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2,6-Di-t-butyl-4-[(4-chlorophenyldimethylsilyl)methyloxy]phenol

中文名称
——
中文别名
——
英文名称
2,6-Di-t-butyl-4-[(4-chlorophenyldimethylsilyl)methyloxy]phenol
英文别名
2,6 Di-t-butyl-4[(4-chlorophenyldimethylsilyl)methyloxy]phenol;2,6-Ditert-butyl-4-[[(4-chlorophenyl)-dimethylsilyl]methoxy]phenol
2,6-Di-t-butyl-4-[(4-chlorophenyldimethylsilyl)methyloxy]phenol化学式
CAS
——
化学式
C23H33ClO2Si
mdl
——
分子量
405.052
InChiKey
NDIRWEDIPADZPK-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):
    6.17
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为产物:
    描述:
    2,6-二叔丁基苯醌 在 sodium tetrahydroborate 、 potassium carbonate 作用下, 以 乙腈 为溶剂, 生成 2,6-Di-t-butyl-4-[(4-chlorophenyldimethylsilyl)methyloxy]phenol
    参考文献:
    名称:
    Antioxidant and cholesterol lowering properties of 2,6-DI-t-butyl-4-[(dimethylphenylsilyl)methyloxy]phenol and derivatives: A new class of anti-atherogenic compounds
    摘要:
    Di-t-butylphenol derivatives were synthesized and evaluated as antioxidants and cholesterol lowering agents. When evaluated in cholesterol-fed rabbits, the compounds were found to exhibit both properties. Of special interest was the finding that several of the compounds elevated HDL cholesterol levels. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/s0960-894x(96)00273-9
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文献信息

  • Antioxidant and cholesterol lowering properties of 2,6-DI-t-butyl-4-[(dimethylphenylsilyl)methyloxy]phenol and derivatives: A new class of anti-atherogenic compounds
    作者:Roger A. Parker、Roger L. Barnhart、Kim S. Chen、Michael L. Edwards、James E. Matt、Barry L. Rhinehart、Keith M. Robinson、Mark J. Vaal、Mark T. Yates
    DOI:10.1016/s0960-894x(96)00273-9
    日期:1996.7
    Di-t-butylphenol derivatives were synthesized and evaluated as antioxidants and cholesterol lowering agents. When evaluated in cholesterol-fed rabbits, the compounds were found to exhibit both properties. Of special interest was the finding that several of the compounds elevated HDL cholesterol levels. Copyright (C) 1996 Elsevier Science Ltd
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