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3,4-dihydro-3-azaphenanthrene-4-one | 29108-63-2

中文名称
——
中文别名
——
英文名称
3,4-dihydro-3-azaphenanthrene-4-one
英文别名
benzo[h]isoquinolin-1(2H)-one;benzo[h]isoquinolin-1-one;1,2-Dihydrobenzoisochinolin-1-on;4-Keto-3,4-dihydro-3-aza-phenanthren;2H-benzo[h]isoquinolin-1-one;1,2-dihydrobenz[1,2-h]isoquinolin-1-one;3,4-Dihydro-3-azaphenanthren-4-on;Benzoisoquinolone;2H-benzo[h]isoquinolin-1-one
3,4-dihydro-3-azaphenanthrene-4-one化学式
CAS
29108-63-2
化学式
C13H9NO
mdl
——
分子量
195.221
InChiKey
RGAMLRMKIJBQGL-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

物化性质

  • 熔点:
    200-201 °C
  • 沸点:
    476.3±38.0 °C(Predicted)
  • 密度:
    1.249±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Divergent Synthesis of Isoquinolone and Isocoumarin Derivatives by the Annulation of Benzoic Acid with <i>N</i>-Vinyl Amide
    作者:Rui Sun、Xiao Yang、Qianggen Li、Ke Xu、Juan Tang、Xueli Zheng、Maolin Yuan、Haiyan Fu、Ruixiang Li、Hua Chen
    DOI:10.1021/acs.orglett.9b03638
    日期:2019.12.6
    A simple and efficient method for the synthesis of isoquinolone and isocoumarin derivatives is reported. The method for the first time provides a one-step divergent synthesis of important isoquinolone and isocoumarin skeletons from benzoic acid by switching the coupling partners. In addition, a reliable mechanism has been proposed on the basis of experimental investigations, including kinetic isotope
    报道了一种简单有效的合成异喹诺酮和异香豆素衍生物的方法。该方法首次通过切换偶联伙伴,从苯甲酸一步一步地合成了重要的异喹诺酮和异香豆素骨架。此外,在实验研究的基础上,提出了一种可靠的机制,包括动力学同位素效应实验,13C标记实验,时间跟踪实验和竞争实验,以及DFT计算研究。
  • BLOCK COPOLYMERS FOR STABLE MICELLES
    申请人:Intezyne Technologies, Inc.
    公开号:US20130280306A1
    公开(公告)日:2013-10-24
    The present invention relates to the field of polymer chemistry and more particularly to multiblock copolymers and micelles comprising the same. Compositions herein are useful for drug-delivery applications.
    本发明涉及聚合物化学领域,更具体地说是涉及多区块共聚物以及包含相同的多区块共聚物胶束。本发明的组合物适用于药物输送应用。
  • HYBRID BLOCK COPOLYMER MICELLES WITH MIXED STEREOCHEMISTRY FOR ENCAPSULATION OF HYDROPHOBIC AGENTS
    申请人:SILL Kevin N.
    公开号:US20080274173A1
    公开(公告)日:2008-11-06
    The present invention relates to the field of polymer chemistry and more particularly to multiblock copolymers and micelles comprising the same.
    本发明涉及聚合物化学领域,更具体地说是涉及多嵌段共聚物以及包含该共聚物的胶束。
  • Modular Synthesis of Organoboron Helically Chiral Compounds: Cutouts from Extended Helices
    作者:Julian Full、Santosh P. Panchal、Julian Götz、Ana‐Maria Krause、Agnieszka Nowak‐Król
    DOI:10.1002/anie.202014138
    日期:2021.2.19
    Two types of helically chiral compounds bearing one and two boron atoms were synthesized by a modular approach. Formation of the helical scaffolds was executed by the introduction of boron to flexible biaryl and triaryl derived from small achiral building blocks. All‐ortho‐fused azabora[7]helicenes feature exceptional configurational stability, blue or green fluorescence with quantum yields (Φfl) of
    通过模块化方法合成了两种带有一个和两个硼原子的螺旋手性化合物。通过将硼引入源自小的非手性结构单元的柔性联芳基和三芳基来形成螺旋支架。全邻位稠合azabora[7]螺旋烯具有优异的构型稳定性,溶液中量子产率(Φfl )为18-24%的蓝色或绿色荧光,绿色或黄色固态发射(Φfl高达23%),以及具有高达1.12×10 -2的大不对称因子的强手性光学响应。由成角度和线性稠合的环组成的Azabora[9]螺旋烯是蓝色发射体,其在CH 2 Cl 2中的Φ fl高达47% ,在固态下高达25%。DFT 计算表明,它们的 P-M 互变途径比H1更复杂。单晶 X 射线分析显示甲基和苯基衍生物的堆积排列存在明显差异。这些分子被认为是延伸螺旋的一级结构。
  • [EN] BENZOISOQUINOLINONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS<br/>[FR] MODULATEURS ALLOSTÉRIQUES POSITIFS DU RÉCEPTEUR M1 DE BENZOISOQUINOLINE
    申请人:MERCK SHARP & DOHME
    公开号:WO2018005249A1
    公开(公告)日:2018-01-04
    The present invention is directed to substituted benzoisoquinolinone compounds, their salts, pharmaceutical compositions comprising them and their use in therapy. In particular, the invention is directed substituted benzoisoquinolinone compounds which are muscarinic M1 receptor positive allosteric modulators. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which M1 receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which M1 receptors are involved.
    本发明涉及替代苯并异喹啉酮化合物、它们的盐、包含它们的药物组合物以及它们在治疗中的用途。具体来说,该发明涉及替代苯并异喹啉酮化合物,这些化合物是肌胆碱M1受体阳性变构调节剂。本发明还涉及所述化合物在潜在治疗或预防M1受体参与的神经和精神障碍和疾病中的用途。本发明还涉及包含这些化合物的组合物。本发明还涉及这些组合物在潜在预防或治疗M1受体参与的疾病中的用途。
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