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γ-tocopherol

中文名称
——
中文别名
——
英文名称
γ-tocopherol
英文别名
2-Hexadecyl-2,7,8-trimethyl-3,4-dihydrochromen-6-ol;2-hexadecyl-2,7,8-trimethyl-3,4-dihydrochromen-6-ol
γ-tocopherol化学式
CAS
——
化学式
C28H48O2
mdl
——
分子量
416.688
InChiKey
DKMAKBZATFEKBF-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):
    11.2
  • 重原子数:
    30
  • 可旋转键数:
    15
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 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:
    γ-tocopherol1,1,3,3-四甲氧基丙烷三氟乙酸 作用下, 反应 2.0h, 以35%的产率得到6,9,10,16,17,20-hexamethyl-6,20-di(4,8,12-trimethyltridecyl)-7,12,14,19-tetraoxahexacyclo[11.11.1.02,11.03,8.015,24.018,23]pentacosa-2,8,10,15(24),16,18(23)-hexaene
    参考文献:
    名称:
    Novel tocopheryl compounds XX. 1,3,8-Trioxaphenanthrenes derived from γ-tocopherol
    摘要:
    Condensation of gamma-tocopherol with aldehydes provides 2,4-disubstituted 1,3,8-trioxaphenanthrenes in a simple one-pot reaction. The reaction proceeded under acid catalysis according to a two-step alkylation-acetalisation mechanism in yields between 58 and 81 %. The title compounds are precursors for the thermal generation of ortho-quinone methides, which can be in situ reduced to give antioxidants of the 5a-substituted alpha-tocopherol-type. The products were analytically characterized by NMR and HRMS. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.07.038
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文献信息

  • Novel tocopheryl compounds XX. 1,3,8-Trioxaphenanthrenes derived from γ-tocopherol
    作者:Christian Adelwöhrer、Thomas Rosenau
    DOI:10.1016/j.tet.2005.07.038
    日期:2005.9
    Condensation of gamma-tocopherol with aldehydes provides 2,4-disubstituted 1,3,8-trioxaphenanthrenes in a simple one-pot reaction. The reaction proceeded under acid catalysis according to a two-step alkylation-acetalisation mechanism in yields between 58 and 81 %. The title compounds are precursors for the thermal generation of ortho-quinone methides, which can be in situ reduced to give antioxidants of the 5a-substituted alpha-tocopherol-type. The products were analytically characterized by NMR and HRMS. (c) 2005 Elsevier Ltd. All rights reserved.
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