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N,N'-dimethylethylenediamine bis(methanesulfonic acid)

中文名称
——
中文别名
——
英文名称
N,N'-dimethylethylenediamine bis(methanesulfonic acid)
英文别名
N,N'-dimethylethane-1,2-diamine;methanesulfonic acid
N,N'-dimethylethylenediamine bis(methanesulfonic acid)化学式
CAS
——
化学式
2CH4O3S*C4H12N2
mdl
——
分子量
280.367
InChiKey
DMQKLCBQHMATNW-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):
    -1.07
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    86.8
  • 氢给体数:
    3
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    甲烷磺酸N,N'-二甲基乙二胺乙醇 为溶剂, 反应 0.33h, 以73%的产率得到N,N'-dimethylethylenediamine bis(methanesulfonic acid)
    参考文献:
    名称:
    A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper-Catalyzed C–X Couplings
    摘要:
    A stable adduct of Cul with Bu4NI, soluble in organic solvents, has been identified as an effective catalyst for copper-catalyzed C-N and C-O couplings. In addition, stable nonhygroscopic salts of some high performance ligands (diamine MsOH salts/CuX and copper(II) diketonates) were shown to be of similar and sometimes greater reactivity compared to the literature reagents for these couplings. Furthermore, these more robust conditions result in more reproducible results.
    DOI:
    10.1021/jo300905w
  • 作为试剂:
    描述:
    2-吡咯烷酮1,3-二甲基-5-碘苯 在 bis(tetrapropylammonium) tetraiododicuprate(I) 、 N,N'-dimethylethylenediamine bis(methanesulfonic acid)potassium carbonate 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以88%的产率得到1-(3,5-dimethylphenyl)-1H-pyrrolidin-2-one
    参考文献:
    名称:
    A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper-Catalyzed C–X Couplings
    摘要:
    A stable adduct of Cul with Bu4NI, soluble in organic solvents, has been identified as an effective catalyst for copper-catalyzed C-N and C-O couplings. In addition, stable nonhygroscopic salts of some high performance ligands (diamine MsOH salts/CuX and copper(II) diketonates) were shown to be of similar and sometimes greater reactivity compared to the literature reagents for these couplings. Furthermore, these more robust conditions result in more reproducible results.
    DOI:
    10.1021/jo300905w
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