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[3-[[Tert-butyl(diphenyl)silyl]oxymethyl]-5-hexadecanoyloxypentyl] hexadecanoate | 649764-96-5

中文名称
——
中文别名
——
英文名称
[3-[[Tert-butyl(diphenyl)silyl]oxymethyl]-5-hexadecanoyloxypentyl] hexadecanoate
英文别名
——
[3-[[Tert-butyl(diphenyl)silyl]oxymethyl]-5-hexadecanoyloxypentyl] hexadecanoate化学式
CAS
649764-96-5
化学式
C54H92O5Si
mdl
——
分子量
849.407
InChiKey
BZALIJATSBQPAX-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:
    790.7±60.0 °C(Predicted)
  • 密度:
    0.97±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    15.01
  • 重原子数:
    60
  • 可旋转键数:
    42
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.74
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:cb8f2a9071a083c4c26e8c91a24c47b2
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反应信息

  • 作为反应物:
    描述:
    [3-[[Tert-butyl(diphenyl)silyl]oxymethyl]-5-hexadecanoyloxypentyl] hexadecanoate四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 16.0h, 以79%的产率得到Hexadecanoic acid 5-hexadecanoyloxy-3-hydroxymethyl-pentyl ester
    参考文献:
    名称:
    Synthesis and Supramolecular Properties of Conformationally Restricted and Flexible Phospholipids
    摘要:
    Short synthetic routes are described to produce structurally related phospholipids that are either conformationally restricted or flexible. The conformationally restricted structures have a cyclopropyl ring in the interfacial region of the phospholipid. The key synthetic step is a cyclopropanation reaction between 2(5H)-furanone and a stabilized chloroallylic phosphonate anion. The synthetic routes enable the incorporation of different polar headgroups as well as nonpolar tails at late stages in the sequence. The phosphoethanolamine derivatives 1b and 2b readily form encapsulating vesicles, however, dye leakage from vesicles composed of the restricted phospholipid 1b is significantly slower than from vesicles composed of flexible analogue 2b. Physicochemical analyses using P-31 NMR, differential scanning calorimetry, fluorescence anisotropy, and Langmuir-Blodgett films suggest that the decreased permeability of membranes composed of conformationally restricted 1b is due to its ability to pack more closely in a bilayer assembly.
    DOI:
    10.1021/jo034843v
  • 作为产物:
    描述:
    4-((tert-butyl-diphenyl-silyloxy)methyl)-1,6-heptadiene 在 氧气臭氧三乙胺 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 1.58h, 生成 [3-[[Tert-butyl(diphenyl)silyl]oxymethyl]-5-hexadecanoyloxypentyl] hexadecanoate
    参考文献:
    名称:
    Synthesis and Supramolecular Properties of Conformationally Restricted and Flexible Phospholipids
    摘要:
    Short synthetic routes are described to produce structurally related phospholipids that are either conformationally restricted or flexible. The conformationally restricted structures have a cyclopropyl ring in the interfacial region of the phospholipid. The key synthetic step is a cyclopropanation reaction between 2(5H)-furanone and a stabilized chloroallylic phosphonate anion. The synthetic routes enable the incorporation of different polar headgroups as well as nonpolar tails at late stages in the sequence. The phosphoethanolamine derivatives 1b and 2b readily form encapsulating vesicles, however, dye leakage from vesicles composed of the restricted phospholipid 1b is significantly slower than from vesicles composed of flexible analogue 2b. Physicochemical analyses using P-31 NMR, differential scanning calorimetry, fluorescence anisotropy, and Langmuir-Blodgett films suggest that the decreased permeability of membranes composed of conformationally restricted 1b is due to its ability to pack more closely in a bilayer assembly.
    DOI:
    10.1021/jo034843v
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文献信息

  • Synthesis and Supramolecular Properties of Conformationally Restricted and Flexible Phospholipids
    作者:Lauri Vares、Atanas V. Koulov、Bradley D. Smith
    DOI:10.1021/jo034843v
    日期:2003.12.1
    Short synthetic routes are described to produce structurally related phospholipids that are either conformationally restricted or flexible. The conformationally restricted structures have a cyclopropyl ring in the interfacial region of the phospholipid. The key synthetic step is a cyclopropanation reaction between 2(5H)-furanone and a stabilized chloroallylic phosphonate anion. The synthetic routes enable the incorporation of different polar headgroups as well as nonpolar tails at late stages in the sequence. The phosphoethanolamine derivatives 1b and 2b readily form encapsulating vesicles, however, dye leakage from vesicles composed of the restricted phospholipid 1b is significantly slower than from vesicles composed of flexible analogue 2b. Physicochemical analyses using P-31 NMR, differential scanning calorimetry, fluorescence anisotropy, and Langmuir-Blodgett films suggest that the decreased permeability of membranes composed of conformationally restricted 1b is due to its ability to pack more closely in a bilayer assembly.
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