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3-methyl-1-anthracenamine | 139009-50-0

中文名称
——
中文别名
——
英文名称
3-methyl-1-anthracenamine
英文别名
3-Methylanthracen-1-amine
3-methyl-1-anthracenamine化学式
CAS
139009-50-0
化学式
C15H13N
mdl
——
分子量
207.275
InChiKey
VFFAXRYQUDMLNT-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):
    4.1
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    26
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    1-氨基-3-甲基蒽-9,10-二酮sodium hydroxide 作用下, 反应 24.0h, 以59%的产率得到3-methyl-1-anthracenamine
    参考文献:
    名称:
    Castle, Raymond N.; Kudo, Hirotaka; Lee, Milton L., Collection of Czechoslovak Chemical Communications, 1991, vol. 56, # 11.1, p. 2269 - 2277
    摘要:
    DOI:
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文献信息

  • Polyaminopyridines and method for producing same
    申请人:Kanbara Takaki
    公开号:US20060293503A1
    公开(公告)日:2006-12-28
    The present invention provides novel polyaminopyridines which are excellent in solubility in various solvents, and are preferably used in a polymer-type organic electroluminescent material, and a process for preparing the same. More particularly, the present invention provides polyaminopyridines having a repetition structural unit represented by the following general formula (1); and having a number average molecular weight in a range of 500 to 1000000.
    本发明提供了新型的聚氨基吡啶,其在各种溶剂中具有优异的溶解性,并且最好用于聚合物型有机电致发光材料,并提供了制备它们的过程。更具体地,本发明提供了具有以下一般式(1)所表示的重复结构单元的聚氨基吡啶,其具有500至1000000之间的数均分子量。
  • POLYAMINOPYRIDINES AND METHOD FOR PRODUCING SAME
    申请人:SUMITOMO SEIKA CHEMICALS CO., LTD.
    公开号:EP1669390A1
    公开(公告)日:2006-06-14
    The present invention provides novel polyaminopyridines which are excellent in solubility in various solvents, and are preferably used in a polymer-type organic electroluminescent material, and a process for preparing the same. More particularly, the present invention provides polyaminopyridines having a repetition structural unit represented by the following general formula (1); and having a number average molecular weight in a range of 500 to 1000000.
    本发明提供了在各种溶剂中溶解性极佳的新型聚氨基吡啶,优选用于聚合物型有机电致发光材料,并提供了制备该材料的工艺。更具体地说,本发明提供了具有以下通式(1)所代表的重复结构单元的聚氨基吡啶; 且平均分子量在 500 至 1000000 之间。
  • Chromatographic materials for the separation of unsaturated molecules
    申请人:Waters Technologies Corporation
    公开号:US10092894B2
    公开(公告)日:2018-10-09
    The present disclosure relates to a method of separating a compound of interest, particularly unsaturated compound(s) of interest, from a mixture. The compound is separated using a column having a chromatographic stationary phase material for various different modes of chromatography containing a first substituent and a second substituent. The first substituent minimizes compound retention variation over time under chromatographic conditions. The second substituent chromatographically and selectively retains the compound by incorporating one or more aromatic, polyaromatic, heterocyclic aromatic, or polyheterocyclic aromatic hydrocarbon groups, each group being optionally substituted with an aliphatic group.
    本公开涉及一种从混合物中分离相关化合物,特别是相关不饱和化合物的方法。使用色谱柱分离化合物,该色谱柱具有用于各种不同色谱模式的色谱固定相材料,其中含有第一取代基和第二取代基。在色谱条件下,第一取代基可最大程度地减少化合物保留时间的变化。第二取代基通过加入一个或多个芳香族、多芳香族、杂环芳香族或多杂环芳香族烃基团(每个基团可选择被脂肪族基团取代),在色谱上选择性地保留化合物。
  • CHROMATOGRAPHIC MATERIALS FOR THE SEPARATION OF UNSATURATED MOLECULES
    申请人:Waters Technologies Corporation
    公开号:EP3113857A1
    公开(公告)日:2017-01-11
  • [EN] CHROMOTOGRAPHIC MATERIALS FOR THE SEPARATION OF UNSATURATED MOLECULES<br/>[FR] MATÉRIAUX CHROMATOGRAPHIQUES POUR LA SÉPARATION DE MOLÉCULES INSATURÉES
    申请人:WATERS TECHNOLOGIES CORP
    公开号:WO2015134317A1
    公开(公告)日:2015-09-11
    The present disclosure relates to a method of separating a compound of interest, particularly unsaturated compound(s) of interest, from a mixture. The compound is separated using a column having a chromatographic stationary phase material for various different modes of chromatography containing a first substituent and a second substituent. The first substituent minimizes compound retention variation over time under chromatographic conditions. The second substituent chromatographically and selectively retains the compound by incorporating one or more aromatic, polyaromatic, heterocyclic aromatic, or polyheterocyclic aromatic hydrocarbon groups, each group being optionally substituted with an aliphatic group.
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