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1-phenyl-1,2-dihydrobenzo[f]quinolin-3(4H)-one | 64257-37-0

中文名称
——
中文别名
——
英文名称
1-phenyl-1,2-dihydrobenzo[f]quinolin-3(4H)-one
英文别名
1-phenyl-1,4-dihydrobenzo[f]quinolin-3(2H)-one;1-phenyl-2,4-dihydro-1H-benzo[f]quinolin-3-one
1-phenyl-1,2-dihydrobenzo[f]quinolin-3(4H)-one化学式
CAS
64257-37-0
化学式
C19H15NO
mdl
——
分子量
273.334
InChiKey
TZTZRPKCJWDRQQ-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):
    3.8
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

上下游信息

  • 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

  • Three Component One-Pot Synthesis of 1-Aryl-4-benzo[f]quinoline Derivatives in Glycerol
    作者:Xue-Mei Wang、Xin Ma、Hai-Long Ma
    DOI:10.14233/ajchem.2015.18100
    日期:——
    A series of 1-aryl-1,2-dihydrobenzo[f]quinolin-3(4H)one derivatives were synthesized by one-pot muticomponent reaction of Meldrums acid with benzaldehyde, naphthalene-2-amine in glycerol. Glycerol, a new green organic solvent, it not only acts as a catalyst but also as a recyclable solvent by significantly enhancing the intramolecular cyclization. When compared with classical methods, this method has the advantages of milder reaction conditions, good yields, easy processing and environmental benignity. All compounds were characterized by elemental analysis, FT-IR and 1H NMR spectra.
    在甘油中,通过梅氏酸与苯甲醛、萘-2-胺的单锅突变组分反应,合成了一系列 1-芳基-1,2-二氢苯并[f]喹啉-3(4H)-1 衍生物。甘油是一种新型的绿色有机溶剂,它不仅可以作为催化剂,还可以作为可回收溶剂,显著提高分子内环化作用。与传统方法相比,该方法具有反应条件温和、产率高、易于加工和环保等优点。所有化合物都通过元素分析、傅立叶变换红外光谱和 1H NMR 光谱进行了表征。
  • One-pot synthesis of benzoquinoline and coumarin derivatives using Meldrum’s acid in three-component reactions
    作者:Xue-Mei Wang、He-Lin Ye、Zheng-Jun Qaun、Xi-Cun Wang
    DOI:10.1007/s11164-012-0762-z
    日期:2013.7
    A series of 1-aryl-1,2-dihydrobenzo[f]quinolin-3(4H)-one derivatives and 4-aryl-7,7-dimethyl-5-oxo-3,4,5,6,7,8-hexahydrocoumarin derivatives have been synthesized by one-pot multicomponent reaction of Meldrum’s acid with benzaldehyde, naphthalene-2-amine, or cyclohexanedione in PEG-400. The method has the advantages of mild reaction conditions, good yields, and easy processing, and is environmentally
    一系列1-芳基-1,2-二氢苯并[ f ]喹啉-3(4 H)-一衍生物和4-芳基-7,7-二甲基-5-氧代-3,4,5,6,7,通过Meldrum的酸与苯甲醛,萘-2-胺或环己二酮在PEG-400中的一锅多组分反应合成了8-六氢香豆素衍生物。该方法的优点是反应条件温和,收率好,易加工,对环境无害。
  • Compounds, Compositions and Methods of Inhibiting Alpha-Synuclein Toxicity
    申请人:Lindquist Susan L.
    公开号:US20080261953A1
    公开(公告)日:2008-10-23
    Compounds and compositions are provided for treatment or amelioration of one or more symptoms of α-synuclein toxicity, α-synuclein mediated diseases or diseases in which α-synuclein fibrils are a symptom or cause of the disease. In one embodiment, the compounds for use in the compositions and methods are heteroaryl acylguanidines, heteroarylhydrazones, dihy-dropyridones, heteroaryl and aryl styryl ketones, and heteroarylpyrazoles.
    提供了化合物和组合物,用于治疗或缓解α-突触核蛋白毒性、α-突触核蛋白介导的疾病或α-突触核蛋白纤维是疾病症状或病因的疾病中的一个或多个症状。在一种实施例中,用于组合物和方法的化合物是杂环基酰基胍、杂环基腙、二氢吡啶酮、杂环基和芳基苯乙酮以及杂环基吡唑。
  • Compounds, compositions and methods of inhibiting a-synuclein toxicity
    申请人:The Whitehead Institute for Biomedical Research
    公开号:EP2433634A2
    公开(公告)日:2012-03-28
    Compounds and compositions are provided for treatment or amelioration of one or more symptoms of a-synuclein toxicity, a-synuclein mediated diseases or diseases in which a-synuclein fibrils are a symptom or cause of the disease. In one embodiment, the compounds for use in the compositions and methods are heteroaryl acylguanidines, heteroarylhydrazones, dihydropyridones, heteroaryl and aryl styryl ketones, and heteroarylpyrazoles.
    提供的化合物和组合物用于治疗或改善a-突触核蛋白毒性、a-突触核蛋白介导的疾病或a-突触核蛋白纤维是症状或病因的疾病的一种或多种症状。在一个实施方案中,用于组合物和方法的化合物是杂芳基酰基胍、杂芳基肼、二氢吡啶酮、杂芳基和芳基苯乙烯基酮以及杂芳基吡唑。
  • STRODS YA. A.; KAMPARE R. B.; LIELBRIEDIS I. EH.; NEJLAND O. YA., XIMIYA GETEROTSIKL. SOEDIN., 1977, HO 7, 973-976
    作者:STRODS YA. A.、 KAMPARE R. B.、 LIELBRIEDIS I. EH.、 NEJLAND O. YA.
    DOI:——
    日期:——
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