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3-(2,4,6-trichloronaphthalen-1-yl)propanal | 108579-11-9

中文名称
——
中文别名
——
英文名称
3-(2,4,6-trichloronaphthalen-1-yl)propanal
英文别名
——
3-(2,4,6-trichloronaphthalen-1-yl)propanal化学式
CAS
108579-11-9
化学式
C13H9Cl3O
mdl
——
分子量
287.573
InChiKey
RUZQSZHBDKVQAZ-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):
    4.7
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    4,6-dichloro-7-iodoindan-1-ol 生成 3-(2,4,6-trichloronaphthalen-1-yl)propanal
    参考文献:
    名称:
    3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 6. trans-6-[2-(Substituted-1-naphthyl)ethyl(or ethenyl)]-3,4,5,6-tetrahydro-4-hydroxy-2H-pyran-2-ones
    摘要:
    A variety of trans-6-[2-(substituted-1-naphthyl)ethyl(or ethenyl)]-3,4,5,6-tetrahydro-4-hydroxy-2H-pyran-2-ones were prepared and, upon conversion to their 3,5-dihydroxy carboxylates, were found to have good inhibitory activity against the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-determining enzyme in cholesterogenesis. The most active compounds are 2,4,6- and 2,4,7-trichloro derivatives and would be expected to display about the same potency as the standard compactin upon resolution.
    DOI:
    10.1021/jm00164a047
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文献信息

  • US4654363A
    申请人:——
    公开号:US4654363A
    公开(公告)日:1987-03-31
  • 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 6. trans-6-[2-(Substituted-1-naphthyl)ethyl(or ethenyl)]-3,4,5,6-tetrahydro-4-hydroxy-2H-pyran-2-ones
    作者:John D. Prugh、Alfred W. Alberts、Albert A. Deana、James L. Gilfillian、Jesse W. Huff、Robert L. Smith、J. Mark Wiggins
    DOI:10.1021/jm00164a047
    日期:1990.2
    A variety of trans-6-[2-(substituted-1-naphthyl)ethyl(or ethenyl)]-3,4,5,6-tetrahydro-4-hydroxy-2H-pyran-2-ones were prepared and, upon conversion to their 3,5-dihydroxy carboxylates, were found to have good inhibitory activity against the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-determining enzyme in cholesterogenesis. The most active compounds are 2,4,6- and 2,4,7-trichloro derivatives and would be expected to display about the same potency as the standard compactin upon resolution.
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