摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

ethyl (trans)-10-(trimethylsilyl)dec-4-en-9-ynoate | 628687-58-1

中文名称
——
中文别名
——
英文名称
ethyl (trans)-10-(trimethylsilyl)dec-4-en-9-ynoate
英文别名
ethyl (E)-10-trimethylsilyldec-4-en-9-ynoate
ethyl (trans)-10-(trimethylsilyl)dec-4-en-9-ynoate化学式
CAS
628687-58-1
化学式
C15H26O2Si
mdl
——
分子量
266.456
InChiKey
UKRLEVSKTRCFLR-VQHVLOKHSA-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:
    296.7±33.0 °C(Predicted)
  • 密度:
    0.911±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.94
  • 重原子数:
    18
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    ethyl (trans)-10-(trimethylsilyl)dec-4-en-9-ynoate 在 bis-triphenylphosphine-palladium(II) chloride AD-mix-α 、 copper(l) iodide甲基磺酰胺四丁基氟化铵三乙胺 作用下, 以 四氢呋喃叔丁醇 为溶剂, 反应 53.0h, 生成 (5R)-3-[(S)-13-hydroxy-13-((S)-5-oxotetrahydrofuran-2-yl)tridec-6-en-8-ynyl]-5-methyl-3-(phenylsulfanyl)dihydrofuran-2-one
    参考文献:
    名称:
    Design, syntheses, and biological evaluations of squamostolide and its related analogs
    摘要:
    Squamostolide and its related analogs were designed and synthesized for biological evaluation. All these compounds were tested for growth inhibition activities against human tumor cell lines, in which one of the compounds showed the most potent cyto-toxicity among these derivatives against a full panel of 60 human cancer cell lines. The same compound also showed G2/M phase arrest and a weak apoptotic effect during flow cytometric analysis. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.05.050
  • 作为产物:
    参考文献:
    名称:
    Synthesis of (15S,16S,21R)-4-deoxyrollicosin analog
    摘要:
    Synthesis of 4-deoxy rollicosin analog 2 was completed in nine steps, which was based on palladium-catalyzed coupling of two building blocks 3 and 4. Lactone 3 was synthesized from 5-hexyn-1-ol, and vinyl iodide 4 was accessed from L-glutamate and 1-hexyne. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.08.088
点击查看最新优质反应信息

文献信息

  • Synthesis of (15S,16S,21R)-4-deoxyrollicosin analog
    作者:Jeng-Lin Lee、Chi-Fong Lin、Ling-Yu Hsieh、Wan-Ru Lin、Huey-Fen Chiu、Yang-Chang Wu、Kun-Sheng Wang、Ming-Jung Wu
    DOI:10.1016/j.tetlet.2003.08.088
    日期:2003.10
    Synthesis of 4-deoxy rollicosin analog 2 was completed in nine steps, which was based on palladium-catalyzed coupling of two building blocks 3 and 4. Lactone 3 was synthesized from 5-hexyn-1-ol, and vinyl iodide 4 was accessed from L-glutamate and 1-hexyne. (C) 2003 Elsevier Ltd. All rights reserved.
  • Design, syntheses, and biological evaluations of squamostolide and its related analogs
    作者:Cheng-Lin Lee、Chi-Fong Lin、Wan-Ru Lin、Kun-Sheng Wang、Ya-her Chang、Shinne-Ren Lin、Yang-Chang Wu、Ming-Jung Wu
    DOI:10.1016/j.bmc.2005.05.050
    日期:2005.10
    Squamostolide and its related analogs were designed and synthesized for biological evaluation. All these compounds were tested for growth inhibition activities against human tumor cell lines, in which one of the compounds showed the most potent cyto-toxicity among these derivatives against a full panel of 60 human cancer cell lines. The same compound also showed G2/M phase arrest and a weak apoptotic effect during flow cytometric analysis. (c) 2005 Elsevier Ltd. All rights reserved.
查看更多