7372-87-4 (1,8-二甲基菲,1,8-Dimethylphenanthrene)

快速询单

结构式：

1,8-二甲基菲MOL文件

CAS号：

7372-87-4

中文名称：

1,8-二甲基菲

英文名称：

1,8-Dimethylphenanthrene

分子式：

C₁₆H₁₄

分子量：

206.282364368439

1,8-二甲基菲(7372-87-4)名称与标识符

名称

中文别名：

1,8-二甲基菲;

英文别名：

1,8-Dimethylphenanthrene;1,8-Dimethylphenanthren;1,8-dimethyl-phenanthrene;1,8-Dimethylphenanthrene500µg;1,8-Dimethylphenantren;Phenanthrene,1,8-dimethyl;RM0Z9BR6MF;UNII-RM0Z9BR6MF;FT-0721049;LPHQUKCANLSJRU-UHFFFAOYSA-N;DTXSID90224031;7372-87-4;3-(3-ETHOXY-4-PROPOXY-PHENYL)-ACRYLICACID;Phenanthrene, 1,8-dimethyl-;DTXCID90146522;

标识符

InChIKey：

LPHQUKCANLSJRU-UHFFFAOYSA-N

Inchi：

1S/C16H14/c1-11-5-3-7-15-13(11)9-10-14-12(2)6-4-8-16(14)15/h3-10H,1-2H3

SMILES：

C12=CC=CC(C)=C1C=CC1C(C)=CC=CC2=1

1,8-二甲基菲(7372-87-4)物化性质

实验特性

LogP : 4.60980
PSA : 0.00000

计算特性

精确分子量 : 206.11000
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 : 206.109550447g/mol
重原子数量 : 16
复杂度 : 218
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） : 5.6
拓扑分子极性表面积 : 0Å²

1,8-二甲基菲(7372-87-4)推荐厂家更多厂家(1)

公司名称	手机号/电话	联系人	QQ	微信	询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695		询单

1,8-二甲基菲(7372-87-4)相关文献

1. The synthesis of alkylphenanthrenes relevant to the investigations on methyl vinhaticoate
F. E. King,T. J. King J. Chem. Soc. 1954 1373
2. 848. The chemistry of extractives from hardwoods. Part XV. The constitution of methyl vinhaticoate
F. E. King,T. J. King J. Chem. Soc. 1953 4158
3. 106. Synthesis of alkylphenanthrenes. Part VI. Attempts to synthesise the hydrocarbon “C16H14'” derived from strophanthidin
Robert Downs Haworth,Cecil Robert Mavin,George Sheldrick J. Chem. Soc. 1934 454
4. 296. Studies on the Diels–Alder reaction. Part II. The reaction between methylvinylcyclohexene and benzoquinone
P. A. Robins,James Walker J. Chem. Soc. 1952 1610
5. 71. Synthesis of polycyclic compounds. Part I. A new synthesis of alkylphenanthrenes
J. C. Bardhan,D. Nasipuri J. Chem. Soc. 1956 350
6. Notes
Alexander Mackie,Anand L. Misra,W. S. Fyfe,Duncan Taylor,J. C. Brunton,H. Suschitzky,Frank S. H. Head,C. W. Davies,B. E. Hoyle,G. A. Swan,H. O. Pritchard,F. H. Sumner,J. M. Anderson,Elizabeth Percival,T. H. Bevan,T. Malkin,D. B. Smith,L. G. Humber,W. I. Taylor J. Chem. Soc. 1955 1030
7. 229. Reduced cyclic compounds. Part III. The preparation and cyclodehydration of some unsaturated tertiary alcohols
M. F. Ansell,M. E. Selleck J. Chem. Soc. 1958 1167
8. 691. A proof of the constitution of cassanic acid based on its derivation from vouacapenic acid
F. E. King,T. J. King,J. M. Uprichard J. Chem. Soc. 1958 3428
9. 47. The constituents of high-boiling petroleum distillates. Part IV. Some polycyclic aromatic hydrocarbons in a Kuwait oil
W. Carruthers,A. G. Douglas J. Chem. Soc. 1957 278
10. A comparative study of two factor analytic models applied to PAH data from inhalable air particulate collected in an urban-industrial environment
Uwayemi M. Sofowote,Laurie M. Allan,Brian E. McCarry J. Environ. Monit. 2010 12 425