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N,N'-bis(2-methyl-6-hepten-2-yl)sulfamide | 143958-77-4

中文名称
——
中文别名
——
英文名称
N,N'-bis(2-methyl-6-hepten-2-yl)sulfamide
英文别名
2-methyl-N-(2-methylhept-6-en-2-ylsulfamoyl)hept-6-en-2-amine
N,N'-bis(2-methyl-6-hepten-2-yl)sulfamide化学式
CAS
143958-77-4
化学式
C16H32N2O2S
mdl
——
分子量
316.508
InChiKey
NIGREJBOSICFMW-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

物化性质

  • 沸点:
    408.4±48.0 °C(Predicted)
  • 密度:
    0.984±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    21
  • 可旋转键数:
    12
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    66.6
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    N,N'-bis(2-methyl-6-hepten-2-yl)sulfamide次氯酸叔丁酯 、 sodium hydride 作用下, 以 乙醚 为溶剂, 反应 9.0h, 生成 2-methyl-hepta-1,6-diene
    参考文献:
    名称:
    Attempts to trap radicals formed in solution by a magnesium surface
    摘要:
    The synthesis of 2,2-azo-2-methyl-6-heptene (1) is described. Photolytic decomposition of 1 in ether gave rise to the 1,1-dimethyl-5-hexenyl radical clock (2) which yielded 1,1,2-trimethylcyclopentane (3), 6-methyl-1-heptene (4), and 2-methyl-1,6-heptadiene (5) in the ratio of 1:0.72:0.56, respectively. The ratio did not change appreciably when a well-stirred mixture of 1 and 5 equiv of magnesium powder was photolyzed. Moreover, the solution gave a negative test (2,2'-biquinoline) for the presence of Grignard reagent. Thus, it has been experimentally demonstrated that the radicals formed in solution do not react with a magnesium surface to form Grignard reagents.
    DOI:
    10.1021/jo00049a026
  • 作为产物:
    参考文献:
    名称:
    Attempts to trap radicals formed in solution by a magnesium surface
    摘要:
    The synthesis of 2,2-azo-2-methyl-6-heptene (1) is described. Photolytic decomposition of 1 in ether gave rise to the 1,1-dimethyl-5-hexenyl radical clock (2) which yielded 1,1,2-trimethylcyclopentane (3), 6-methyl-1-heptene (4), and 2-methyl-1,6-heptadiene (5) in the ratio of 1:0.72:0.56, respectively. The ratio did not change appreciably when a well-stirred mixture of 1 and 5 equiv of magnesium powder was photolyzed. Moreover, the solution gave a negative test (2,2'-biquinoline) for the presence of Grignard reagent. Thus, it has been experimentally demonstrated that the radicals formed in solution do not react with a magnesium surface to form Grignard reagents.
    DOI:
    10.1021/jo00049a026
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文献信息

  • Attempts to trap radicals formed in solution by a magnesium surface
    作者:H. M. Walborsky、M. Topolski、C. Hamdouchi、J. Pankowski
    DOI:10.1021/jo00049a026
    日期:1992.11
    The synthesis of 2,2-azo-2-methyl-6-heptene (1) is described. Photolytic decomposition of 1 in ether gave rise to the 1,1-dimethyl-5-hexenyl radical clock (2) which yielded 1,1,2-trimethylcyclopentane (3), 6-methyl-1-heptene (4), and 2-methyl-1,6-heptadiene (5) in the ratio of 1:0.72:0.56, respectively. The ratio did not change appreciably when a well-stirred mixture of 1 and 5 equiv of magnesium powder was photolyzed. Moreover, the solution gave a negative test (2,2'-biquinoline) for the presence of Grignard reagent. Thus, it has been experimentally demonstrated that the radicals formed in solution do not react with a magnesium surface to form Grignard reagents.
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