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(E)-1-(9-anthryl)-3-(1-naphthyl)prop-2-en-1-one | 174708-36-2

中文名称
——
中文别名
——
英文名称
(E)-1-(9-anthryl)-3-(1-naphthyl)prop-2-en-1-one
英文别名
(E)-1-anthracen-9-yl-3-naphthalen-1-ylprop-2-en-1-one
(E)-1-(9-anthryl)-3-(1-naphthyl)prop-2-en-1-one化学式
CAS
174708-36-2
化学式
C27H18O
mdl
——
分子量
358.439
InChiKey
DRDSKIVQVGTMBW-WUKNDPDISA-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):
    7.4
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    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:
    (E)-1-(9-anthryl)-3-(1-naphthyl)prop-2-en-1-one 在 sodium tetrahydroborate 作用下, 以 1,4-二氧六环甲醇 为溶剂, 生成 1-(9-anthryl)-3-(1-naphthyl)propan-1-ol
    参考文献:
    名称:
    Chiral recognition and molecular interaction in cellulose derivatives
    摘要:
    Nineteen 1,3-bis(aryl)propane derivatives and six model compounds with a single chromophore were used to explore the chiral discrimination ability of cellulose derivatives, in particular cellulose triphenylcarbamate (CTC), in connection with the mode of interaction of these probe molecules with adsorbents. The interaction was evaluated by conformational analysis of the probe molecules and circular dichroism. Thc 1,3-bis(aryl)propanes with 9-anthryl moieties possessed a highly limited conformation owing to thc bulky substituent and hardly changed their shape on CTC as evidenced by CD spectra; thus, they may be regarded as ''rigid'' substrates. However, these ''rigid'' substrates were resolved quite effectively. On the other hand, those with 2-naphthyl moieties possessed a number of stable conformations and could change their shape in diastereomeric complexes on CTC; thus, they may be assumed as ''soft'' substrates, against which the chiral discrimination was inefficient. The present study revealed that the optical resolution may be interpreted at least partly in terms of the ''rigid'' and ''soft'' concept.
    DOI:
    10.1021/j100193a020
  • 作为产物:
    参考文献:
    名称:
    Chiral recognition and molecular interaction in cellulose derivatives
    摘要:
    Nineteen 1,3-bis(aryl)propane derivatives and six model compounds with a single chromophore were used to explore the chiral discrimination ability of cellulose derivatives, in particular cellulose triphenylcarbamate (CTC), in connection with the mode of interaction of these probe molecules with adsorbents. The interaction was evaluated by conformational analysis of the probe molecules and circular dichroism. Thc 1,3-bis(aryl)propanes with 9-anthryl moieties possessed a highly limited conformation owing to thc bulky substituent and hardly changed their shape on CTC as evidenced by CD spectra; thus, they may be regarded as ''rigid'' substrates. However, these ''rigid'' substrates were resolved quite effectively. On the other hand, those with 2-naphthyl moieties possessed a number of stable conformations and could change their shape in diastereomeric complexes on CTC; thus, they may be assumed as ''soft'' substrates, against which the chiral discrimination was inefficient. The present study revealed that the optical resolution may be interpreted at least partly in terms of the ''rigid'' and ''soft'' concept.
    DOI:
    10.1021/j100193a020
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文献信息

  • Nitrogenous heterocyclic derivative and organic elecrtroluminescent element employing the same
    申请人:Yamamoto Hiroshi
    公开号:US20060154105A1
    公开(公告)日:2006-07-13
    A specific derivative of heterocyclic compound having nitrogen atom and an organic electroluminescence device comprising the compound. An organic electroluminescence device comprising at least one of organic compound layers including a light emitting layer sandwiched between an anode and a cathode, wherein said at least one of the organic compound layers comprises the derivative of the heterocyclic compound having nitrogen atom as a sole component or as mixed component. The organic electroluminescence device achieves elevation of luminance and excellent efficiency of light emission, and also achieves long lifetime by an improvement of an electrode adhesion.
    一种具有氮原子的杂环化合物的特定衍生物,以及包括该化合物的有机电致发光装置。该有机电致发光装置包括至少一个有机化合物层,其中包括在阳极和阴极之间的发光层,其中该至少一个有机化合物层包括作为唯一组分或混合组分的具有氮原子的杂环化合物的衍生物。该有机电致发光装置实现了亮度的提高和优秀的发光效率,并通过改善电极粘附实现了长寿命。
  • NITROGENOUS HETEROCYCLIC DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT EMPLOYING THE SAME
    申请人:IDEMITSU KOSAN CO., LTD.
    公开号:EP1582516A1
    公开(公告)日:2005-10-05
    A specific derivative of heterocyclic compound having nitrogen atom and an organic electroluminescence device comprising the compound. An organic electroluminescence device comprising at least one of organic compound layers including a light emitting layer sandwiched between an anode and a cathode, wherein said at least one of the organic compound layers comprises the derivative of the heterocyclic compound having nitrogen atom as a sole component or as mixed component. The organic electroluminescence device achieves elevation of luminance and excellent efficiency of light emission, and also achieves long lifetime by an improvement of an electrode adhesion.
    一种具有氮原子的杂环化合物的特定衍生物和一种包含该化合物的有机电致发光器件。一种有机电致发光器件,包括至少一个有机化合物层,其中包括夹在阳极和阴极之间的发光层,其中所述至少一个有机化合物层包括作为唯一成分或混合成分的具有氮原子的杂环化合物的衍生物。该有机电致发光器件不仅提高了亮度和发光效率,还通过改善电极附着力延长了使用寿命。
  • US7867629B2
    申请人:——
    公开号:US7867629B2
    公开(公告)日:2011-01-11
  • Chiral recognition and molecular interaction in cellulose derivatives
    作者:Kenji Itoh、Tomiki Ikeda、Shigeo Tazuke、Tohru Shibata
    DOI:10.1021/j100193a020
    日期:1992.7
    Nineteen 1,3-bis(aryl)propane derivatives and six model compounds with a single chromophore were used to explore the chiral discrimination ability of cellulose derivatives, in particular cellulose triphenylcarbamate (CTC), in connection with the mode of interaction of these probe molecules with adsorbents. The interaction was evaluated by conformational analysis of the probe molecules and circular dichroism. Thc 1,3-bis(aryl)propanes with 9-anthryl moieties possessed a highly limited conformation owing to thc bulky substituent and hardly changed their shape on CTC as evidenced by CD spectra; thus, they may be regarded as ''rigid'' substrates. However, these ''rigid'' substrates were resolved quite effectively. On the other hand, those with 2-naphthyl moieties possessed a number of stable conformations and could change their shape in diastereomeric complexes on CTC; thus, they may be assumed as ''soft'' substrates, against which the chiral discrimination was inefficient. The present study revealed that the optical resolution may be interpreted at least partly in terms of the ''rigid'' and ''soft'' concept.
  • Mori, Yukie; Maeda, Koko, Journal of the Chemical Society. Perkin transactions II, 1996, p. 113 - 120
    作者:Mori, Yukie、Maeda, Koko
    DOI:——
    日期:——
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