14314-91-1 (9,10-二氢蒽,Anthracene,9,10-dihydro-, ion(1-))

快速询单

结构式：

9,10-二氢蒽MOL文件

CAS号：

14314-91-1

中文名称：

9,10-二氢蒽

英文名称：

Anthracene,9,10-dihydro-, ion(1-)

分子式：

C₁₄H₁₂

分子量：

180.245083808899

9,10-二氢蒽(14314-91-1)名称与标识符

名称

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;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-;Anthracene, 9,10dihydro;DTXCID6042999;DB-242979;Anthracene, dihydro;210-336-1;dihydroanthracene;STK365298;

标识符

InChIKey：

WPDAVTSOEQEGMS-UHFFFAOYSA-N

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：

C1C2C=CC=CC=2CC2C=CC=CC1=2

9,10-二氢蒽(14314-91-1)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 : 0Å²

9,10-二氢蒽(14314-91-1)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