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N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole | 854616-70-9

中文名称
——
中文别名
——
英文名称
N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole
英文别名
——
N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole化学式
CAS
854616-70-9
化学式
C19H23NO3
mdl
——
分子量
313.397
InChiKey
MBXCZJRLIQWUIC-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):
    4.64
  • 重原子数:
    23.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    40.46
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole 在 palladium on activated charcoal 、 sodium methylate对甲苯磺酸三氟乙酸 作用下, 以 四氢呋喃甲醇二氯甲烷 为溶剂, 反应 47.67h, 生成 5-[4-(1-butylpentyloxy)-2,6-dimethylphenyl]-1,9-bis[3-(hydroxymethyl)phenyl]-10H-dipyrrin
    参考文献:
    名称:
    Highly Sodium-Selective Fluoroionophore Based on Conformational Restriction of Oligoethyleneglycol-Bridged Biaryl Boron−Dipyrromethene
    摘要:
    A non-PET and non-PCT fluoroionophore has been designed and synthesized based on the combination of a biaryl boron-dipyrromethene fluorophore with an oligoethyleneglycol bridge. A specific red-shift response of absorption for NaClO4 in acetonitrile was demonstrated based on conformational restriction triggered by cation recognition at the bridge. The concentration of Na+ can be determined accurately using fluorescence due to a high extinction coefficient (epsilon = 50 000), a high fluorescence quantum yield (Phif = 0.68), and the sharpness of absorption and emission peaks of the boron-dipyrromethene derivative.
    DOI:
    10.1021/ja042414o
  • 作为产物:
    描述:
    3-溴苯甲醇四(三苯基膦)钯正丁基锂 、 sodium hydride 、 sodium carbonate 作用下, 以 四氢呋喃甲醇正己烷甲苯 为溶剂, 反应 39.0h, 生成 N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole
    参考文献:
    名称:
    Highly Sodium-Selective Fluoroionophore Based on Conformational Restriction of Oligoethyleneglycol-Bridged Biaryl Boron−Dipyrromethene
    摘要:
    A non-PET and non-PCT fluoroionophore has been designed and synthesized based on the combination of a biaryl boron-dipyrromethene fluorophore with an oligoethyleneglycol bridge. A specific red-shift response of absorption for NaClO4 in acetonitrile was demonstrated based on conformational restriction triggered by cation recognition at the bridge. The concentration of Na+ can be determined accurately using fluorescence due to a high extinction coefficient (epsilon = 50 000), a high fluorescence quantum yield (Phif = 0.68), and the sharpness of absorption and emission peaks of the boron-dipyrromethene derivative.
    DOI:
    10.1021/ja042414o
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