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2,6-di-(α-methylbenzyl)-4-methoxyphenol | 16790-04-8

中文名称
——
中文别名
——
英文名称
2,6-di-(α-methylbenzyl)-4-methoxyphenol
英文别名
4-Methoxy-2,6-bis(1-phenylethyl)phenol
2,6-di-(α-methylbenzyl)-4-methoxyphenol化学式
CAS
16790-04-8
化学式
C23H24O2
mdl
——
分子量
332.442
InChiKey
CDDPADFYDLJBIF-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

物化性质

  • 沸点:
    468.0±45.0 °C(Predicted)
  • 密度:
    1.089±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:c7f5186cde669fed5a0529fc19abed64
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反应信息

  • 作为产物:
    描述:
    苯乙烯4-甲氧基苯酚 在 oligomeric (4-methoxyphenoxy)alumoxane 作用下, 以94%的产率得到4-甲氧基-2-(1-苯乙基)-苯酚
    参考文献:
    名称:
    Alkylation of 4-methoxyphenol with styrene in the presence of alumoxane compounds
    摘要:
    The catalytic properties of alumoxane compounds in the alkylation of 4-methoxyphenol with styrene were studied. Structures and yields of alkylation products depend on the amount of catalyst, the phenol: olefin ratio, and the reaction time. Phenoxyalumoxanes are effective ortho-directing catalysts with respect to the hydroxy group. Under optimum conditions, 2-(alpha-methylbenzyl)-4-methoxyphenol and 2,5-di-(alpha-methylbenzyl)-4-methoxyphenol were obtained in 94% and 84-86% yields, respectively.
    DOI:
    10.1007/bf00698972
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文献信息

  • Alkylation of 4-methoxyphenol with styrene in the presence of alumoxane compounds
    作者:F. Kh. Inoyatov、R. Sh. Abubakirov、A. I. Mikaya、I. M. Khrapova、V. M. Perchenko、N. A. Plate
    DOI:10.1007/bf00698972
    日期:1993.5
    The catalytic properties of alumoxane compounds in the alkylation of 4-methoxyphenol with styrene were studied. Structures and yields of alkylation products depend on the amount of catalyst, the phenol: olefin ratio, and the reaction time. Phenoxyalumoxanes are effective ortho-directing catalysts with respect to the hydroxy group. Under optimum conditions, 2-(alpha-methylbenzyl)-4-methoxyphenol and 2,5-di-(alpha-methylbenzyl)-4-methoxyphenol were obtained in 94% and 84-86% yields, respectively.
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