46870-92-2 (6-methoxy-4-phenylquinoline,6-Methoxy-4-phenylquinoline)

快速询单

结构式：

6-methoxy-4-phenylquinolineMOL文件

CAS号：

46870-92-2

中文名称：

6-methoxy-4-phenylquinoline

英文名称：

6-Methoxy-4-phenylquinoline

分子式：

C₁₆H₁₃NO

分子量：

235.280524015427

6-methoxy-4-phenylquinoline(46870-92-2)名称与标识符

名称

中文别名：

6-methoxy-4-phenylquinoline;

英文别名：

46870-92-2;DTXSID50492779;DTXCID50443589;4-Phenyl-6-methoxyquinoline;6-Methoxy-4-phenylquinoline;

标识符

InChIKey：

KRQFONREMHZAAW-UHFFFAOYSA-N

Inchi：

1S/C16H13NO/c1-18-13-7-8-16-15(11-13)14(9-10-17-16)12-5-3-2-4-6-12/h2-11H,1H3

SMILES：

O(C)C1C=CC2C(C=1)=C(C=CN=2)C1C=CC=CC=1

6-methoxy-4-phenylquinoline(46870-92-2)物化性质

计算特性

精确分子量 : 235.099714038Da
氢键供体数量 : 0
氢键受体数量 : 2
可旋转化学键数量 : 2
同位素质量 : 235.099714038Da
重原子数量 : 18
复杂度 : 262
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 : 22.1Å²

6-methoxy-4-phenylquinoline(46870-92-2)相关文献

1. An environmentally benign regioselective synthesis of 2-benzyl-4-arylquinoline derivatives using aryl amines, styrene oxides and aryl acetylenes
Saghir Ali,Abu T. Khan Org. Biomol. Chem. 2021 19 8772
2. Visible-light-enabled aerobic oxidative Csp3–H functionalization of glycine derivatives using an organic photocatalyst: access to substituted quinoline-2-carboxylates
Jingxin Wang,Liqi Li,Ying Guo,Shengyu Li,Shutao Wang,Ying Li,Yuan Zhang Org. Biomol. Chem. 2020 18 8179
3. p-TSA·H2O catalyzed metal-free and environmentally benign synthesis of 4-aryl quinolines from arylamine, arylacetylene, and dimethyl sulfoxide
Simra Faraz,Abu Taleb Khan Org. Biomol. Chem. 2023 21 7553
4. Imidazoquinolinethiones from 8-aminoquinolines by a novel peri-participation
Thierry Besson,Charles W. Rees,David G. Roe,Valérie Thiéry J. Chem. Soc. Perkin Trans. 1 2000 555
5. Synthesis, and the antioxidant, neuroprotective and P-glycoprotein induction activity of 4-arylquinoline-2-carboxylates
Jaideep B. Bharate,Abubakar Wani,Sadhana Sharma,Shahi Imam Reja,Manoj Kumar,Ram A. Vishwakarma,Ajay Kumar,Sandip B. Bharate Org. Biomol. Chem. 2014 12 6267
6. An economical synthesis of substituted quinoline-2-carboxylates through the potassium persulfate-mediated cross-dehydrogenative coupling of N-aryl glycine derivatives with olefins
Guoliang Liu,Jiarui Qian,Jing Hua,Feng Cai,Xia Li,Lei Liu Org. Biomol. Chem. 2016 14 1147
7. AgNO3-catalyzed direct C–H arylation of quinolines by oxidative decarboxylation of aromatic carboxylic acids
Jin-Wei Yuan,Liang-Ru Yang,Pu Mao,Ling-Bo Qu Org. Chem. Front. 2017 4 545
8. Imidazoquinolinethiones from quinolines: a new molecular rearrangement
Charles W. Rees,David G. Roe,Valérie Thiéry Chem. Commun. 1996 2775

46870-92-2 (6-methoxy-4-phenylquinoline,6-Methoxy-4-phenylquinoline)

6-methoxy-4-phenylquinoline(46870-92-2)名称与标识符

名称

标识符

6-methoxy-4-phenylquinoline(46870-92-2)物化性质

计算特性

6-methoxy-4-phenylquinoline(46870-92-2)相关文献

目录