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6-(1-Hydroxy-ethyl)-5,8-dihydro-naphthalene-1,4-diol | 86652-52-0

中文名称
——
中文别名
——
英文名称
6-(1-Hydroxy-ethyl)-5,8-dihydro-naphthalene-1,4-diol
英文别名
6-(1-Hydroxyethyl)-5,8-dihydronaphthalene-1,4-diol
6-(1-Hydroxy-ethyl)-5,8-dihydro-naphthalene-1,4-diol化学式
CAS
86652-52-0
化学式
C12H14O3
mdl
——
分子量
206.241
InChiKey
HZLFNHHTTZSTKL-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):
    1.4
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis in the Field of Natural Products of Biological Relevance
    摘要:
    AbstractThe chemical manipulation of the aminosugar, daunosamine, has resulted in the development of new interesting doxorubicin analogues, namely 4′‐epi‐ and 4′‐deoxydoxorubicin, whereas the total synthesis of new aglycones has provided new structural types of the anthracyclines. In the field of beta‐lactams, efforts aimed to the discovery of original anti‐infective compounds have led to the synthesis of novel “penem” derivatives starting from methyl penicillinate.
    DOI:
    10.1002/bscb.19820911207
  • 作为产物:
    描述:
    2-(α-hydroxyethyl)-1,3-butadiene对苯醌 为溶剂, 以85%的产率得到6-(1-Hydroxy-ethyl)-5,8-dihydro-naphthalene-1,4-diol
    参考文献:
    名称:
    Nero, Stefano Del; Lombardi, Paolo, Gazzetta Chimica Italiana, 1983, vol. 113, # 1/2, p. 125 - 127
    摘要:
    DOI:
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文献信息

  • Synthesis in the Field of Natural Products of Biological Relevance
    作者:Federico Arcamone
    DOI:10.1002/bscb.19820911207
    日期:——
    AbstractThe chemical manipulation of the aminosugar, daunosamine, has resulted in the development of new interesting doxorubicin analogues, namely 4′‐epi‐ and 4′‐deoxydoxorubicin, whereas the total synthesis of new aglycones has provided new structural types of the anthracyclines. In the field of beta‐lactams, efforts aimed to the discovery of original anti‐infective compounds have led to the synthesis of novel “penem” derivatives starting from methyl penicillinate.
  • Nero, Stefano Del; Lombardi, Paolo, Gazzetta Chimica Italiana, 1983, vol. 113, # 1/2, p. 125 - 127
    作者:Nero, Stefano Del、Lombardi, Paolo
    DOI:——
    日期:——
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