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| 1044141-10-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1044141-10-7
化学式
C16H24O5
mdl
——
分子量
296.364
InChiKey
QJFFHGNXPTZWQN-OZGPGHLVSA-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):
    1.79
  • 重原子数:
    21.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    64.99
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    二异丁基氢化铝 作用下, 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Synthesis of BC-ring model of globostellatic acid X methyl ester, an anti-angiogenic substance from marine sponge
    摘要:
    Concise synthesis of BC-ring model compounds of 13E, 17E-globostellatic acid X methyl ester, an anti-angiogenic triterpene derivative from Indonesian marine sponge, was achieved through ynolate olefination and allylic oxidation as key steps. The model compound 5, which was synthesized within 10 reaction steps from commercially available Hajos-Parrish ketone, showed anti-proliferative activity against HUVECs with moderate selectivity. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.05.018
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis of BC-ring model of globostellatic acid X methyl ester, an anti-angiogenic substance from marine sponge
    摘要:
    Concise synthesis of BC-ring model compounds of 13E, 17E-globostellatic acid X methyl ester, an anti-angiogenic triterpene derivative from Indonesian marine sponge, was achieved through ynolate olefination and allylic oxidation as key steps. The model compound 5, which was synthesized within 10 reaction steps from commercially available Hajos-Parrish ketone, showed anti-proliferative activity against HUVECs with moderate selectivity. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.05.018
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