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C-1-naphthylresorcin[4]arene | 916134-80-0

中文名称
——
中文别名
——
英文名称
C-1-naphthylresorcin[4]arene
英文别名
2,8,14,20-Tetranaphthalen-1-ylpentacyclo[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-4,6,10,12,16,18,22,24-octol
C-1-naphthylresorcin[4]arene化学式
CAS
916134-80-0
化学式
C68H48O8
mdl
——
分子量
993.124
InChiKey
CDBKFJRTJGTVJU-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):
    15.7
  • 重原子数:
    76
  • 可旋转键数:
    4
  • 环数:
    13.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    162
  • 氢给体数:
    8
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    C-1-naphthylresorcin[4]arene 作用下, 以 为溶剂, 反应 0.5h, 以45.7%的产率得到4,6,10,12,16,18,22,24-octaamino-2,8,14,20-tetra(1-naphthyl)pentacyclo[19.3.1.1(3.7).1(9.13).1(15.19)]octacosa-1(25),3,5,7(28),9,11,13(27),15,17,19(26),21,23-dodecane
    参考文献:
    名称:
    Amination of calix[4]resorcinarenes. First synthesis of calix[4]phenylenediamines
    摘要:
    DOI:
    10.1134/s1070363210030333
  • 作为产物:
    描述:
    1-萘甲醛间苯二酚盐酸 作用下, 以 乙醇 为溶剂, 反应 8.0h, 生成 C-1-naphthylresorcin[4]arene
    参考文献:
    名称:
    Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
    摘要:
    合成并表征了十三种芳基取代的焦高酚[4]芳烃和间苯二酚[4]芳烃结构。系统地研究和讨论了不同芳基侧链对π-π距离、侧链-R基团的内倾角、侧链-R基团的扭曲角度以及侧链-R基团之间角度的影响。
    DOI:
    10.1039/c5ce01792k
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文献信息

  • Regioselective Synthesis and Structure of New Oligophosphorylated <i>rctt</i> Resorcinarenes
    作者:Vera I. Maslennikova、Olga S. Serkova、Tatiana V. Guzeeva、Konstantin A. Lyssenko、Irina I. Levina、Valentina V. Glushko、Eduard E. Nifantyev
    DOI:10.1080/10426507.2010.531489
    日期:2011.8.1
  • Pre-organized oligomodified resorcinarene ligands. Preparation, structure, and complex formation
    作者:O. S. Serkova、A. V. Burikhina、L. K. Vasyanina、O. S. Kuprina、V. I. Maslennikova、E. E. Nifantiev
    DOI:10.1134/s1070363214040240
    日期:2014.4
    Interaction of various conformations of resorcinarenes with carbamoyl chloride, thiocarbamoyl chloride, and trifluoromethanesulfonic acid anhydride has resulted in a series of derivatives with certain pre-organization of the macrocyclic scaffold and the immobilized electron-donating groups. Complex formation of the selected prepared compounds towards Pd(II) derivatives has been studied.
  • PROCESS FOR PRODUCING CARBON MATERIAL
    申请人:Suzuki Junji
    公开号:US20100298522A1
    公开(公告)日:2010-11-25
    A process for producing a carbon material comprising the following steps (A) and (B): Step (A): a step of reacting a compound represented by the formula (1): wherein R represents a hydrogen atom etc., R′ represents a hydrogen atom etc., and n represents 3, 5 or 7, with an aldehyde compound to obtain a polymer, Step (B): a step of heating the polymer obtained in Step (A) at 600 to 3000° C. under an inert gas atmosphere.
  • [EN] PROCESS FOR PRODUCING CARBON MATERIAL<br/>[FR] PROCÉDÉ DE FABRICATION D'UNE MATIÈRE CARBONÉE
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2009101947A2
    公开(公告)日:2009-08-20
    A process for producing a carbon material comprising the following steps (A) and (B): Step (A): a step of reacting a compound represented by the formula (1): wherein R represents a hydrogen atom etc., R' represents a hydrogen atom etc., and n represents 3, 5 or 7, with an aldehyde compound to obtain a polymer, Step (B): a step of heating the polymer obtained in Step (A) at 600 to 3000oC under an inert gas atmosphere.
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