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methyl 6-bromo-4-oxo-1,2,3,4-tetrahydronaphthalene-1-carboxylate | 1347754-59-9

中文名称
——
中文别名
——
英文名称
methyl 6-bromo-4-oxo-1,2,3,4-tetrahydronaphthalene-1-carboxylate
英文别名
methyl 6-bromo-4-oxo-2,3-dihydro-1H-naphthalene-1-carboxylate
methyl 6-bromo-4-oxo-1,2,3,4-tetrahydronaphthalene-1-carboxylate化学式
CAS
1347754-59-9
化学式
C12H11BrO3
mdl
——
分子量
283.122
InChiKey
GJDQLHFGSIISHT-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):
    2.3
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    methyl 6-bromo-4-oxo-1,2,3,4-tetrahydronaphthalene-1-carboxylate苯肼溶剂黄146 作用下, 以52%的产率得到methyl 2-bromo-6,11-dihydro-5H-benzo[a]carbazole-5-carboxylate
    参考文献:
    名称:
    Design, synthesis and biological evaluation of substituted 11H-benzo[a]carbazole-5-carboxamides as novel antitumor agents
    摘要:
    A series of novel 11H-benzo[a]carbazole-5-carboxamide derivatives were designed, synthesized and evaluated for their antitumor activity against human cancer A549 and HCT-116 cell lines. Most of the compounds showed potent antitumor activities, and compound 8 displayed remarkable in vitro and in vivo anticancer activity comparable to that of amonafide. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.09.050
  • 作为产物:
    描述:
    甲醇7-bromo-4-hydroxycarbonyltetralone对甲苯磺酸 作用下, 反应 4.0h, 以86%的产率得到methyl 6-bromo-4-oxo-1,2,3,4-tetrahydronaphthalene-1-carboxylate
    参考文献:
    名称:
    Design, synthesis and biological evaluation of substituted 11H-benzo[a]carbazole-5-carboxamides as novel antitumor agents
    摘要:
    A series of novel 11H-benzo[a]carbazole-5-carboxamide derivatives were designed, synthesized and evaluated for their antitumor activity against human cancer A549 and HCT-116 cell lines. Most of the compounds showed potent antitumor activities, and compound 8 displayed remarkable in vitro and in vivo anticancer activity comparable to that of amonafide. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.09.050
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文献信息

  • Design, synthesis and biological evaluation of substituted 11H-benzo[a]carbazole-5-carboxamides as novel antitumor agents
    作者:Yu-Qin Wang、Xiao-Hua Li、Qian He、Yi Chen、Yu-Yuan Xie、Jian Ding、Ze-Hong Miao、Chun-Hao Yang
    DOI:10.1016/j.ejmech.2011.09.050
    日期:2011.12
    A series of novel 11H-benzo[a]carbazole-5-carboxamide derivatives were designed, synthesized and evaluated for their antitumor activity against human cancer A549 and HCT-116 cell lines. Most of the compounds showed potent antitumor activities, and compound 8 displayed remarkable in vitro and in vivo anticancer activity comparable to that of amonafide. (C) 2011 Elsevier Masson SAS. All rights reserved.
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