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2H-1,2,3-Triazole-4,5-dicarboxamide(9CI) is a chemical compound belonging to the triazole family, characterized by the molecular formula C5H5N5O2. It is a derivative known for its potential applications in pharmaceutical and agricultural sectors, with ongoing research exploring its capabilities.

388623-87-8

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388623-87-8 Usage

Uses

Used in Pharmaceutical Applications:
2H-1,2,3-Triazole-4,5-dicarboxamide(9CI) is utilized as an antitumor agent for its potential to inhibit the growth of cancer cells. It has been studied for its effectiveness in combating various types of cancer, making it a promising candidate for further research and development in oncology.
Used in Agricultural Applications:
In the agricultural industry, 2H-1,2,3-Triazole-4,5-dicarboxamide(9CI) is employed as an antimicrobial agent. Its potential as a fungicide and bactericide has been investigated, with the aim of protecting crops from various microbial infections and diseases, thereby enhancing crop yield and quality.

Check Digit Verification of cas no

The CAS Registry Mumber 388623-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,8,6,2 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 388623-87:
(8*3)+(7*8)+(6*8)+(5*6)+(4*2)+(3*3)+(2*8)+(1*7)=198
198 % 10 = 8
So 388623-87-8 is a valid CAS Registry Number.

388623-87-8Downstream Products

388623-87-8Relevant academic research and scientific papers

Novel 2H-1,2,3-Triazole sodium complex from N-[2-amino-1,2-dicyanovinyl]alkanamides

AL-Azmi, Amal,George, Paulson,El-Dusouqui, Osman M.E.

, p. 2183 - 2201 (2008/09/17)

Diazotization at 0 °C of N-[2-amino-1,2-dicyanovinyl]ethanamide 2a or propanamide 2b prepared from diaminomaleonitrile (DAMN) 1 using aqueous acetic acid and NaNO2 solution furnished sodium complex 3. The X-ray structure of the complex 3 showed that it is a 1:1 mixture of the neutral 2H-triazole heterocycle 4ii and its anion deprotonated at the central (N) atom of the ring, together with a sodium counter ion and two coordinated water molecules. However, when the diazotization reaction was carried out in the presence of aqueous HCl, the product was 5-cyano-2H-[1,2,3]triazole-4-carboxylic acid amide monohydrate 4ii. Diazotization of DAMN 1 using aqueous HCl furnished 1H-1,2,3-triazole-4,5-dicarbonitrile 5, whereas with acetic acid there was no reaction, and hence no route analogous to that leading to complex 3. The structure of both complex 3 and the triazole monohydrate 4ii were solved using X-ray crystallography, and the compounds under study were fully characterized using spectroscopic techniques.

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