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3,5-bis(3,5-bis[3-(tert-butyldimethylsilyloxy)propyloxy]benzyloxy)benzyl alcohol | 247123-01-9

中文名称
——
中文别名
——
英文名称
3,5-bis(3,5-bis[3-(tert-butyldimethylsilyloxy)propyloxy]benzyloxy)benzyl alcohol
英文别名
[3,5-Bis[[3,5-bis[3-[tert-butyl(dimethyl)silyl]oxypropoxy]phenyl]methoxy]phenyl]methanol;[3,5-bis[[3,5-bis[3-[tert-butyl(dimethyl)silyl]oxypropoxy]phenyl]methoxy]phenyl]methanol
3,5-bis(3,5-bis[3-(tert-butyldimethylsilyloxy)propyloxy]benzyloxy)benzyl alcohol化学式
CAS
247123-01-9
化学式
C57H100O11Si4
mdl
——
分子量
1073.76
InChiKey
MRKMHXAIMGKOIH-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):
    15.5
  • 重原子数:
    72
  • 可旋转键数:
    35
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.68
  • 拓扑面积:
    113
  • 氢给体数:
    1
  • 氢受体数:
    11

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

  • 作为反应物:
    描述:
    甲基磺酰氯3,5-bis(3,5-bis[3-(tert-butyldimethylsilyloxy)propyloxy]benzyloxy)benzyl alcohol三乙胺 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 2.5h, 生成 Methanesulfonic acid 3,5-bis-{3,5-bis-[3-(tert-butyl-dimethyl-silanyloxy)-propoxy]-benzyloxy}-benzyl ester
    参考文献:
    名称:
    Dendrimeric Organochalcogen Catalysts for the Activation of Hydrogen Peroxide:  Improved Catalytic Activity through Statistical Effects and Cooperativity in Successive Generations
    摘要:
    Dendrimeric polyphenylsulfides, -selenides, and -tellurides are prepared in high yield using propyloxy spacers to connect the phenylchalcogeno groups to the dendrimeric core. The selenides and tellurides catalyze the oxidation of bromide with hydrogen peroxide to give positive bromine species that can be captured by cyclohexene in two-phase systems. The corresponding sulfides show no catalytic activity. The increase in the rate of catalysis followed statistical effects for 1, 6, and 12 phenyltelluro groups. However, the increase in the rate of catalysis exceeds statistical contributions for the first few generations with 1, 3, 6, and 12 phenylseleno groups and suggested cooperativity among phenylseleno groups. The increase in catalytic rate was lost upon replacing all but one phenylseleno group with phenoxy groups. On the basis of H2O2 consumed, the dendrimer with 12 phenylseleno groups has a turnover number of >60 000 mol of H2O2 consumed per mole of catalyst.
    DOI:
    10.1021/ja002649+
  • 作为产物:
    参考文献:
    名称:
    Dendrimeric Catalysts for the Activation of Hydrogen Peroxide. Increasing Activity per Catalytic Phenylseleno Group in Successive Generations
    摘要:
    [GRAPHICS]Dendrimeric polyphenylselenides are prepared in high yield using propyloxy spacers to connect the phenyseleno groups to the dendrimeric core. The selenides catalyze the oxidation of bromide with hydrogen peroxide to give positive bromine species that can be captured by cyclohexene in two-phase systems. The increase in the rate of catalysis exceeds statistical contributions for the first few generations with 3, 6, and 12 phenylseleno groups.
    DOI:
    10.1021/ol990836a
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文献信息

  • Dendrimeric Organochalcogen Catalysts for the Activation of Hydrogen Peroxide:  Improved Catalytic Activity through Statistical Effects and Cooperativity in Successive Generations
    作者:Charles Francavilla、Michael D. Drake、Frank V. Bright、Michael R. Detty
    DOI:10.1021/ja002649+
    日期:2001.1.1
    Dendrimeric polyphenylsulfides, -selenides, and -tellurides are prepared in high yield using propyloxy spacers to connect the phenylchalcogeno groups to the dendrimeric core. The selenides and tellurides catalyze the oxidation of bromide with hydrogen peroxide to give positive bromine species that can be captured by cyclohexene in two-phase systems. The corresponding sulfides show no catalytic activity. The increase in the rate of catalysis followed statistical effects for 1, 6, and 12 phenyltelluro groups. However, the increase in the rate of catalysis exceeds statistical contributions for the first few generations with 1, 3, 6, and 12 phenylseleno groups and suggested cooperativity among phenylseleno groups. The increase in catalytic rate was lost upon replacing all but one phenylseleno group with phenoxy groups. On the basis of H2O2 consumed, the dendrimer with 12 phenylseleno groups has a turnover number of >60 000 mol of H2O2 consumed per mole of catalyst.
  • Dendrimeric Catalysts for the Activation of Hydrogen Peroxide. Increasing Activity per Catalytic Phenylseleno Group in Successive Generations
    作者:Charles Francavilla、Frank V. Bright、Michael R. Detty
    DOI:10.1021/ol990836a
    日期:1999.10.1
    [GRAPHICS]Dendrimeric polyphenylselenides are prepared in high yield using propyloxy spacers to connect the phenyseleno groups to the dendrimeric core. The selenides catalyze the oxidation of bromide with hydrogen peroxide to give positive bromine species that can be captured by cyclohexene in two-phase systems. The increase in the rate of catalysis exceeds statistical contributions for the first few generations with 3, 6, and 12 phenylseleno groups.
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