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1,11-dinitro-3,6,9-trioxaundecane | 203740-62-9

中文名称
——
中文别名
——
英文名称
1,11-dinitro-3,6,9-trioxaundecane
英文别名
1-Nitro-2-[2-[2-(2-nitroethoxy)ethoxy]ethoxy]ethane
1,11-dinitro-3,6,9-trioxaundecane化学式
CAS
203740-62-9
化学式
C8H16N2O7
mdl
——
分子量
252.224
InChiKey
ZYZZHFWJVWGQCI-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:
    390.8±37.0 °C(Predicted)
  • 密度:
    1.228±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.6
  • 重原子数:
    17
  • 可旋转键数:
    10
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    119
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Organic metal-complexes. XXI. Synthesis and structure of 3,5,15,17-tetraoxo-1,7,10,13,19,22-hexaoxa-cyclotetracosane and 2,12,14,24-tetraoxo-4,7,10,16,19,22-hexaoxa-25-mercurato-bicyclo[11.11.1]pentacosane
    摘要:
    A new synthesis of the title crown via isoxazolo crown ether 7 and macrocyclic bis-peneaminoketone 10 is described. 7 can be synthesized in 14% yield by a non-template double-[3+2] cycloaddition of dinitrileoxide 5 prepared in situ from dinitropolyether 19 by dehydration with Ph-NCO and alkyne 6. The compounds 16, 17 and 18 are synthesized by the same synthetic strategy. Comparable IR and H-1 NMR spectroscopic data of macrocyclic and non-cyclic compounds show, that macrocyclic conformation stabilizing effects can be ruled out. The structures of the macrocycles 1, 7, 10 and that of the Hg(II)-complex 25, synthesized by reaction of 1 with Hg(OAc)(2) were established by single-crystal X-ray structure analyses. Both inter-and intramolecular hydrogen bonds are observed for the macrocyclic bis-beta-eneaminoketone 10, whereas only intramolecular hydrogen bonds are formed by 1. In the Hg(II)-complex of 1 the mercury is bonded to two methylene groups. C-Hg-C is almost linear [177(1)degrees], the mean Hg-C distance amounts to 215(1) pm. In addition to the Hg-C bonds, each Hg makes a short contact to a carbonyl oxygen in a neighbouring molecule in the plane perpendicular to the C-Hg-C axis [Hg(1)-O(1) = 279(1) pm, Hg(2)-O(5)= 284(1) pm].
    DOI:
    10.1002/prac.19983400207
  • 作为产物:
    参考文献:
    名称:
    Organic metal-complexes. XXI. Synthesis and structure of 3,5,15,17-tetraoxo-1,7,10,13,19,22-hexaoxa-cyclotetracosane and 2,12,14,24-tetraoxo-4,7,10,16,19,22-hexaoxa-25-mercurato-bicyclo[11.11.1]pentacosane
    摘要:
    A new synthesis of the title crown via isoxazolo crown ether 7 and macrocyclic bis-peneaminoketone 10 is described. 7 can be synthesized in 14% yield by a non-template double-[3+2] cycloaddition of dinitrileoxide 5 prepared in situ from dinitropolyether 19 by dehydration with Ph-NCO and alkyne 6. The compounds 16, 17 and 18 are synthesized by the same synthetic strategy. Comparable IR and H-1 NMR spectroscopic data of macrocyclic and non-cyclic compounds show, that macrocyclic conformation stabilizing effects can be ruled out. The structures of the macrocycles 1, 7, 10 and that of the Hg(II)-complex 25, synthesized by reaction of 1 with Hg(OAc)(2) were established by single-crystal X-ray structure analyses. Both inter-and intramolecular hydrogen bonds are observed for the macrocyclic bis-beta-eneaminoketone 10, whereas only intramolecular hydrogen bonds are formed by 1. In the Hg(II)-complex of 1 the mercury is bonded to two methylene groups. C-Hg-C is almost linear [177(1)degrees], the mean Hg-C distance amounts to 215(1) pm. In addition to the Hg-C bonds, each Hg makes a short contact to a carbonyl oxygen in a neighbouring molecule in the plane perpendicular to the C-Hg-C axis [Hg(1)-O(1) = 279(1) pm, Hg(2)-O(5)= 284(1) pm].
    DOI:
    10.1002/prac.19983400207
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文献信息

  • Organic metal-complexes. XXI. Synthesis and structure of 3,5,15,17-tetraoxo-1,7,10,13,19,22-hexaoxa-cyclotetracosane and 2,12,14,24-tetraoxo-4,7,10,16,19,22-hexaoxa-25-mercurato-bicyclo[11.11.1]pentacosane
    作者:Wolfram V. Eichinger、Hans Musso、Klaus D. Eichhorn、G�nter Mattern
    DOI:10.1002/prac.19983400207
    日期:——
    A new synthesis of the title crown via isoxazolo crown ether 7 and macrocyclic bis-peneaminoketone 10 is described. 7 can be synthesized in 14% yield by a non-template double-[3+2] cycloaddition of dinitrileoxide 5 prepared in situ from dinitropolyether 19 by dehydration with Ph-NCO and alkyne 6. The compounds 16, 17 and 18 are synthesized by the same synthetic strategy. Comparable IR and H-1 NMR spectroscopic data of macrocyclic and non-cyclic compounds show, that macrocyclic conformation stabilizing effects can be ruled out. The structures of the macrocycles 1, 7, 10 and that of the Hg(II)-complex 25, synthesized by reaction of 1 with Hg(OAc)(2) were established by single-crystal X-ray structure analyses. Both inter-and intramolecular hydrogen bonds are observed for the macrocyclic bis-beta-eneaminoketone 10, whereas only intramolecular hydrogen bonds are formed by 1. In the Hg(II)-complex of 1 the mercury is bonded to two methylene groups. C-Hg-C is almost linear [177(1)degrees], the mean Hg-C distance amounts to 215(1) pm. In addition to the Hg-C bonds, each Hg makes a short contact to a carbonyl oxygen in a neighbouring molecule in the plane perpendicular to the C-Hg-C axis [Hg(1)-O(1) = 279(1) pm, Hg(2)-O(5)= 284(1) pm].
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