19264-66-5 ((9H-carbazol-3-ylphenyl-Methanone)

快速询单

结构式：

9H-carbazol-3-ylphenyl-MethanoneMOL文件

CAS号：

19264-66-5

英文名称：

9H-carbazol-3-ylphenyl-Methanone

分子式：

C₁₉H₁₃NO

分子量：

271.312624692917

9H-carbazol-3-ylphenyl-Methanone(19264-66-5)名称与标识符

名称

英文别名：

9H-carbazol-3-ylphenyl-Methanone;9H-carbazol-3-yl(phenyl)methanone;3-Benzoyl-carbazol;3-benzoylcarbazole;9H-carbazol-3-yl-phenylmethanone;carbazol-3-yl-phenyl ketone;Carbazol-3-yl-phenyl-keton;KRVWAQOVNROOGA-UHFFFAOYSA;Methanone,9H-carbazol-3-ylphenyl;Methanone, 9H-carbazol-3-ylphenyl-;KRVWAQOVNROOGA-UHFFFAOYSA-;19264-66-5;SCHEMBL11069044;DTXSID70386166;(9H-Carbazol-3-yl)(phenyl)methanone;Oprea1_831729;CBMicro_049210;InChI=1/C19H13NO/c21-19(13-6-2-1-3-7-13)14-10-11-18-16(12-14)15-8-4-5-9-17(15)20-18/h1-12,20H;BIM-0049084.P001;

标识符

InChIKey：

KRVWAQOVNROOGA-UHFFFAOYSA-N

Inchi：

1S/C19H13NO/c21-19(13-6-2-1-3-7-13)14-10-11-18-16(12-14)15-8-4-5-9-17(15)20-18/h1-12,20H

SMILES：

O=C(C1C=CC=CC=1)C1C=CC2=C(C=1)C1C=CC=CC=1N2

9H-carbazol-3-ylphenyl-Methanone(19264-66-5)物化性质

实验特性

LogP : 4.55210
PSA : 32.86000

计算特性

精确分子量 : 271.10000
氢键供体数量 : 1
氢键受体数量 : 1
可旋转化学键数量 : 2
同位素质量 : 271.099714038g/mol
重原子数量 : 21
复杂度 : 387
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） : 5.1
拓扑分子极性表面积 : 32.9Å²

9H-carbazol-3-ylphenyl-Methanone(19264-66-5)上下游

9-苯甲酰卡唑咔唑苯甲酰氯

9H-carbazol-3-ylphenyl-Methanone(19264-66-5)相关文献

1. Synthesis, and the optical and electrochemical properties of a series of push–pull dyes based on the 4-(9-ethyl-9H-carbazol-3-yl)-4-phenylbuta-1,3-dienyl donor
Corentin Pigot,Guillaume Noirbent,Thanh-Tuan Bui,Sébastien Péralta,Sylvain Duval,Didier Gigmes,Malek Nechab,Frédéric Dumur New J. Chem. 2021 45 5808
2. Synthesis, aggregation-induced emission and electroluminescence properties of three new phenylethylene derivatives comprising carbazole and (dimesitylboranyl)phenyl groups
Heping Shi,Xinlei Zhang,Chen Gui,Shujuan Wang,Li Fang,Zujin Zhao,Shuming Chen,Ben Zhong Tang J. Mater. Chem. C 2017 5 11741
3. Competition between ultralong organic phosphorescence and thermally activated delayed fluorescence in dichloro derivatives of 9-benzoylcarbazole
Amir Sidat,Federico J. Hernández,Ljiljana Stojanovi?,Alston J. Misquitta,Rachel Crespo-Otero Phys. Chem. Chem. Phys. 2022 24 29437
4. TFAA/H3PO4 mediated unprecedented N-acylation of carbazoles leading to small molecules possessing anti-proliferative activities against cancer cells
Sunder Kumar Kolli,Bagineni Prasad,P. Vijaya Babu,Mohd Ashraf Ashfaq,Nasreen Z. Ehtesham,R. Ramesh Raju,Manojit Pal Org. Biomol. Chem. 2014 12 6080

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