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3-[(Z)-2-benzylsulfanylethenyl]-5-(4-methoxyphenyl)-2,5-dihydrofuran-2-ol | 220338-01-2

中文名称
——
中文别名
——
英文名称
3-[(Z)-2-benzylsulfanylethenyl]-5-(4-methoxyphenyl)-2,5-dihydrofuran-2-ol
英文别名
——
3-[(Z)-2-benzylsulfanylethenyl]-5-(4-methoxyphenyl)-2,5-dihydrofuran-2-ol化学式
CAS
220338-01-2
化学式
C20H20O3S
mdl
——
分子量
340.443
InChiKey
WVFAMFUWJBDTIF-QXMHVHEDSA-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):
    3.4
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    64
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

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文献信息

  • Coupling Reactions and Coupling−Alkylations of Thiophenecarbaldehydes Promoted by Samarium Diiodide
    作者:Shyh-Ming Yang、Jim-Min Fang
    DOI:10.1021/jo980851d
    日期:1999.1.1
    The coupling reactions of 2-thiophenecarbaldehyde with aromatic or aliphatic aldehydes were promoted by samarium diiodide in the presence of hexamethylphosphoramide to give C-5 hydroxyalkylation products. The coupling reactions of 3-thiophenecarbaldehyde occurred at C-2, and the subsequent alkylations occurred at the sulfur atom, accompanied by a concurrent opening of the thiophene ring to afford gamma-lactols. Double hydroxyalkylations of 2- and 3-thiophenecarbaldehydes were also carried out under appropriate reaction conditions. Synthetic applications of these thiophenecarbonyl coupling products were demonstrated, for example, by elaboration to furans, butenolides, and thiophene-fused polycyclic compounds.
  • Yang, Shyn-Ming; Fang, Jim-Min, Journal of the Chemical Society. Perkin transactions I, 1995, # 21, p. 2669 - 2672
    作者:Yang, Shyn-Ming、Fang, Jim-Min
    DOI:——
    日期:——
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