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1,4-bis((4-iodo-3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene | 1412315-34-4

中文名称
——
中文别名
——
英文名称
1,4-bis((4-iodo-3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene
英文别名
4-Iodo-1-[[4-[(4-iodo-3,5-dimethylpyrazol-1-yl)methyl]phenyl]methyl]-3,5-dimethylpyrazole
1,4-bis((4-iodo-3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene化学式
CAS
1412315-34-4
化学式
C18H20I2N4
mdl
——
分子量
546.193
InChiKey
LGDLCAWRJJUNMX-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):
    4.6
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    35.6
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    对二甲苯 、 potassium hydroxide 作用下, 以 二甲基亚砜 为溶剂, 反应 6.0h, 生成 1,4-bis((4-iodo-3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene
    参考文献:
    名称:
    Synthesis, structural, and biological evaluation of the arene-linked pyrazolyl methane ligands and their d9/d10 metal complexes
    摘要:
    A series of the p-bis[(1-pyrazolyl)methyl] benzene ligands (L-1-L-6) in the DMSO system were synthesized. In the mean time, by using the ligands as a linker, a new family of transition metal coordination polymers, namely, [Cu-2(L-1)(2)Cl-4] (1), [Cu-2(L-2)(2)Cl-4] (2), [Ag(L-2)(NO3)] (3). [Zn-2(L-2)(2)(SCN)(4)] (4) and [Cd-2(L-2)(SCN)(4)] (5) [L-1 = 1,4-bis((1H-pyrazol-1-yl)methyl)benzene; L-2 = 1,4-bis(3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene] have been constructed by the reaction of the p-bis[(1-pyrazolyl)methyl]benzene and corresponding to the transition metal compounds in a mixed solution of CH3OH/C2H5OH at mild temperature condition. All the coordination polymers and p-bis[(1-pyrazolyl)methyl]benzene ligands were characterized by elemental analysis, IR spectroscopy, H-1 NMR and C-13 NMR, and some of them were characterized by UV spectroscopy, thermogravimetric analysis, X-ray powder and X-ray single-crystal diffraction. Structural analyses reveal that the ligands L-3-L-5 (L-3 = 1,4-bis((4-iodo-1H-pyrazol-1-yl)methyl)benzene, L-4 = 1,4-bis((4-iodo-3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene, L-5 = 1,4-bis((4-nitro-1H-pyrazol-1-yl)methyl) benzene,L-6 = 1,4-bis((4-nitro-3,5-dimethyl-1H-pyrazol-1-yl) methyl) benzene) are discrete organic compound molecules and the complexes 1-5 are 1D M-L-M coordination polymers, which are further interlinked via hydrogen bonds resulting in 2D or even 3D supermolecular networks. The luminescent properties of the coordination polymers 3,4 and 5 were examined by luminescence spectra. The analytic results indicate that different metal complexes with the same ligand have different influence on the characteristic photoluminescence. Furthermore, the cytotoxicity of the ligands L-1-L-6 and complexes 1-5 were evaluated against hepG2 cells. For the ligands of L-1-L-6, the different substituents of the pyrazole ring slightly influenced the cytotoxicity of the cell. It is found that nitro-compounds have shown the highest cytotoxicity under the same concentration condition. The cytotoxic activity of the complexes 1-5 are strongly increased by the introduction of the transition metals. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2012.08.016
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文献信息

  • Molecular design and the optimum synthetic route of the compounds with multi-pyrazole and its derivatives and the potential application in antibacterial agents
    作者:Ji-Xiao Wang、Zi-Ran Zhu、Feng-Ying Bai、Xin-Yu Wang、Xiao-Xi Zhang、Yong-Heng Xing
    DOI:10.1016/j.poly.2015.06.020
    日期:2015.10
    Molecular design and efficient synthetic procedures have been developed for pyrazole and its derivatives with different linkers. In particular, twelve compounds with -I or -NO2 substituted groups on the pyrazole ring were synthesized for the first time. These compounds are characterized by element analysis, IR, HNMR, M.P. and X-ray diffraction. In addition, some compounds and corresponding complexes were also assayed in vitro for their ability to inhibit the growth of representative Gram-positive bacteria, Gram-negative bacteria and the fungus. It was worthwhile to note that some compounds could be used as potential antibacterial agents. (C) 2015 Elsevier Ltd. All rights reserved.
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