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(4Z)-2,3,8-trimethyldipyrrin-1(10H)-one | 868829-16-7

中文名称
——
中文别名
——
英文名称
(4Z)-2,3,8-trimethyldipyrrin-1(10H)-one
英文别名
——
(4Z)-2,3,8-trimethyldipyrrin-1(10H)-one化学式
CAS
868829-16-7
化学式
C12H14N2O
mdl
——
分子量
202.256
InChiKey
WKNZPCUHYRTNFU-WZUFQYTHSA-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):
    2.13
  • 重原子数:
    15.0
  • 可旋转键数:
    1.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    44.89
  • 氢给体数:
    2.0
  • 氢受体数:
    1.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (4Z)-2,3,8-trimethyldipyrrin-1(10H)-one三氟乙酸 作用下, 反应 4.1h, 生成 (4Z,9Z,15Z)-2,3,8,12,17,18-hexamethylbilin-1,19-(21H,24H)-dione
    参考文献:
    名称:
    Inducing anti-Conformers of Biliverdin Chromophores by Reducing Sterical Hindrance
    摘要:
    Two different types of conformational changes of the biliverdin chromophore were accomplished by the concept of reducing sterical hindrance. On one hand, model compounds unsubstituted at position 7 and/or 13 adopt the semi-extended geometry with anti-conformation of the dipyrrinone moiety. On the other hand, stretching of the chromophore with anti-conformation of the dipyrrin substructure was achieved with a model compound unsubstituted at position 12. Both kinds of anti-conformations have been proved by 2D NMR and UV-Vis spectroscopy.
    DOI:
    10.1007/s00706-004-0268-5
  • 作为产物:
    描述:
    (4Z)-9-carboxy-2,3,8-trimethyldipyrrin-1(10H)-one三氟乙酸 作用下, 反应 1.0h, 以85%的产率得到(4Z)-2,3,8-trimethyldipyrrin-1(10H)-one
    参考文献:
    名称:
    Inducing anti-Conformers of Biliverdin Chromophores by Reducing Sterical Hindrance
    摘要:
    Two different types of conformational changes of the biliverdin chromophore were accomplished by the concept of reducing sterical hindrance. On one hand, model compounds unsubstituted at position 7 and/or 13 adopt the semi-extended geometry with anti-conformation of the dipyrrinone moiety. On the other hand, stretching of the chromophore with anti-conformation of the dipyrrin substructure was achieved with a model compound unsubstituted at position 12. Both kinds of anti-conformations have been proved by 2D NMR and UV-Vis spectroscopy.
    DOI:
    10.1007/s00706-004-0268-5
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