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1-Benzyl-4-[4-[[12,18,39-tris[[4-(1-benzyltriazol-4-yl)phenoxy]methyl]-25,29,33,37-tetramethyl-2,4,8,10,14,16,20,22-octaoxanonacyclo[21.15.1.124,38.05,36.07,34.011,32.013,30.017,28.019,26]tetraconta-1(39),5,7(34),11,13(30),17(28),18,23,26,31,35,38(40)-dodecaen-6-yl]methoxy]phenyl]triazole | 1451074-90-0

中文名称
——
中文别名
——
英文名称
1-Benzyl-4-[4-[[12,18,39-tris[[4-(1-benzyltriazol-4-yl)phenoxy]methyl]-25,29,33,37-tetramethyl-2,4,8,10,14,16,20,22-octaoxanonacyclo[21.15.1.124,38.05,36.07,34.011,32.013,30.017,28.019,26]tetraconta-1(39),5,7(34),11,13(30),17(28),18,23,26,31,35,38(40)-dodecaen-6-yl]methoxy]phenyl]triazole
英文别名
1-benzyl-4-[4-[[12,18,39-tris[[4-(1-benzyltriazol-4-yl)phenoxy]methyl]-25,29,33,37-tetramethyl-2,4,8,10,14,16,20,22-octaoxanonacyclo[21.15.1.124,38.05,36.07,34.011,32.013,30.017,28.019,26]tetraconta-1(39),5,7(34),11,13(30),17(28),18,23,26,31,35,38(40)-dodecaen-6-yl]methoxy]phenyl]triazole
1-Benzyl-4-[4-[[12,18,39-tris[[4-(1-benzyltriazol-4-yl)phenoxy]methyl]-25,29,33,37-tetramethyl-2,4,8,10,14,16,20,22-octaoxanonacyclo[21.15.1.124,38.05,36.07,34.011,32.013,30.017,28.019,26]tetraconta-1(39),5,7(34),11,13(30),17(28),18,23,26,31,35,38(40)-dodecaen-6-yl]methoxy]phenyl]triazole化学式
CAS
1451074-90-0
化学式
C100H84N12O12
mdl
——
分子量
1645.84
InChiKey
NAPIMVWPGAFITK-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):
    18.2
  • 重原子数:
    124
  • 可旋转键数:
    24
  • 环数:
    21.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    234
  • 氢给体数:
    0
  • 氢受体数:
    20

反应信息

  • 作为产物:
    描述:
    6,12,18,39-Tetrakis[(4-ethynylphenoxy)methyl]-25,29,33,37-tetramethyl-2,4,8,10,14,16,20,22-octaoxanonacyclo[21.15.1.124,38.05,36.07,34.011,32.013,30.017,28.019,26]tetraconta-1(39),5,7(34),11,13(30),17(28),18,23,26,31,35,38(40)-dodecaene 、 苄基叠氮copper(l) iodide三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 以70%的产率得到1-Benzyl-4-[4-[[12,18,39-tris[[4-(1-benzyltriazol-4-yl)phenoxy]methyl]-25,29,33,37-tetramethyl-2,4,8,10,14,16,20,22-octaoxanonacyclo[21.15.1.124,38.05,36.07,34.011,32.013,30.017,28.019,26]tetraconta-1(39),5,7(34),11,13(30),17(28),18,23,26,31,35,38(40)-dodecaen-6-yl]methoxy]phenyl]triazole
    参考文献:
    名称:
    Synthesis of elongated cavitands via click reactions and their use as chemosensors
    摘要:
    A very efficient modular reaction protocol was developed to attach various functionalities to a rigid cavitand scaffold. In this way, aryl, iodoaryl, benzyl, pyrrolidylmethyl groups, as well as a polyethyleneglycol chain were attached to the 'triazol-level' of the cavitand. The palladium-catalyzed ethynylation of the iodoarene moieties, followed by the copper(I)-catalyzed azide-alkyne cycloaddition produced novel cavitands with significantly elongated binding pockets. The dimensions of these molecules are calculated to be at least 9 angstrom x 18 angstrom, which place them amongst the largest unimolecular hosts obtained by pure covalent synthesis. A cavitand-based click conjugate is used for selective complexation of Cu2+ and Fe3+, providing significant fluorescent quenching. (C) 2013 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tet.2013.07.044
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