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Acetic acid 1-(11-amino-undecyl)-6-oxo-cyclohexa-2,4-dienyl ester | 934972-03-9

中文名称
——
中文别名
——
英文名称
Acetic acid 1-(11-amino-undecyl)-6-oxo-cyclohexa-2,4-dienyl ester
英文别名
[1-(11-Aminoundecyl)-6-oxocyclohexa-2,4-dien-1-yl] acetate
Acetic acid 1-(11-amino-undecyl)-6-oxo-cyclohexa-2,4-dienyl ester化学式
CAS
934972-03-9
化学式
C19H31NO3
mdl
——
分子量
321.46
InChiKey
SBVWVDSXVUUERX-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):
    4.6
  • 重原子数:
    23
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.68
  • 拓扑面积:
    69.4
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    Acetic acid 1-(11-amino-undecyl)-6-oxo-cyclohexa-2,4-dienyl ester四甲基乙二胺 作用下, 以 二氯甲烷 为溶剂, 生成 Acetic acid (4Z,6E)-2-oxo-azacyclooctadeca-4,6-dien-7-yl ester 、 Acetic acid (4Z,6E,22Z,24E)-25-acetoxy-2,20-dioxo-1,19-diaza-cyclohexatriaconta-4,6,22,24-tetraen-7-yl ester
    参考文献:
    名称:
    Photolactamization: A Novel Synthetic Entry into Large Ring-Sized Lactams
    摘要:
    Diene ketenes smoothly accessible by photochemical ring cleavage of omicron-quinol acetates, in the presence of primary or secondary amines afford the corresponding amides. In an intramolecular version of this reaction macrocyclic lactams of type A are produced, if aminoalkylated omicron-quinol acetates of type C are used as photo reactants. These photo reactants are available on acid mediated removal of the Boc-protecting group from Wessely acetoxylation products of type D, easily formed via compounds of type E from aminoalkylated phenols of type F.
    DOI:
    10.1016/0040-4039(92)88118-o
  • 作为产物:
    参考文献:
    名称:
    Photolactamization: A Novel Synthetic Entry into Large Ring-Sized Lactams
    摘要:
    Diene ketenes smoothly accessible by photochemical ring cleavage of omicron-quinol acetates, in the presence of primary or secondary amines afford the corresponding amides. In an intramolecular version of this reaction macrocyclic lactams of type A are produced, if aminoalkylated omicron-quinol acetates of type C are used as photo reactants. These photo reactants are available on acid mediated removal of the Boc-protecting group from Wessely acetoxylation products of type D, easily formed via compounds of type E from aminoalkylated phenols of type F.
    DOI:
    10.1016/0040-4039(92)88118-o
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