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1-[2-[Bis[(2-methylpropan-2-yl)oxy]-oxidophosphaniumyl]oxyethyl]-4-methoxybenzene | 1314357-88-4

中文名称
——
中文别名
——
英文名称
1-[2-[Bis[(2-methylpropan-2-yl)oxy]-oxidophosphaniumyl]oxyethyl]-4-methoxybenzene
英文别名
1-[2-[bis[(2-methylpropan-2-yl)oxy]-oxidophosphaniumyl]oxyethyl]-4-methoxybenzene
1-[2-[Bis[(2-methylpropan-2-yl)oxy]-oxidophosphaniumyl]oxyethyl]-4-methoxybenzene化学式
CAS
1314357-88-4
化学式
C17H29O5P
mdl
——
分子量
344.388
InChiKey
GWQBCZZQFHYMIH-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):
    3.4
  • 重原子数:
    23
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    60
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • 作为产物:
    参考文献:
    名称:
    Phosphonate-free phosphorylation of alcohols using bis-(tert-butyl) phosphoramidite with imidazole·hydrochloride and imidazole as the activator
    摘要:
    A variety of commercially available alcohols were converted to their bis-(tert-butyl) protected monophosphate pro-drugs. The improved procedure uses the unique combination of imidazole center dot hydrochloride and imidazole as the activator to suppress the formation of undesired phosphonate by-product frequently encountered with the bis-(tert-butyl) phosphoramidite reagents. The new activation procedure eliminates the need to use excess reagents. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2011.05.020
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文献信息

  • Phosphonate-free phosphorylation of alcohols using bis-(tert-butyl) phosphoramidite with imidazole·hydrochloride and imidazole as the activator
    作者:Bruno Haché、Lisa Brett、Sagar Shakya
    DOI:10.1016/j.tetlet.2011.05.020
    日期:2011.7
    A variety of commercially available alcohols were converted to their bis-(tert-butyl) protected monophosphate pro-drugs. The improved procedure uses the unique combination of imidazole center dot hydrochloride and imidazole as the activator to suppress the formation of undesired phosphonate by-product frequently encountered with the bis-(tert-butyl) phosphoramidite reagents. The new activation procedure eliminates the need to use excess reagents. (C) 2011 Elsevier Ltd. All rights reserved.
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