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7H-Naphtho[1,2-b]carbazole-7,13(12H)-dione | 922192-06-1

中文名称
——
中文别名
——
英文名称
7H-Naphtho[1,2-b]carbazole-7,13(12H)-dione
英文别名
10-azapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(13),3(11),4,6,8,14,16,18,20-nonaene-2,12-dione
7H-Naphtho[1,2-b]carbazole-7,13(12H)-dione化学式
CAS
922192-06-1
化学式
C20H11NO2
mdl
——
分子量
297.313
InChiKey
PSAXRXASUQFPIZ-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:
    591.6±19.0 °C(Predicted)
  • 密度:
    1.445±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    23
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    49.9
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:79a0113ac3d8d09fa7f5d76888d95b66
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反应信息

  • 作为产物:
    描述:
    菲-1,4-二酮 在 palladium diacetate 、 溶剂黄146 作用下, 以 为溶剂, 生成 7H-Naphtho[1,2-b]carbazole-7,13(12H)-dione
    参考文献:
    名称:
    Structure–activity delineation of quinones related to the biologically active Calothrixin B
    摘要:
    Quinones such as Calothrixins A and B display a range of biological properties. As part of our ongoing studies to elucidate the mechanism of action of the Calothrixins, several related quinones were synthesized and tested for biological activity. The results of the structure-activity relationship (SAR) studies are reported here. beta 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.09.090
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文献信息

  • Structure–activity delineation of quinones related to the biologically active Calothrixin B
    作者:Paul H. Bernardo、Christina L.L. Chai、Maurice Le Guen、Geoffrey D. Smith、Paul Waring
    DOI:10.1016/j.bmcl.2006.09.090
    日期:2007.1
    Quinones such as Calothrixins A and B display a range of biological properties. As part of our ongoing studies to elucidate the mechanism of action of the Calothrixins, several related quinones were synthesized and tested for biological activity. The results of the structure-activity relationship (SAR) studies are reported here. beta 2006 Elsevier Ltd. All rights reserved.
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