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The chemical compound "CH3C6H4NHNC(CN)C(CH3)NH" is a complex organic molecule with a molecular formula that can be interpreted as a derivative of aniline, where one hydrogen atom on the benzene ring is replaced by a methyl group (CH3), and the amino group (NH2) is replaced by a more complex structure. This structure includes a secondary amine (NH) connected to a benzene ring, which is further connected to a cyano group (CN) and a methyl group (CH3) on a nitrogen atom. The compound is characterized by its potential to form multiple hydrogen bonds due to the presence of both hydrogen-bond donor (NH) and acceptor (CN) groups. It is likely to have significant biological activity due to its complex structure and the presence of functional groups that can interact with biological targets.

5110-98-5

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5110-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5110-98-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5110-98:
(6*5)+(5*1)+(4*1)+(3*0)+(2*9)+(1*8)=65
65 % 10 = 5
So 5110-98-5 is a valid CAS Registry Number.

5110-98-5Downstream Products

5110-98-5Relevant academic research and scientific papers

Anticancer, antimicrobial, and DNA protection analysis of novel 2,4-dihydroxyquinoline dyes

?ener, Nesrin,Mohammed, Hassan Jaballah Abdullah,Yerlikaya, Serife,Celik Altunoglu, Yasemin,Gür, Mahmut,Baloglu, Mehmet Cengiz,?ener, ?zzet

, p. 11 - 19 (2018/05/04)

A new series of 2,4-dihydroxyquinoline derived disazo dyes has been synthesized by the reaction of 5-amino-4-phenylazo-3-methyl-1H-pyrazole derivatives with 2,4-dihydroxyquinoline. The structures of the obtained dyes were identified by various spectrophotometric methods such as FT-IR, 1H-NMR, and elemental analysis. The synthesized compounds were also examined for different biological activities, including DNA protection, antimicrobial, and anticancer activities. Compound 3b was found most effective on Gram-positive bacteria. A DNA protection assay was applied to all compounds, and it was found that compounds 3h and 3j had a high capacity for binding to DNA. Besides, compounds 3h and 3j showed cytotoxicity against HeLa and PC3 cancer cell lines. These compounds could potentially be used as drugs or drug additives based on their effects on bacterial and cancer cell lines.

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