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3-amino-2-hydrazinyl-5-phenyl-6-(phenylazo)thieno[2,3-d]pyrimidin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1325222-75-0

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1325222-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1325222-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,5,2,2 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1325222-75:
(9*1)+(8*3)+(7*2)+(6*5)+(5*2)+(4*2)+(3*2)+(2*7)+(1*5)=120
120 % 10 = 0
So 1325222-75-0 is a valid CAS Registry Number.

1325222-75-0Relevant academic research and scientific papers

Novel phenylazo derivatives of condensed and uncondensed thiophene. Synthesis, characterization, and antimicrobial studies

Gaber, Hatem M.,Bagley, Mark C.,Sherif, Sherif M.,Sayed, Mohsen A.

, p. 585 - 596 (2011/08/05)

In the search for new therapeutic agents against microbial infections, two novel series of monocyclic and tricyclic 5-(phenylazo)thiophene systems were synthesized based on 3-amino-2-thioxopyrimidinone and 2-cyanoacetamidothiophene derivatives 4 and 6. Functionalization of the pyrimidine ring in precursor 4 resulted in the formation of the target tricyclic condensed thiophenes 7, 12, and 13a, b, by the application of a variety of addition, substitution, and condensation reactions. On the other hand, derivatization of the versatile cyanoacetylated compound 6 led to a second series of monocyclic N-substituted aminothiophenes 15, 17, 19, and 20, through convenient methods. The new thiophene-based derivatives were tested for their antimicrobial activity with reference to relevant standard drugs. They displayed different levels of antibacterial activity, with compound 7 showing essentially the highest antipseudomonal activity. As for antifungal action, the compounds under investigation, unfortunately, had no inhibitory effects against test fungi isolates except for 7 and 20, that revealed slight inhibition.

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