,5-bis-hexyloxy-4-{4-[(triisopropylsilanyl)-ethynyl]-phenylethynyl}phenyl)-but-3-yn-2-ol 在 tris(dibenzylideneacetone)dipalladium (0) sodium hydroxidecopper(l) iodide四丁基氟化铵三乙胺三苯基膦 作用下, 以 四氢呋喃氯仿甲苯 为溶剂, 反应 120.0h, 生成 N-(4-((4-((4-((4-ethynyl-2,5-bis(hexyloxy)phenyl)ethynyl)phenyl)ethynyl)-2,5-bis(hexyloxy)phenyl)ethynyl)phenyl)formamide
    参考文献:
    名称:
    An effective, orthogonal deprotection strategy for differentially functionalized, linear and Y-shaped oligo phenylene ethynylenes
    摘要:
    Several methodologies for the selective deprotection acetylenes have been reported previously. However, as is shown here, they are often not reliable or convenient. Here, an approach is reported that is efficient and general. Use of this approach to synthesize several two- and three-armed oligo(phenylene ethynylene) molecules with differentiated end groups is reported. In addition, preliminary characterization of the fluorescent properties of some of these molecules and their ability to form self-assembled monolayers (SAMs) is reported. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.05.006
  • 作为产物:
    描述:
    参考文献:
    名称:
    An effective, orthogonal deprotection strategy for differentially functionalized, linear and Y-shaped oligo phenylene ethynylenes
    摘要:
    Several methodologies for the selective deprotection acetylenes have been reported previously. However, as is shown here, they are often not reliable or convenient. Here, an approach is reported that is efficient and general. Use of this approach to synthesize several two- and three-armed oligo(phenylene ethynylene) molecules with differentiated end groups is reported. In addition, preliminary characterization of the fluorescent properties of some of these molecules and their ability to form self-assembled monolayers (SAMs) is reported. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.05.006
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文献信息

  • An effective, orthogonal deprotection strategy for differentially functionalized, linear and Y-shaped oligo phenylene ethynylenes
    作者:Kusum L. Chandra、Sheng Zhang、Christopher B. Gorman
    DOI:10.1016/j.tet.2007.05.006
    日期:2007.7
    Several methodologies for the selective deprotection acetylenes have been reported previously. However, as is shown here, they are often not reliable or convenient. Here, an approach is reported that is efficient and general. Use of this approach to synthesize several two- and three-armed oligo(phenylene ethynylene) molecules with differentiated end groups is reported. In addition, preliminary characterization of the fluorescent properties of some of these molecules and their ability to form self-assembled monolayers (SAMs) is reported. (C) 2007 Elsevier Ltd. All rights reserved.
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