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3-乙酰基-4-羟基-2-苯基喹啉 | 101600-64-0

中文名称
3-乙酰基-4-羟基-2-苯基喹啉
中文别名
——
英文名称
3-acetyl-4-hydroxy-2-phenylquinoline
英文别名
1-(4-hydroxy-2-phenyl-[3]quinolyl)-ethanone;1-(4-Hydroxy-2-phenyl-[3]chinolyl)-aethanon;Ethanone, 1-(4-hydroxy-2-phenyl-3-quinolinyl)-;3-acetyl-2-phenyl-1H-quinolin-4-one
3-乙酰基-4-羟基-2-苯基喹啉化学式
CAS
101600-64-0
化学式
C17H13NO2
mdl
——
分子量
263.296
InChiKey
JFRVNPXEGYNJDY-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:
    282-284 °C(Solv: acetic acid (64-19-7))
  • 沸点:
    457.3±45.0 °C(Predicted)
  • 密度:
    1.241±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    46.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    3-乙酰基-4-羟基-2-苯基喹啉 在 selenium(IV) oxide 、 乙醇 作用下, 生成 (4-hydroxy-2-phenyl-[3]quinolyl)-glyoxal
    参考文献:
    名称:
    Structures of the Products Obtained by the Condensation of Phenylbenzimino Chloride and Ethyl Sodioacetoacetate and Subsequent Cyclization1
    摘要:
    DOI:
    10.1021/ja01604a042
  • 作为产物:
    参考文献:
    名称:
    Structures of the Products Obtained by the Condensation of Phenylbenzimino Chloride and Ethyl Sodioacetoacetate and Subsequent Cyclization1
    摘要:
    DOI:
    10.1021/ja01604a042
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文献信息

  • Regioselective Condensation of Alkylidenephosphoranes with Bifunctionalized Compounds: New Approach to the Synthesis of Fused<i>O</i>- and<i>N</i>-Heterocycles
    作者:Wafaa M. Abdou、Neven A. F. Ganoub、Amin F. M. Fahmy、Abeer A. M. Shaddy
    DOI:10.1080/104265090921092
    日期:2005.10
    A series of fused pyran- (similar to 40% yield) and furan- (similar to 20% yield) derivatives were regioselectively prepared from the reactions of 5,6-difur-2'y1-3-oxo-2,3-dihydropyridazin-4-carbonitrile with ester- and keto phosphorus ylides, whereas new ylides were obtained, in addition to fused furans, in almost equal yields (33%) from the reaction of the same substrate with cyanomethylene(triphenyl)phosphorane. However application of such Wittig reagents on 2[(benzylidene)amino]-benzonitrile afforded, in all cases, 4-hydroxyquinalines in a similar to 42% yield as major products. Moreover; 2-[(triphenylphosphoranylidene)amino] benzonitrile, with the corresponding alkene, was also isolated a side products.
  • Sinsky, M. S.; Bass, R. G., Journal of Heterocyclic Chemistry, 1984, vol. 21, p. 759 - 768
    作者:Sinsky, M. S.、Bass, R. G.
    DOI:——
    日期:——
  • A New Synthesis of 2-Aryl-3-acetyl-4-hydroxyquinolines Using Polyphosphoric Acid
    作者:B. STASKUN
    DOI:10.1021/jo01066a040
    日期:1961.8
  • SINSKY, M. S.;BASS, R. G., J. HETEROCYCL. CHEM., 1984, 21, N 3, 759-768
    作者:SINSKY, M. S.、BASS, R. G.
    DOI:——
    日期:——
  • Structures of the Products Obtained by the Condensation of Phenylbenzimino Chloride and Ethyl Sodioacetoacetate and Subsequent Cyclization<sup>1</sup>
    作者:Gurbakhsh Singh、G. V. Nair
    DOI:10.1021/ja01604a042
    日期:1956.12
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