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| 1253857-49-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1253857-49-6
化学式
C47H60N8NiO5
mdl
——
分子量
875.734
InChiKey
HJEFLLMXKNRLGX-WOXBQKIXSA-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

反应信息

  • 作为产物:
    描述:
    nickel(II) acetate tetrahydrate 作用下, 以 N,N-二甲基甲酰胺氯苯 为溶剂, 反应 14.0h, 以87%的产率得到
    参考文献:
    名称:
    The synthesis and characterisation of carbohydrate-functionalised porphyrazines
    摘要:
    A synthetic pathway to the incorporation of mono- and disaccharide carbohydrate moieties into porphyrazine systems was demonstrated. A range of selectively protected monosaccharide precursors was coupled to a small variety of phthalonitriles, the intermediates were co-macrocyclised to form hybrid porphyrazines in Linstead macrocyclisation reactions Demetallisation of Mg-porphyrazine products was readily effected to afford the free-base pigments, which were subsequently converted into their zinc or nickel complexes Some porphyrazines were deprotected of their isopropylidene groups (on the carbohydrate moieties) under acidic conditions to reveal polar OH groups The extraction coefficients of the porphyrazines between 2-octanol and phosphate buffered saline solution were measured. Comparison of the partition coefficients of the carbohydrate-substituted porphyrazines and their deprotected counterparts revealed that structural alteration offers a way to significantly increase the hydrophilicity of substituted porphyrazines (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2010.05.002
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