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tetra[chloro(2-(2-pyrydylmethylamino)-3-(3,5-dimethylpyrazol-1-yl)-propionate)zinc(II)] | 868235-02-3

中文名称
——
中文别名
——
英文名称
tetra[chloro(2-(2-pyrydylmethylamino)-3-(3,5-dimethylpyrazol-1-yl)-propionate)zinc(II)]
英文别名
——
tetra[chloro(2-(2-pyrydylmethylamino)-3-(3,5-dimethylpyrazol-1-yl)-propionate)zinc(II)]化学式
CAS
868235-02-3
化学式
C56H68Cl4N16O8Zn4
mdl
——
分子量
1496.63
InChiKey
ZDNHDOMDLLHYKL-UHFFFAOYSA-F
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    2-(2-pyrydylmethylamino)-3-(3,5-dimethylpyrazol-1-yl)-propionic acid 、 zinc(II) chloride 在 KOH 作用下, 以 甲醇 为溶剂, 以59%的产率得到tetra[chloro(2-(2-pyrydylmethylamino)-3-(3,5-dimethylpyrazol-1-yl)-propionate)zinc(II)]
    参考文献:
    名称:
    Zinc complexes of a new N3O ligand and their biomimetic reactions
    摘要:
    The new N3O ligand 2-(pyridylmethylamino)-3-(3,5-dimethylpyrazol-1-yl)-propionic acid (L1H) was synthesized and converted to L1Zn-Cl and L1Zn-Br. These complexes are tetrameric in the solid state with bridging carboxylate functions. The reaction of deprotonated L1H with zinc nitrate or zinc perchlorate yielded the aqua complexes [L1Zn-OH2] X with X = ClO4- and NO3-, which crystallize as carboxylate-bridged dimers. Their deprotonation produced, in situ, the hydroxide complex L1Zn-OH, which acted as a base toward p-nitrophenol and bis(p-nitrophenyl)phosphoric acid resulting in L1Zn-ONit and L1Zn-OPO(ONit)(2). Tris(p-nitrophenyl)phosphate was cleaved hydrolytically by L1Zn-OH, releasing one p-nitrophenyl group. A kinetic investigation of this cleavage reaction under pseudo-first-order conditions has yielded second-order rate constants k" of 0.9 s(-1) M-1 in 50% aqueous DMSO and 4.0 s(-1) M-1 in 75% aqueous DMSO. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2005.06.071
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