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4-[[14,22,26-Tris(4-hydroxyphenoxy)-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),6,8,10,12,14,16,18,20,23-tridecaen-11-yl]oxy]phenol | 402928-20-5

中文名称
——
中文别名
——
英文名称
4-[[14,22,26-Tris(4-hydroxyphenoxy)-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),6,8,10,12,14,16,18,20,23-tridecaen-11-yl]oxy]phenol
英文别名
4-[[14,22,26-tris(4-hydroxyphenoxy)-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),6,8,10,12,14,16,18,20,23-tridecaen-11-yl]oxy]phenol
4-[[14,22,26-Tris(4-hydroxyphenoxy)-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),6,8,10,12,14,16,18,20,23-tridecaen-11-yl]oxy]phenol化学式
CAS
402928-20-5
化学式
C48H28N2O8
mdl
——
分子量
760.759
InChiKey
OYOANIAMHLOINF-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):
    10.7
  • 重原子数:
    58
  • 可旋转键数:
    8
  • 环数:
    11.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    144
  • 氢给体数:
    4
  • 氢受体数:
    10

反应信息

  • 作为反应物:
    描述:
    3,5-didodecyloxybenzoic acid chloride4-[[14,22,26-Tris(4-hydroxyphenoxy)-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),6,8,10,12,14,16,18,20,23-tridecaen-11-yl]oxy]phenol三乙胺 作用下, 以 二氯甲烷 为溶剂, 生成 [4-[[14,22,26-Tris[4-(3,5-didodecoxybenzoyl)oxyphenoxy]-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),6,8,10,12,14,16,18,20,23-tridecaen-11-yl]oxy]phenyl] 3,5-didodecoxybenzoate
    参考文献:
    名称:
    Control of Liquid Crystallinity of Diazadibenzoperylene Dyes by Covalent and Hydrogen-Bonded Attachment of Mesogens We thank P. Zell for his assistance in the practical work, Frau G. Dörfner and Prof. U. Thewalt (Sektion Röntgenbeugung, Universität Ulm) and Dr. B. Heise (Abteilung Experimentelle Physik, Universität Ulm) for X-ray diffraction studies. Financial support from the Deutsche Forschungsgemeinschaft (Habilitandenstipendium for F.W.), the Fonds der Chemischen Industrie (Liebig-Stipendium for F.W.), and the Dr. Otto Röhm Gedächtnisstiftung is gratefully acknowledged.
    摘要:
    DOI:
    10.1002/1521-3773(20011203)40:23<4425::aid-anie4425>3.0.co;2-z
  • 作为产物:
    描述:
    5,6,12,13-Tetrakis-(4-methoxy-phenoxy)-anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline 在 三溴化硼 作用下, 以 二氯甲烷 为溶剂, 以95%的产率得到4-[[14,22,26-Tris(4-hydroxyphenoxy)-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),6,8,10,12,14,16,18,20,23-tridecaen-11-yl]oxy]phenol
    参考文献:
    名称:
    Control of Liquid Crystallinity of Diazadibenzoperylene Dyes by Covalent and Hydrogen-Bonded Attachment of Mesogens We thank P. Zell for his assistance in the practical work, Frau G. Dörfner and Prof. U. Thewalt (Sektion Röntgenbeugung, Universität Ulm) and Dr. B. Heise (Abteilung Experimentelle Physik, Universität Ulm) for X-ray diffraction studies. Financial support from the Deutsche Forschungsgemeinschaft (Habilitandenstipendium for F.W.), the Fonds der Chemischen Industrie (Liebig-Stipendium for F.W.), and the Dr. Otto Röhm Gedächtnisstiftung is gratefully acknowledged.
    摘要:
    DOI:
    10.1002/1521-3773(20011203)40:23<4425::aid-anie4425>3.0.co;2-z
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文献信息

  • Rigid-Rod Metallosupramolecular Polymers of Dendronized Diazadibenzoperylene Dyes
    作者:Frank Würthner、Vladimir Stepanenko、Armin Sautter
    DOI:10.1002/anie.200503717
    日期:2006.3.13
  • Control of Liquid Crystallinity of Diazadibenzoperylene Dyes by Covalent and Hydrogen-Bonded Attachment of Mesogens We thank P. Zell for his assistance in the practical work, Frau G. Dörfner and Prof. U. Thewalt (Sektion Röntgenbeugung, Universität Ulm) and Dr. B. Heise (Abteilung Experimentelle Physik, Universität Ulm) for X-ray diffraction studies. Financial support from the Deutsche Forschungsgemeinschaft (Habilitandenstipendium for F.W.), the Fonds der Chemischen Industrie (Liebig-Stipendium for F.W.), and the Dr. Otto Röhm Gedächtnisstiftung is gratefully acknowledged.
    作者:Armin Sautter、Christoph Thalacker、Frank Würthner
    DOI:10.1002/1521-3773(20011203)40:23<4425::aid-anie4425>3.0.co;2-z
    日期:2001.12.3
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