1961-97-3 (3-苯基-1H-茚,1H-Indene, 3-phenyl-)

快速询单

结构式：

3-苯基-1H-茚MOL文件

CAS号：

1961-97-3

中文名称：

3-苯基-1H-茚

英文名称：

1H-Indene, 3-phenyl-

分子式：

C₁₅H₁₂

分子量：

192.255784034729

3-苯基-1H-茚(1961-97-3)名称与标识符

名称

中文别名：

3-苯基-1H-茚;

英文别名：

1H-Indene, 3-phenyl-;3-phenyl-1H-Indene;1H-Indene,3-phenyl;1-phenylind-1-ene;1-Phenylindene;3-phenyl-1H-inden;3-phenyl-1-indene;3-Phenylinden;3-Phenylindene;DTXSID00293894;NSC-92814;ILASZRLOZFHWOJ-UHFFFAOYSA-N;A813894;NSC92814;1961-97-3;NSC 92814;AKOS004907971;FT-0706260;

标识符

InChIKey：

ILASZRLOZFHWOJ-UHFFFAOYSA-N

Inchi：

1S/C15H12/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)15/h1-9,11H,10H2

SMILES：

C12C=CC=CC=1CC=C2C1C=CC=CC=1

3-苯基-1H-茚(1961-97-3)物化性质

实验特性

LogP : 3.67440
PSA : 0.00000
折射率 : 1.637
沸点 : 313.6°C at 760 mmHg
闪点 : 148.6°C
密度 : 1.104

计算特性

精确分子量 : 192.09400
氢键供体数量 : 0
氢键受体数量 : 0
可旋转化学键数量 : 1
同位素质量 : 192.094
重原子数量 : 15
复杂度 : 245
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） : 3.9
拓扑分子极性表面积 : 0Å²

3-苯基-1H-茚(1961-97-3)上下游

苯基异喹啉

3-苯基-1H-茚(1961-97-3)相关文献

1. Acid-promoted cyclization of 2,4-diaryl-1,1,1-trifluorobut-3-en-2-oles and their TMS-ethers into CF3-indenes
Matvei Yu. Martynov,Roman O. Iakovenko,Anna N. Kazakova,Irina A. Boyarskaya,Aleksander V. Vasilyev Org. Biomol. Chem. 2017 15 2541
2. A click chemistry-based “grafting through” approach to the synthesis of a biorelevant polymer brush
A. Cappelli,M. Paolino,G. Grisci,G. Giuliani,A. Donati,R. Mendichi,A. C. Boccia,F. Samperi,S. Battiato,E. Paccagnini,E. Giacomello,V. Sorrentino,M. Licciardi,G. Giammona,S. Vomero Polym. Chem. 2011 2 2518
3. Hyaluronan-coated polybenzofulvene brushes as biomimetic materials
Andrea Cappelli,Marco Paolino,Giorgio Grisci,Vincenzo Razzano,Germano Giuliani,Alessandro Donati,Claudia Bonechi,Raniero Mendichi,Salvatore Battiato,Filippo Samperi,Cinzia Scialabba,Gaetano Giammona,Francesco Makovec,Mariano Licciardi Polym. Chem. 2016 7 6529
4. Nitrogen atom insertion into indenes to access isoquinolines
Patrick Finkelstein,Julia C. Reisenbauer,Bence B. Botlik,Ori Green,Andri Florin,Bill Morandi Chem. Sci. 2023 14 2954
5. Vinyl cations in organic synthesis. Part 2. A novel synthesis of methylene-1H-indenes (benzofulvenes) by cyclisation of phenyl-substituted but-1-en-3-ynes
Franco Marcuzzi,Ugo Azzena,Giovanni Melloni J. Chem. Soc. Perkin Trans. 1 1993 2957
6. Side chain engineering in π-stacked polybenzofulvene derivatives bearing electron-rich chromophores for OLED applications
Andrea Cappelli,Vincenzo Razzano,Giuseppe Fabio,Marco Paolino,Giorgio Grisci,Germano Giuliani,Alessandro Donati,Raniero Mendichi,Wojciech Mróz,Francesca Villafiorita-Monteleone,Chiara Botta RSC Adv. 2015 5 101377
7. The reaction of phenylmagnesium bromide with 2-benzoyl-1-indanone and its enol methyl ether
D. Auld,H. G. Heller J. Chem. Soc. C 1967 680
8. Spectroscopic studies on carbonium ions derived from aromatic olefins. Part III. Ions derived from styrene and cognate compounds
V. Bertoli,P. H. Plesch J. Chem. Soc. B 1968 1500
9. Palladium-catalyzed synthesis of indene derivatives via propargylic carbonates with in situ generated organozinc compounds
Zheng-Hui Guan,Zhi-Hui Ren,Lian-Biao Zhao,Yong-Min Liang Org. Biomol. Chem. 2008 6 1040
10. Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[a]azulenes
Maxime Giardinetti,Nicolaj Inunnguaq Jessen,Mette Louise Christensen,Karl Anker J?rgensen Chem. Commun. 2019 55 202