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Dodecanoic acid 2-acetylphenyl ester | 158634-27-6

中文名称
——
中文别名
——
英文名称
Dodecanoic acid 2-acetylphenyl ester
英文别名
(2-Acetylphenyl) dodecanoate
Dodecanoic acid 2-acetylphenyl ester化学式
CAS
158634-27-6
化学式
C20H30O3
mdl
——
分子量
318.456
InChiKey
CKFLNSXABQWZCQ-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):
    6.1
  • 重原子数:
    23
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    Dodecanoic acid 2-acetylphenyl ester氢氧化钾硫酸 作用下, 以 吡啶溶剂黄146 为溶剂, 反应 3.0h, 生成 2-Undecylchromen-4-one
    参考文献:
    名称:
    Synthesis and Properties of a New Family of Chiral Mesogens Containing the 2,3-Dihydrobenzopyran Nucleus
    摘要:
    A new class of mesogens A with a central chiral core based on the 2,3-dihydrobenzopyran nucleus was synthesized both in the racemic and optically pure form, and the thermotropic properties were studied. The distortion from structural linearity due to the presence of the 2,3-dihydropyran ring does not inhibit the existence of mesophases, and Ch, S-A, and S-C phases were observed according to the substituents present. The conformational constrictions imposed by cyclization proved not to be very important in determining the compactness of the cholesteric helix.
    DOI:
    10.1021/jo00099a022
  • 作为产物:
    描述:
    月桂酰氯2'-羟基苯乙酮吡啶 作用下, 反应 1.0h, 以91%的产率得到Dodecanoic acid 2-acetylphenyl ester
    参考文献:
    名称:
    Synthesis and Properties of a New Family of Chiral Mesogens Containing the 2,3-Dihydrobenzopyran Nucleus
    摘要:
    A new class of mesogens A with a central chiral core based on the 2,3-dihydrobenzopyran nucleus was synthesized both in the racemic and optically pure form, and the thermotropic properties were studied. The distortion from structural linearity due to the presence of the 2,3-dihydropyran ring does not inhibit the existence of mesophases, and Ch, S-A, and S-C phases were observed according to the substituents present. The conformational constrictions imposed by cyclization proved not to be very important in determining the compactness of the cholesteric helix.
    DOI:
    10.1021/jo00099a022
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文献信息

  • Synthesis and Properties of a New Family of Chiral Mesogens Containing the 2,3-Dihydrobenzopyran Nucleus
    作者:Bianca F. Bonini、Paolo Carboni、Giovanni Gottarelli、Stefano Masiero、Gian Piero Spada
    DOI:10.1021/jo00099a022
    日期:1994.10
    A new class of mesogens A with a central chiral core based on the 2,3-dihydrobenzopyran nucleus was synthesized both in the racemic and optically pure form, and the thermotropic properties were studied. The distortion from structural linearity due to the presence of the 2,3-dihydropyran ring does not inhibit the existence of mesophases, and Ch, S-A, and S-C phases were observed according to the substituents present. The conformational constrictions imposed by cyclization proved not to be very important in determining the compactness of the cholesteric helix.
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