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9,10-二氢蒽 | 14314-91-1

9,10-二氢蒽结构式图片|14314-91-1结构式图片
9,10-二氢蒽
Anthracene,9,10-dihydro-, ion(1-)
14314-91-1
C14H12
180.24508
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:9,10-二氢蒽结构式
11940
名称和标识符
InChIKey WPDAVTSOEQEGMS-UHFFFAOYSA-N
Inchi InChI=1S/C14H12/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-8H,9-10H2
SMILES C1=CC=C2CC3=CC=CC=C3CC2=C1
别名信息
- 中文别名 -
  • 9,10-二氢蒽
- 英文别名 -
  • Anthracene,9,10-dihydro-, ion(1-)
  • 9,10-Dihydroanthraceneanion
  • 9,10-DIHYDRO-ANTHRACENE
  • 9,10-DIHYDROANTHRACENE
  • CS-0155867
  • BDBM50060852
  • 613-31-0
  • UNII-Z142C238GB
  • D89677
  • D0549
  • Anthracene, dihydro-
  • NSC-30805
  • 9,10-Dihydro-anthracene
  • DTXSID3075256
  • MFCD00001239
  • FT-0621599
  • LS-14273
  • AKOS004907975
  • 9,10-Dihydroanthracene, 97%
  • 14314-91-1
  • Anthracene, 9,10-dihydro-
  • Z142C238GB
  • NSC30805
  • Q15634096
  • NS00034645
  • NSC 30805
  • EINECS 210-336-1
  • InChI=1/C14H12/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-8H,9-10H
  • CHEMBL125337
  • AI3-09026
  • Anthracene,10-dihydro-
物化性质
计算特性
精确分子量 180.093900383g/mol
氢键供体数量 0
氢键受体数量 0
可旋转化学键数量 0
同位素质量 180.093900383g/mol
重原子数量 14
复杂度 154
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) 4.2
拓扑分子极性表面积 0Ų
相关文献
  • 1. 195. The reaction of anthracence with benzyl radicals
    A. L. J. Beckwith,William A. Waters J. Chem. Soc. 1957 1001
  • 2. Steric interactions in substituted cyclohexadienes. Part I. meso-substituted dihydroanthracenes : steric effects in the reactions of cis- and trans-isomers
    A. H. Beckett,B. A. Mulley J. Chem. Soc. 1955 4159
  • 3. 205. The crystal structure of 9 : 10-dihydroanthracene and 9 : 10-dihydro-1 : 2 : 5 : 6-dibenzanthracene
    John Iball J. Chem. Soc. 1938 1074
  • 4. CCCCXIII.—The structure of the benzene nucleus. Part V. Some meso-derivatives of anthracene
    Christopher Kelk Ingold,Philip Guy Marshall J. Chem. Soc. 1926 129 3080
  • 5. Proton magnetic resonance of some 9,10-dihydroanthracenes
    W. Carruthers,G. E. Hall J. Chem. Soc. B 1966 861
  • 6. Intramolecular aldol-type condensation between side chains of naphthoquinones: biomimetic synthesis of 1,6- and 1,8-dihydroxyanthraquinones
    Hidemitsu Uno,Akane Masumoto,Erina Honda,Yumi Nagamachi,Youtarou Yamaoka,Noboru Ono J. Chem. Soc. Perkin Trans. 1 2001 3189
  • 7. 5. Polycyclic aromatic hydrocarbons. Part XXVII
    G. M. Badger,F. Goulden,F. Ll. Warren J. Chem. Soc. 1941 18
  • 8. Acidity of dibasic acids I: the second acidity constant of 9,10-dihydroanthracene and its 9,10-substituted derivatives: effect of substituent and counter ion
    Israel O. Shapiro,Malka Nir,Roy E. Hoffman,Mordecai Rabinovitz J. Chem. Soc. Perkin Trans. 2 1994 1519
  • 9. CCXIX.—The reactivity of meso-substituted anthracenes. Part II
    James Wilfred Cook J. Chem. Soc. 1926 129 1677
  • 10. LXXV.—The synthesis of meso-alkyl and meso-aryl anthracene derivatives. Part I
    Edward de Barry Barnett,James Wilfred Cook,Ivor Gray Nixon J. Chem. Soc. 1927 504
专业数据库参考
PubChemId 11940
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