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2-naphthoxy-triethylene glycol methacrylate | 1305339-09-6

中文名称
——
中文别名
——
英文名称
2-naphthoxy-triethylene glycol methacrylate
英文别名
2-[2-(2-Naphthalen-2-yloxyethoxy)ethoxy]ethyl 2-methylprop-2-enoate;2-[2-(2-naphthalen-2-yloxyethoxy)ethoxy]ethyl 2-methylprop-2-enoate
2-naphthoxy-triethylene glycol methacrylate化学式
CAS
1305339-09-6
化学式
C20H24O5
mdl
——
分子量
344.408
InChiKey
QSIQLVWTOWUKBP-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):
    3.7
  • 重原子数:
    25
  • 可旋转键数:
    12
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    54
  • 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:
    描述:
    2-(2-(2-(naphthalen-2-yloxy)ethoxy)ethoxy)ethanol甲基丙烯酰氯三乙胺 作用下, 以 乙醚 为溶剂, 以85%的产率得到2-naphthoxy-triethylene glycol methacrylate
    参考文献:
    名称:
    Supramolecular Glycopolymers in Water: A Reversible Route Toward Multivalent Carbohydrate–Lectin Conjugates Using Cucurbit[8]uril
    摘要:
    Supramolecular self-assembly and reversible switching has been demonstrated for the first time between monovalent and multivalent carbohydrate ligands and the multivalency effect on lectin binding has been investigated. The self-assembly process is mediated through noncovalent interactions between pendant moieties on a polymer scaffold and a monosaccharide-functionalized viologen with cucurbit-[8]uril (CB[8]) acting as a "supramolecular handcuff". The rate of binding of the tetrameric lectin Concanavalin A (Con A) to a mannose-containing supramolecular glycopolymer was investigated through a standard turbidimetric assay.
    DOI:
    10.1021/ma200343q
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文献信息

  • Supramolecular Glycopolymers in Water: A Reversible Route Toward Multivalent Carbohydrate–Lectin Conjugates Using Cucurbit[8]uril
    作者:Jin Geng、Frank Biedermann、Jameel M. Zayed、Feng Tian、Oren A. Scherman
    DOI:10.1021/ma200343q
    日期:2011.6.14
    Supramolecular self-assembly and reversible switching has been demonstrated for the first time between monovalent and multivalent carbohydrate ligands and the multivalency effect on lectin binding has been investigated. The self-assembly process is mediated through noncovalent interactions between pendant moieties on a polymer scaffold and a monosaccharide-functionalized viologen with cucurbit-[8]uril (CB[8]) acting as a "supramolecular handcuff". The rate of binding of the tetrameric lectin Concanavalin A (Con A) to a mannose-containing supramolecular glycopolymer was investigated through a standard turbidimetric assay.
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