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2-乙酰氧基十六烷酸乙酯 | 260055-66-1

中文名称
2-乙酰氧基十六烷酸乙酯
中文别名
——
英文名称
Ethyl 2-acetyloxyhexadecanoate
英文别名
——
2-乙酰氧基十六烷酸乙酯化学式
CAS
260055-66-1
化学式
C20H38O4
mdl
——
分子量
342.519
InChiKey
IRKUIUTXOXLLGW-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

物化性质

  • 沸点:
    415.0±18.0 °C(Predicted)
  • 密度:
    0.935±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.6
  • 重原子数:
    24
  • 可旋转键数:
    18
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Role of the hydrophobic moiety of tumor promoters. Synthesis and activity of 2-alkylated benzolactams
    摘要:
    The size and position of a hydrophobic moiety on a benzolactam skeleton, which reproduces the active conformation and biological activity of teleocidins, play an important role in the appearance of the activity. Compounds with alkyl groups of various sizes and shapes at the 2-position of benzolactam were synthesized. Structure-activity results indicate that a hydrophobic substituent at the C-2 position plays a critical role in the appearance of biological activities, as in the case of substitution at C-9. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00580-6
  • 作为产物:
    参考文献:
    名称:
    Role of the hydrophobic moiety of tumor promoters. Synthesis and activity of 2-alkylated benzolactams
    摘要:
    The size and position of a hydrophobic moiety on a benzolactam skeleton, which reproduces the active conformation and biological activity of teleocidins, play an important role in the appearance of the activity. Compounds with alkyl groups of various sizes and shapes at the 2-position of benzolactam were synthesized. Structure-activity results indicate that a hydrophobic substituent at the C-2 position plays a critical role in the appearance of biological activities, as in the case of substitution at C-9. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00580-6
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