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3-乙酰基菲 | 2039-76-1

3-乙酰基菲
3-Acetylphenanthrene
2039-76-1
C16H12O
220.26588
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:3-乙酰基菲结构式
24890605
3-乙酰基菲价格
名称和标识符
MDL MFCD00001169
InChIKey JKVNPRNAHRHQDD-UHFFFAOYSA-N
Inchi InChI=1S/C16H12O/c1-11(17)14-9-8-13-7-6-12-4-2-3-5-15(12)16(13)10-14/h2-10H,1H3
SMILES CC(=O)C1=CC2=C(C=CC3=CC=CC=C32)C=C1
别名信息
- 中文别名 -
  • 3-乙酰基菲
  • 3-乙酰菲
- 英文别名 -
  • 1-(Phenanthren-3-yl)ethanone
  • 3-ACETYLPHENANTHRENE
  • 1-(3-Phenanthryl)ethanone
  • Ethanone, 1-(3-phenanthrenyl)-
  • Ketone, methyl 3-phenanthryl
  • methyl 3-phenanthryl ketone
  • 1-phenanthren-3-ylethanone
  • 1-(3-phenanthrenyl)-ethanone
  • 1-[3]Phenanthryl-aethanon
  • 1-[3]phenanthryl-ethanone
  • Ethanone,1-(3-phenanthrenyl)
物化性质
实验特性
LogP 4.19560
PSA 17.07000
熔点 67-71 °C (lit.)
颜色与性状 未确定
溶解性 未确定
计算特性
精确分子量 220.08900
氢键供体数量 0
氢键受体数量 1
可旋转化学键数量 1
重原子数量 17
复杂度 296
同位素原子数量 0
确定原子立构中心数量 0
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP) 4.1
互变异构体数量 2
表面电荷 0
国际标准相关数据
EINECS 218-020-5
海关数据
海关编码 2914399090
海关数据

中国海关编码:

2914399090

概述:

2914399090. 其他不含其他含氧基的芳香酮. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:5.5%. 普通关税:30.0%

申报要素:

品名, 成分含量, 用途, 丙酮报明包装

Summary:

2914399090. other aromatic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

相关文献
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  • 2. Visible-light excited red emitting luminescent nanocomposites derived from Eu3+-phenathrene-based fluorinated β-diketonate complexes and multi-walled carbon nanotubes
    V. Divya,M. L. P. Reddy J. Mater. Chem. C 2013 1 160
  • 3. Infrared study of the desorption of polycondensed aromatic compounds by non-ionic surfactants at the silica–carbon tetrachloride interface
    Yves Lijour,Jean-Yves Calves,Pierre Saumagne J. Chem. Soc. Faraday Trans. 1 1987 83 3295
  • 4. Amphiphilic properties of a polymerized glycolipid surfactant
    Bernard Boyer,Sylvie Durand,Gérard Lamaty,Jean Marie Moussamou-Missima,André A. Pavia,Bernard Pucci,Jean Pierre Roque,Jacques Rouvière J. Chem. Soc. Perkin Trans. 2 1991 1311
  • 5. Carcinogenic nitrogen compounds. Part XVI. Some condensed carbazoles and their thiophen analogues
    Ng. Ph. Buu-Ho?,P. Jacquignon J. Chem. Soc. 1954 513
  • 6. Notes
    C. C. Addison,N. Hodge,R. Thompson,D. J. Bell,D. J. Manners,S. Bayne,Jennifer Wildy,W. Gerrard,W. J. Green,R. J. Phillips,D. G. Bew,G. R. Clemo,R. L. Werner,P. D. Lark,R. J. Bates,J. Cymerman-Craig,Wadie Tadros,Ezzat Saad,J. B. Harborne,A. S. Weaving,John Harley-Mason,A. H. Jackson,J. H. Barnes,P. G. Marshall,Morton Meadow,Wilson M. Whaley,J. D. Loudon,D. K. V. Steel J. Chem. Soc. 1954 1143
  • 7. 143. New thiosemicarbazones and 4-oxo-Δ2-thiazolin-2-ylhydrazones
    Ng. Ph. Buu-Ho?,Ng. D. Xuong,F. Binon J. Chem. Soc. 1956 713
  • 8. 105. Polycyclic aromatic hydrocarbons. Part XVII. Completion of the synthesis of the twelve monomethyl-1 : 2-benzanthracenes
    J. W. Cook,A. M. Robinson J. Chem. Soc. 1938 505
  • 9. The friedel–crafts acetylation of phenanthrene
    R. B. Girdler,P. H. Gore,C. K. Thadani J. Chem. Soc. C 1967 2619
  • 10. 1134. The kinetics and mechanisms of aromatic halogen substitution. Part XVII. Chlorination of 9,10-dihydrophenanthrene
    P. B. D. de la Mare,E. A. Johnson,J. S. Lomas J. Chem. Soc. 1963 5973
专业数据库参考
PubChemId 24890605
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