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N-9-phenanthrylmethylacrylamide | 1422468-50-5

中文名称
——
中文别名
——
英文名称
N-9-phenanthrylmethylacrylamide
英文别名
N-(phenanthren-9-ylmethyl)prop-2-enamide
N-9-phenanthrylmethylacrylamide化学式
CAS
1422468-50-5
化学式
C18H15NO
mdl
——
分子量
261.323
InChiKey
BLTHMUGXXKPJIY-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:
    538.6±33.0 °C(Predicted)
  • 密度:
    1.163±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

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:
    9-甲醛菲 在 sodium tetrahydroborate 、 sodium azide 、 四溴化碳三乙胺三苯基膦 作用下, 以 四氢呋喃 为溶剂, 生成 N-9-phenanthrylmethylacrylamide
    参考文献:
    名称:
    Macroscopic Self-Assembly Based on Molecular Recognition: Effect of Linkage between Aromatics and the Polyacrylamide Gel Scaffold, Amide versus Ester
    摘要:
    The interactions of polyacrylamide- (pAAm-) based gels possessing cyclodextrin (CD) residues (CD-gels) with pAAm-based gels modified with aromatic residues through amide and ester linkages (ArA-gels and ME-gels, respectively) were investigated to examine the effect of linkage (i.e., amide and ester) between aromatic residues and the pAAm gel scaffold. In the present study, benzyl (Bz), 2-naphthylmethyl (Np), 9-phenanthrylmethyl (Ph), and 1-pyrenylmethyl (Py) residues were chosen as a series of aromatic residues. alpha CD-gel did not interact notably with the MA-gels and ME-gels in water. beta CD-gel interacted with the MA-gels and ME-gels possessing smaller aromatic residues (i.e., Bz and Np residues) in water to form gel assemblies. gamma CD-gel showed different tendencies of its interactions with the MA-gels and with the ME-gels; gamma CD-gel interacted with the MA-gels carrying larger aromatic residues (i.e., Ph and Py residues), while gamma CD-gel formed stable gel assemblies only with NpE-gel among the ME-gels examined. This is because gamma CD residues in gamma CD-gel included favorably dimeric aromatic residues in the MA-gels and ME-gels. Reflection fluorescence spectra for the MA-gels and ME-gels possessing fluorescent aromatic residues (i.e., Np, Ph, and Py residues) in the presence of 10 mM gamma CD were indicative of weak selectivities of gamma CD toward NpE, PhA, and PyA residues. Such weak selectivities may be largely enhanced in the macroscopic observation of interaction of CD-gels with the ArA-gels and ME-gels presumably because of multivalency.
    DOI:
    10.1021/ma302344x
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