58755-07-0 Usage
Uses
Used in Pharmaceutical Applications:
(5E)-2-phenyl-5-(phenylmethylidene)[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one is used as a potential candidate in the pharmaceutical industry due to its diverse structural features and potential for biological activity. (5E)-2-phenyl-5-(phenylmethylidene)[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one's aromatic rings and heterocyclic moieties may allow it to interact with various biological targets, making it a promising molecule for the development of new drugs.
Used in Materials Science:
In the field of materials science, (5E)-2-phenyl-5-(phenylmethylidene)[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one may be utilized for the development of novel materials with specific properties. (5E)-2-phenyl-5-(phenylmethylidene)[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one's structural characteristics and potential chemical reactivity could contribute to the creation of advanced materials with applications in various industries.
Used in Organic Synthesis:
(5E)-2-phenyl-5-(phenylmethylidene)[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one can be employed as a key intermediate or building block in organic synthesis. Its unique structure and potential reactivity make it a valuable component for the synthesis of more complex molecules with specific functions or properties.
Check Digit Verification of cas no
The CAS Registry Mumber 58755-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,5 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58755-07:
(7*5)+(6*8)+(5*7)+(4*5)+(3*5)+(2*0)+(1*7)=160
160 % 10 = 0
So 58755-07-0 is a valid CAS Registry Number.
58755-07-0Relevant academic research and scientific papers
Synthesis and evaluation of anti-inflammatory activity of some thiazolo[3,2-b]-1,2,4-triazole-5(6H)-ones and their Michael addition products
Tozkoparan, Birsen,Kilcigil, Guelguen Ayhan,Ertan, Rahmiye,Ertan, Mevluet,Kelicen, Pelin,Demirdamar, Ruemeysa
, p. 1006 - 1011 (2007/10/03)
Thiazolo[3,2-b]-1,2,4-triazole-5(6H)-ones (4-10) were obtained in a one step synthesis by heating 3-aryl-5-mercapto-1,2,4-triazoles (3a-d) with chloroacetic acid and appropriate aromatic aldehyde in acetic acid and acetic anhydride in the presence of anhydrous NaOAc. Michael type addition of cyclic secondary amines (N-methylpiperazine, piperidine) to 4-10 gave 2-phenyl-6- (α-aminoarylmethyl)thiazolo[3,2-b]-1,2,4-triazole-5-ols (4a-10b). The structures of the compounds were confirmed by spectral and elementary analysis. The compounds synthesized in previous and present studies were investigated for their anti-inflammatory activities.
Fused Thiazoles: Synthesis and Antifungal Activity of 2-Arylidenethiazoloimidazopyridin-3(2H)-ones, 2-Arylidenethiazolobenzimidazol-3(2H)-ones and 6-Arylidenethiazolo-s-triazol-5(6H)-ones
Prasad, A. R.,Rao, A. Narasimha,Ramalingam, T.,Sattur, P. B.
, p. 776 - 778 (2007/10/02)
One-pot synthesis of the title compounds (II, IV) starting from 2-mercapto-1H-imidazopyridines (I; X=N), 2-mercaptobenzimidazoles (I; X=CH) or 5-aryl-3-mercapto-1,2,4-triazoles (III) is described.These compounds have been screened for their antifungal activities.
