5418-79-1 Usage
Member of the dihydroquinoline family
Indicates that the compound belongs to a specific group of chemical substances, sharing a common structure and properties with other members of this family.
Methyl group at the 1-position
A methyl (-CH3) functional group is attached to the first position of the quinoline ring, which influences the compound's chemical reactivity and properties.
2-(4-nitrophenyl)ethenyl group at the 2-position
A 2-(4-nitrophenyl)ethenyl functional group is attached to the second position of the quinoline ring, which contributes to the compound's unique structure and potential biological activities.
Trans configuration
The 2-(4-nitrophenyl)ethenyl group is in a trans configuration, meaning it is positioned opposite to the methyl group on the quinoline ring. This arrangement affects the compound's geometry, polarity, and interactions with other molecules.
Potential applications in medicinal chemistry and pharmaceutical research
The compound's unique structure may lead to interesting biological activities, making it a candidate for further study in drug development and understanding its potential therapeutic uses.
Need for further research and testing
The compound's potential uses and effects are not yet fully understood, and additional studies are required to explore its properties and possible applications in the field of medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 5418-79-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5418-79:
(6*5)+(5*4)+(4*1)+(3*8)+(2*7)+(1*9)=101
101 % 10 = 1
So 5418-79-1 is a valid CAS Registry Number.
5418-79-1Relevant academic research and scientific papers
Design and Synthesis of Novel c-di-GMP G-Quadruplex Inducers as Bacterial Biofilm Inhibitors
Chen, Wei-Min,Lin, Jing,Lin, Qian-Wen,Liu, Jun,Wang, Zi-Qiang,Xuan, Teng-Fei,Yu, Hai-Tao
, p. 11074 - 11089 (2021/08/20)
The formation of biofilms by clinical pathogens typically leads to chronic and recurring antibiotic-resistant infections. High cellular levels of cyclic diguanylate (c-di-GMP), a ubiquitous secondary messenger of bacteria, have been proven to be associate
Synthesis, spectroscopy and computational studies of some novel π-conjugated vinyl N-alkylated quinolinium salts and their precursor's
Nycz, Jacek E.,Czyz, Karolina,Szala, Marcin,Malecki, Jan G.,Shaw, George,Gilmore, Brendan,Jon, Marek
, p. 416 - 423 (2015/11/27)
A series of π-conjugated vinyl N-methylated quinolinium salts (3) and their precursor's N-alkylated quinolinium salts (2) were prepared and characterized by NMR, IR, UV-Vis and MS spectroscopy. It was confirmed that the hydroxyl and amino derivatives of vinyl N-methylated quinolinium salts lead to spiro type compounds (4). The syntheses of N-alkylated quinolinium salts were successful, and even multigram scale was achievable. The structures of 1,2-dimethylquinolinium iodide (2a) and 1-ethyl-2-methylquinolinium iodide (2b) were determined by single crystal X-ray diffraction method. NMR spectra showed readily diagnostic H-1 and C-13 signals from methyl and N-alkyl groups for both 2 and 3. The geometries of the studied compounds were optimized in singlet states using the density functional theory (DFT) method with B3LYP functional. In general, the predicted bond lengths and angles are in a good agreement with the values based on the X-ray crystal structure data.
