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(5E)-5-(4-methoxybenzylidene)-2-phenyl[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one is a complex organic compound characterized by the presence of a thiazole and triazole ring system, along with a benzylidene group and a methoxy substituent. Its unique structural features suggest potential pharmaceutical importance and the possibility of exhibiting various biological activities.

58755-08-1

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58755-08-1 Usage

Uses

Used in Pharmaceutical Industry:
(5E)-5-(4-methoxybenzylidene)-2-phenyl[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one is used as a potential candidate for the development of new drugs due to its unique structural features and potential biological activities. It may be utilized in the treatment of various diseases and conditions, pending further research and studies to fully understand and harness its potential in medicine and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 58755-08-1 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 58755-08:
(7*5)+(6*8)+(5*7)+(4*5)+(3*5)+(2*0)+(1*8)=161
161 % 10 = 1
So 58755-08-1 is a valid CAS Registry Number.

58755-08-1Downstream Products

58755-08-1Relevant 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.

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