摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

bis(p-tert-butoxyphenyl) disulfide | 60852-03-1

中文名称
——
中文别名
——
英文名称
bis(p-tert-butoxyphenyl) disulfide
英文别名
Bis-<4-t-butoxyphenyl>-disulfid;1,1'-Disulfanediylbis(4-tert-butoxybenzene);1-[(2-methylpropan-2-yl)oxy]-4-[[4-[(2-methylpropan-2-yl)oxy]phenyl]disulfanyl]benzene
bis(p-tert-butoxyphenyl) disulfide化学式
CAS
60852-03-1
化学式
C20H26O2S2
mdl
——
分子量
362.557
InChiKey
SWKSMVZQRRCVQY-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):
    5.9
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    69.1
  • 氢给体数:
    0
  • 氢受体数:
    4

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
  • 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:
    bis(p-tert-butoxyphenyl) disulfide 生成 (E)-4-(2-Chlordiphenylvinylthio)-phenol
    参考文献:
    名称:
    4-t-Butoxybenzenesulfenyl Chloride. Synthesis and Characterization
    摘要:
    DOI:
    10.1055/s-1976-24075
  • 作为产物:
    参考文献:
    名称:
    4-t-Butoxybenzenesulfenyl Chloride. Synthesis and Characterization
    摘要:
    DOI:
    10.1055/s-1976-24075
点击查看最新优质反应信息

文献信息

  • Magnetic Field Effects Observed upon Photolysis of Para-Substituted Diphenyl Disulfides in Micellar Solutions
    作者:Gunnar Jeschke、Masanobu Wakasa、Yoshio Sakaguchi、Hisaharu Hayashi
    DOI:10.1021/j100066a027
    日期:1994.4
    The recombination of pairs of para-substituted phenylthiyl radicals inside micellar supercages was studied by means of a nanosecond laser flash photolysis technique. Singlet and triplet pairs were formed by direct excitation and by triplet-sensitized photolysis of the corresponding disulfides, respectively. Magnetic field effects (MFEs) on the yield of escaped thiyl radicals were found for the triplet-sensitized photolysis of the p-amino compound. For the p-hydroxy-, p-methoxy-, and p-butoxy compounds, short-lived MFEs were observed but it is unlikely that they arise from the recombination of the thiyl radicals. No MFE was found on pairs of p-chloro-substituted and unsubstituted phenylthiyl radicals within experimental error. The absence of MFE is in this case explained by large spin-orbit coupling caused by orbital degeneracy. A stabilization mechanism of the (p-aminophenyl)-thiyl radicals lifts that degeneracy and reduces spin-orbit coupling. Variations of the MFE over the absorption spectrum were used to assign the MFEs to certain species in the reaction systems.
  • 4-<i>t</i>-Butoxybenzenesulfenyl Chloride. Synthesis and Characterization
    作者:Franco MARCUZZI、Giovanni MELLONI
    DOI:10.1055/s-1976-24075
    日期:——
查看更多