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(benzoxy) 3-[1,2-di-(10-undecenyl)-sn-glyceroxy] (N,N-diisopropylamino)phosphine | 188950-57-4

中文名称
——
中文别名
——
英文名称
(benzoxy) 3-[1,2-di-(10-undecenyl)-sn-glyceroxy] (N,N-diisopropylamino)phosphine
英文别名
N-[[(2R)-2,3-bis(undec-10-enoxy)propoxy]-phenylmethoxyphosphanyl]-N-propan-2-ylpropan-2-amine
(benzoxy) 3-[1,2-di-(10-undecenyl)-sn-glyceroxy] (N,N-diisopropylamino)phosphine化学式
CAS
188950-57-4
化学式
C38H68NO4P
mdl
——
分子量
633.936
InChiKey
JJAQFKDMXZYBIF-FBOXOMFYSA-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):
    12.2
  • 重原子数:
    44
  • 可旋转键数:
    32
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.74
  • 拓扑面积:
    40.2
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    (benzoxy) 3-[1,2-di-(10-undecenyl)-sn-glyceroxy] (N,N-diisopropylamino)phosphine四氮唑间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 反应 3.08h, 生成 benzyl 3-[1,2-di-(10-undecenyl)-sn-glyceryl] 1-[2,6-di-O-benzoxymethyl-3-O-benzyl-4,5-O-(p-methoxybenzyl)-D-myo-inosityl] phosphate
    参考文献:
    名称:
    Synthesis of a tritium-labelled diether analog of phosphatidylinositol 4,5-bisphosphate
    摘要:
    The synthesis of 1-(1,2-O-diundecyl-sn-glycerylphosphoryl) 4,5-D-myo-inosityl bisphosphate and its tritiated analog are described. The convergent synthesis employed optically-pure inositol and glycerol derivatives. In the final step, hydrogenation of an alkenyl chain gave the saturated diether PIP2 and tritiation gave the high-specific activity, tritium-labelled analog.
    DOI:
    10.1002/(sici)1099-1344(199703)39:3<251::aid-jlcr964>3.0.co;2-y
  • 作为产物:
    参考文献:
    名称:
    Synthesis of a tritium-labelled diether analog of phosphatidylinositol 4,5-bisphosphate
    摘要:
    The synthesis of 1-(1,2-O-diundecyl-sn-glycerylphosphoryl) 4,5-D-myo-inosityl bisphosphate and its tritiated analog are described. The convergent synthesis employed optically-pure inositol and glycerol derivatives. In the final step, hydrogenation of an alkenyl chain gave the saturated diether PIP2 and tritiation gave the high-specific activity, tritium-labelled analog.
    DOI:
    10.1002/(sici)1099-1344(199703)39:3<251::aid-jlcr964>3.0.co;2-y
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文献信息

  • Synthesis of a tritium-labelled diether analog of phosphatidylinositol 4,5-bisphosphate
    作者:Jian Chen、Glenn D. Prestwich
    DOI:10.1002/(sici)1099-1344(199703)39:3<251::aid-jlcr964>3.0.co;2-y
    日期:1997.3
    The synthesis of 1-(1,2-O-diundecyl-sn-glycerylphosphoryl) 4,5-D-myo-inosityl bisphosphate and its tritiated analog are described. The convergent synthesis employed optically-pure inositol and glycerol derivatives. In the final step, hydrogenation of an alkenyl chain gave the saturated diether PIP2 and tritiation gave the high-specific activity, tritium-labelled analog.
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