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5-(4-Hydroxybut-1-ynyl)-6-(2-hydroxyethyl)dec-5-en-3,7-diyne-1,10-diol | 1579287-14-1

中文名称
——
中文别名
——
英文名称
5-(4-Hydroxybut-1-ynyl)-6-(2-hydroxyethyl)dec-5-en-3,7-diyne-1,10-diol
英文别名
5-(4-hydroxybut-1-ynyl)-6-(2-hydroxyethyl)dec-5-en-3,7-diyne-1,10-diol
5-(4-Hydroxybut-1-ynyl)-6-(2-hydroxyethyl)dec-5-en-3,7-diyne-1,10-diol化学式
CAS
1579287-14-1
化学式
C16H20O4
mdl
——
分子量
276.332
InChiKey
DVXJYSJNRLNDLE-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):
    0.9
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    80.9
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-丁炔-1-醇 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide正丁胺 作用下, 以 为溶剂, 反应 0.75h, 以30%的产率得到
    参考文献:
    名称:
    Palladium(II)–copper(I) mediated homotrimerization and homotetramerization of terminal alkynes
    摘要:
    Alkyne homocoupling is commonly observed in cross coupling reactions; however, self trimerization and homotetramerization of alkynes to form branched products through cross-coupling reactions are rarely reported. We describe herein homotrimerization and homotetramerization of terminal alkynes under the Sonogashira reaction conditions that gave the corresponding modified enediynes. Substrate scope for this reaction was explored. (c) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2014.01.146
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文献信息

  • Palladium(II)–copper(I) mediated homotrimerization and homotetramerization of terminal alkynes
    作者:Ravi Shekar Yalagala、Ningzhang Zhou、Hongbin Yan
    DOI:10.1016/j.tetlet.2014.01.146
    日期:2014.3
    Alkyne homocoupling is commonly observed in cross coupling reactions; however, self trimerization and homotetramerization of alkynes to form branched products through cross-coupling reactions are rarely reported. We describe herein homotrimerization and homotetramerization of terminal alkynes under the Sonogashira reaction conditions that gave the corresponding modified enediynes. Substrate scope for this reaction was explored. (c) 2014 Elsevier Ltd. All rights reserved.
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