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N-((1H-benzimidazol-2-yl)methyl)-4-phenylthiazol-2-amine is a complex organic compound with the molecular formula C18H14N4S. It is characterized by a benzimidazole ring attached to a thiazol-2-amine group through a methylene bridge. N-((1H-benzimidazol-2-yl)methyl)-4-phenylthiazol-2-amine is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. Its structure allows for the exploration of different pharmacological properties, making it a valuable compound in the development of new drugs. The specific applications and therapeutic potential of N-((1H-benzimidazol-2-yl)methyl)-4-phenylthiazol-2-amine are subject to ongoing research and may vary depending on the context of its use.

2211-39-4

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2211-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2211-39-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2211-39:
(6*2)+(5*2)+(4*1)+(3*1)+(2*3)+(1*9)=44
44 % 10 = 4
So 2211-39-4 is a valid CAS Registry Number.

2211-39-4Downstream Products

2211-39-4Relevant academic research and scientific papers

Synthesis, antibacterial, and anti HepG2 cell line human hepatocyte carcinoma activity of some new potentially benzimidazole-5-(aryldiazenyl)thiazole derivatives

Khalifa, Mohamed E.,Gobouri, Adil A.,Kabli, Fahad M.,Altalhi, Tarik A.,Almalki, Abdulraheem S.A.,Mohamed, Mahmoud A.

, (2018)

The paper describes the synthesis and biological evaluation of some new benzimidazole derivatives as potent clinical drugs that are useful in the treatment of some microbial infections and tumor inhibition. The starting compound 2-(bromomethyl)-1H-benzimidazole (1) was prepared, and hence underwent interesting functionalization reactions to afford several series of benzimidazole-5-(aryldiazenyl)thiazole derivatives: 3a–c, 7a–c, and 8a–c. The antibacterial activities of the synthesized compounds were evaluated by calculation of the inhibition zone diameter (mm) and the determination of minimum inhibitory concentration (μg/mL) against selected pathogenic bacteria Staphylococcus aureus (Gram-positive bacteria) and Escherichia coli (Gram-negative bacteria).Noticeable efficiency was found based on in vitro screening for their antioxidant activity and cytotoxicity effect against the human liver cancer cell line (HepG2) and human hepatocyte carcinoma cells at relatively high concentrations.

Synthesis and fungicidal activity of new imidazoles from 2-(chloromethyl)-1H-benzimidazole

Madkour,Farag,Ramses,Ibrahiem

, p. 255 - 265 (2007/10/03)

A series of substituted 2-thiomethylbenzimidazoles 2-4, 2-phenoxy-methylbenzimidazoles 5 and 2-aminomethylbenzimidazoles 6 and 7 were synthesized by reactions of 2-chloromethylbenzimidazole 1 with dithiocarbamate, pyrimidine-2-thiones, phenol derivatives,

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