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dimethyl 1(4),1(6),5(4),5(6)-tetra-tert-butyl-3(4),3(6),7(4),7(6)-tetranitro-2,4,6,8-tetraoxa-1,3,5,7(1,3)-tetrabenzenacyclooctaphane-1(2),5(2)-dicarboxylate | 1201827-01-1

中文名称
——
中文别名
——
英文名称
dimethyl 1(4),1(6),5(4),5(6)-tetra-tert-butyl-3(4),3(6),7(4),7(6)-tetranitro-2,4,6,8-tetraoxa-1,3,5,7(1,3)-tetrabenzenacyclooctaphane-1(2),5(2)-dicarboxylate
英文别名
Dimethyl 10,12,22,24-tetratert-butyl-4,6,16,18-tetranitro-2,8,14,20-tetraoxapentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(25),3(28),4,6,9(27),10,12,15,17,19(26),21,23-dodecaene-25,27-dicarboxylate;dimethyl 10,12,22,24-tetratert-butyl-4,6,16,18-tetranitro-2,8,14,20-tetraoxapentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(25),3(28),4,6,9(27),10,12,15,17,19(26),21,23-dodecaene-25,27-dicarboxylate
dimethyl 1(4),1(6),5(4),5(6)-tetra-tert-butyl-3(4),3(6),7(4),7(6)-tetranitro-2,4,6,8-tetraoxa-1,3,5,7(1,3)-tetrabenzenacyclooctaphane-1(2),5(2)-dicarboxylate化学式
CAS
1201827-01-1
化学式
C44H48N4O16
mdl
——
分子量
888.882
InChiKey
FGEYAOMNKAPCRB-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):
    11.8
  • 重原子数:
    64
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    288
  • 氢给体数:
    0
  • 氢受体数:
    16

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    1,5-二氟-2,4-二硝基苯methyl 3,5-di-tert-butyl-2,6-dihydroxybenzoate 在 cesium fluoride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以49%的产率得到dimethyl 1(4),1(6),5(4),5(6)-tetra-tert-butyl-3(4),3(6),7(4),7(6)-tetranitro-2,4,6,8-tetraoxa-1,3,5,7(1,3)-tetrabenzenacyclooctaphane-1(2),5(2)-dicarboxylate
    参考文献:
    名称:
    Synthesis and solid state structure of oxacalix[4]arenes bearing four nitro groups and four tert-butyl groups at their extra-annular positions
    摘要:
    Four oxacalix[4]arene derivatives, in which 1,3-dinitrobenzene units and 13-di-tert-butylbenzene units are incorporated in alternating order, were synthesized by aromatic nucleophilic substitution. The introduction of the tert-butyl groups increased the stability of the macrocycles against nucleophilic C-O bond cleavage. X-ray crystal structure analyses reveal that the oxacalixarenes adopt an unsymmetrical 13-alternate conformation. The bulky substituents did not disturb the conjugation between the bridging oxygen atoms and the dinitrobenzene rings. (C) 2009 Elsevier Ltd. All rights reserved,
    DOI:
    10.1016/j.tet.2009.09.116
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文献信息

  • Synthesis and solid state structure of oxacalix[4]arenes bearing four nitro groups and four tert-butyl groups at their extra-annular positions
    作者:Shuichiro Akagi、Yusuke Yasukawa、Kazuhiro Kobayashi、Hisatoshi Konishi
    DOI:10.1016/j.tet.2009.09.116
    日期:2009.11
    Four oxacalix[4]arene derivatives, in which 1,3-dinitrobenzene units and 13-di-tert-butylbenzene units are incorporated in alternating order, were synthesized by aromatic nucleophilic substitution. The introduction of the tert-butyl groups increased the stability of the macrocycles against nucleophilic C-O bond cleavage. X-ray crystal structure analyses reveal that the oxacalixarenes adopt an unsymmetrical 13-alternate conformation. The bulky substituents did not disturb the conjugation between the bridging oxygen atoms and the dinitrobenzene rings. (C) 2009 Elsevier Ltd. All rights reserved,
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