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1-methyl-4-nitro-5-[4-acetamido(phenylsulfonyl)]-1H-imidazole is a complex organic compound with the molecular formula C15H14N4O5S. It is a derivative of imidazole, a heterocyclic aromatic organic compound, and features a methyl group at the 1-position, a nitro group at the 4-position, and a 4-acetamido(phenylsulfonyl) group at the 5-position. 1-methyl-4-nitro-5-[4-acetamido(phenylsulfonyl)]-1H-imidazole is characterized by its unique structure, which includes a phenyl ring connected to a sulfonyl group, which in turn is linked to an acetamido group. The presence of these functional groups gives the compound specific chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's structure and properties make it a subject of interest for scientists studying the synthesis and reactivity of complex organic molecules.

5702-78-3

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5702-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5702-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5702-78:
(6*5)+(5*7)+(4*0)+(3*2)+(2*7)+(1*8)=93
93 % 10 = 3
So 5702-78-3 is a valid CAS Registry Number.

5702-78-3Downstream Products

5702-78-3Relevant academic research and scientific papers

Synthesis and In-vitro antibacterial activity of 5-substituted 1-methyl-4-nitro-1H-imidazoles

Letafat, Bahram,Emami, Saeed,Aliabadi, Alireza,Mohammadhosseini, Negar,Moshafi, Mohammad Hassan,Asadipour, Ali,Shafiee, Abbas,Foroumadi, Alireza

experimental part, p. 497 - 501 (2009/04/04)

A series of 5-substituted 1-methyl-4-nitro-1H-imidazole derivatives were synthesized and evaluated for in-vitro antibacterial activity against a panel of microorganisms including Staphylococcus aureus, Staphylococcus epidermidis, Bacillus subtilis, Esherichia coli, Klebsiella pneumonia, Entrobacter aerogenes, and Helicobacter pylori using conventional agar dilution method. Among the test compounds, 1-methyl-4-nitro-5-(phenylsulfonyl)-1H-imidazole was the most potent against Gram-positive bacteria, with a MIC value of ≤8 μg/mL. All compounds showed no significant activity against Gram-negative bacteria at concentrations ≤64 μg/mL The MIC values against 15 clinical isolates of H. pylori indicated that compounds 10 and 11 were the most active compounds in this series in terms of inhibiting the growth of H. pylori (MIC = 2 μg/mL). It was also demonstrated that their corresponding activities were four times larger than that of metronidazole.

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