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Ethyl 2-(4-nitrophenyl)-2H-tetrazole-5-carboxylate is a chemical compound with the molecular formula C10H10N4O4. It is a derivative of tetrazole, a heterocyclic compound with a five-membered ring containing four nitrogen atoms. This specific compound features a 4-nitrophenyl group attached to the tetrazole ring, and an ethyl ester group at the 5-position. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and ability to form stable complexes with metal ions. The compound is typically synthesized through the reaction of ethyl 5-aminotetrazole-2-carboxylate with 4-nitrobenzaldehyde, followed by cyclization. It is an important building block in the development of new drugs and chemical compounds, particularly those with potential applications in the fields of medicine and agriculture.

3654-53-3

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3654-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3654-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3654-53:
(6*3)+(5*6)+(4*5)+(3*4)+(2*5)+(1*3)=93
93 % 10 = 3
So 3654-53-3 is a valid CAS Registry Number.

3654-53-3Relevant academic research and scientific papers

Regioselective synthesis of carboxylic and fluoromethyl tetrazoles enabled by silver-catalyzed cycloaddition of diazoacetates and aryl diazonium salts

Xiao, Ming-Yang,Chen, Zhen,Zhang, Fa-Guang,Ma, Jun-An

supporting information, (2020/03/04)

Here we present a dipolar [3 + 2] cycloaddition transformation of diazoacetates with arenediazonium salts under silver catalysis, thus offering a straightforward approach for the regioselective construction of carboxylic tetrazoles. Several merits are accompanied with this reaction including readily available starting reagents, broad coupling scope, high yields, and friendly reaction conditions. The synthetic value is further showcased by one-pot conversion of commercially available primary arylamines to tetrazoles and successful transformations of the cycloadducts into valuable 5-fluoromethyltetrazoles and an analogue of P2X3 receptor antagonist.

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