317-17-9化工百科 – 960化工网

结构式：

吡咯并[1,2-a]喹啉MOL文件

CAS号：

317-17-9

中文名称：

吡咯并[1,2-a]喹啉

英文名称：

Pyrrolo[1,2-a]quinoline

分子式：

C₁₂H₉N

分子量：

167.206562757492

吡咯并[1,2-a]喹啉(317-17-9)名称与标识符

名称

英文别名：

Pyrrolo[1,2-a]quinoline;SCHEMBL1958088;XLIQPEZVRBALDD-UHFFFAOYSA-;10H-pyrrolo[1,2-a]quinoline;317-17-9;InChI=1/C12H9N/c1-2-6-12-10(4-1)7-8-11-5-3-9-13(11)12/h1-9H;DTXSID60446748;

标识符

InChIKey：

XLIQPEZVRBALDD-UHFFFAOYSA-N

Inchi：

1S/C12H9N/c1-2-6-12-10(4-1)7-8-11-5-3-9-13(11)12/h1-9H

SMILES：

N12C=CC=C1C=CC1C=CC=CC2=1

吡咯并[1,2-a]喹啉(317-17-9)物化性质

计算特性

精确分子量 : 167.073499291g/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 : 167.073499291g/mol
重原子数量 : 13
复杂度 : 190
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） : 3.8
拓扑分子极性表面积 : 4.4Å²

吡咯并[1,2-a]喹啉(317-17-9)相关文献

1. Facile synthesis of spiro[indoline-3,3′-pyrrolo[1,2-a]quinolines] and spiro[indoline-3,1′-pyrrolo[2,1-a]isoquinolines] via 1,3-dipolar cycloaddition reactions of heteroaromatic ammonium salts with 3-phenacylideneoxindoles
Lei Wu,Jing Sun,Chao-Guo Yan Org. Biomol. Chem. 2012 10 9452
2. Microwave assisted one pot three component synthesis of propargylamine, tetra substituted propargylamine and pyrrolo[1,2-a]quinolines using CuNPs@ZnO–PTh as a heterogeneous catalyst
Akshara P. Shah,Anuj S. Sharma,Shilpa Jain,Navinchandra G Shimpi New J. Chem. 2018 42 8724
3. Cerium(iii)-catalyzed cascade cyclization: an efficient approach to functionalized pyrrolo[1,2-a]quinolines
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4. Gold-catalyzed [4+1]-annulation reactions between anthranils and 4-methoxy-1,2-dienyl-5-ynes involving a 1,2-allene shift
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5. Synthesis of pyrrolo[1,2-a]quinolines and ullazines by visible light mediated one- and twofold annulation of N-arylpyrroles with arylalkynes
Amrita Das,Indrajit Ghosh,Burkhard K?nig Chem. Commun. 2016 52 8695
6. l-Proline derived nitrogenous steroidal systems: an asymmetric approach to 14-azasteroids
Ritesh Singh,Gautam Panda RSC Adv. 2013 3 19533
7. Copper NPs supported on hematite as magnetically recoverable nanocatalysts for a one-pot synthesis of aminoindolizines and pyrrolo[1,2-a]quinolines
U. Chinna Rajesh,V. Satya Pavan,Diwan S. Rawat RSC Adv. 2016 6 2935
8. Construction of benzo-fused indolizines, pyrrolo[1,2-a]quinolines via alkyne–carbonyl metathesis
Maloy Nayak,Ikyon Kim Org. Biomol. Chem. 2015 13 9697
9. Generation of 4-polyfluoroaryl pyrrolo[1,2-a]quinolines via C–H bond activation
Shengqing Ye,Jianping Liu,Jie Wu Chem. Commun. 2012 48 5028
10. A one-pot multicomponent strategy for stereospecific construction of tricyclic pyrrolo[1,2-a]quinolines
Tuan-Jie Li,Hong-Mei Yin,Chang-Sheng Yao,Xiang-Shan Wang,Bo Jiang,Shu-Jiang Tu,Guigen Li Chem. Commun. 2012 48 11966

317-17-9 (吡咯并[1,2-a]喹啉,Pyrrolo[1,2-a]quinoline)

吡咯并[1,2-a]喹啉(317-17-9)名称与标识符

名称

标识符

吡咯并[1,2-a]喹啉(317-17-9)物化性质

计算特性

吡咯并[1,2-a]喹啉(317-17-9)相关文献

目录