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2-(5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl)phenol is a complex organic compound characterized by a phenol group attached to a 1,3,4-thiadiazol-2-yl moiety, which in turn is connected to a 4-methoxyphenyl group. This molecule features a sulfur atom in a five-membered ring, contributing to its unique chemical properties. The presence of the methoxy group on the phenyl ring provides additional functionality and potential for further chemical reactions. 2-(5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl)phenol may have applications in the fields of pharmaceuticals, agrochemicals, or as a building block in the synthesis of more complex molecules, due to its diverse functional groups and potential for interaction with biological targets.

4291-17-2

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4291-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4291-17-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4291-17:
(6*4)+(5*2)+(4*9)+(3*1)+(2*1)+(1*7)=82
82 % 10 = 2
So 4291-17-2 is a valid CAS Registry Number.

4291-17-2Downstream Products

4291-17-2Relevant academic research and scientific papers

2,5-Disubstituted thiadiazoles as potent β-glucuronidase inhibitors; Synthesis, in vitro and in silico studies

Taha, Muhammad,Barak Almandil, Noor,Rashid, Umer,Ali, Muhammad,Ibrahim, Mohamed,Gollapalli, Mohammed,Mosaddik, Ashik,Mohammed Khan, Khalid

, (2019/07/31)

Twenty-five thiadiazole derivatives 1–25 were synthesized from methyl 4-methoxybenzoate via hydrazide and thio-hydrazide intermediates, and evaluated for their potential against β-glucuronidase enzyme. Most of the compounds including 1 (IC50 = 26.05 ± 0.60 μM), 2 (IC50 = 42.53 ± 0.80 μM), 4 (IC50 = 38.74 ± 0.70 μM), 5 (IC50 = 9.30 ± 0.29 μM), 6 (IC50 = 6.74 ± 0.26 μM), 7 (IC50 = 18.40 ± 0.66 μM), and 15 (IC50 = 18.10 ± 0.53 μM) exhibited superior activity potential than the standard D-saccharic acid-1,4-lactone (IC50 = 48.4 ± 1.25 μM). Molecular docking studies were conducted to correlate the in vitro results and to identify possible mode of interaction with enzyme active site.

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