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3,6-bis-(3-methyl-1-butyloxy)-naphthalene-2,7-disulfonyl dichloride | 1116341-15-1

中文名称
——
中文别名
——
英文名称
3,6-bis-(3-methyl-1-butyloxy)-naphthalene-2,7-disulfonyl dichloride
英文别名
3,6-Bis(3-methylbutoxy)naphthalene-2,7-disulfonyl chloride;3,6-bis(3-methylbutoxy)naphthalene-2,7-disulfonyl chloride
3,6-bis-(3-methyl-1-butyloxy)-naphthalene-2,7-disulfonyl dichloride化学式
CAS
1116341-15-1
化学式
C20H26Cl2O6S2
mdl
——
分子量
497.461
InChiKey
WSUAHBCQLMOAOU-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):
    6.5
  • 重原子数:
    30
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    104
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3,6-bis-(3-methyl-1-butyloxy)-naphthalene-2,7-disulfonyl dichloride2,7-二羟基萘三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以15.5%的产率得到5,9,23,27-Tetrakis(3-methylbutoxy)-2,12,20,30-tetraoxa-3lambda6,11lambda6,21lambda6,29lambda6-tetrathianonacyclo[29.5.3.34,10.313,19.322,28.034,38.07,47.016,44.025,41]octatetraconta-1(37),4(48),5,7,9,13(45),14,16(44),17,19(43),22,24,26,28(40),31(39),32,34(38),35,41,46-icosaene 3,3,11,11,21,21,29,29-octaoxide
    参考文献:
    名称:
    One-Pot Formation and Characterization of Macrocyclic Aromatic Tetrasulfonates
    摘要:
    Aromatic tetrasulfonate macrocycles were prepared in one pot by treating arenedisulfonyl chlorides with dihydroxyarenes. X-ray structures revealed that these cyclic molecules have noncollapsible cavities and well-defined conformations resembling the cone and partial cone conformations of calix[4]arenes. Incorporating aromatic residues of different sizes leads to macrocycles with different cavity sizes.
    DOI:
    10.1021/ol8028884
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文献信息

  • One-Pot Formation and Characterization of Macrocyclic Aromatic Tetrasulfonates
    作者:Mingwei Geng、Dechun Zhang、Xiangxiang Wu、Lan He、Bing Gong
    DOI:10.1021/ol8028884
    日期:2009.2.19
    Aromatic tetrasulfonate macrocycles were prepared in one pot by treating arenedisulfonyl chlorides with dihydroxyarenes. X-ray structures revealed that these cyclic molecules have noncollapsible cavities and well-defined conformations resembling the cone and partial cone conformations of calix[4]arenes. Incorporating aromatic residues of different sizes leads to macrocycles with different cavity sizes.
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