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4-methyl-2-phenyl-5-(2-phenylthiazol-4-yl)thiazole is a complex organic compound characterized by its unique molecular structure. It features a thiazole ring system, which is a five-membered heterocyclic ring containing sulfur and nitrogen atoms. The compound is further adorned with a methyl group at the 4-position, a phenyl group at the 2-position, and another phenylthiazol-4-yl group at the 5-position, which itself is a phenyl-substituted thiazole. This intricate arrangement of functional groups endows the molecule with specific chemical properties and potential applications in various fields, such as pharmaceuticals or materials science, where its stability, reactivity, and interaction with other molecules can be exploited.

7520-97-0

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7520-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7520-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7520-97:
(6*7)+(5*5)+(4*2)+(3*0)+(2*9)+(1*7)=100
100 % 10 = 0
So 7520-97-0 is a valid CAS Registry Number.

7520-97-0Downstream Products

7520-97-0Relevant academic research and scientific papers

Synthesis and biological screening of 2′-aryl/benzyl-2-aryl-4-methyl-4′,5-bithiazolyls as possible anti-tubercular and antimicrobial agents

Abhale, Yogita K.,Sasane, Amit V.,Chavan, Abhijit P.,Deshmukh, Keshav K.,Kotapalli, Sudha Sravanti,Ummanni, Ramesh,Sayyad, Sadikali F.,Mhaske, Pravin C.

, p. 340 - 347 (2015)

A series of 2′-aryl/benzyl-2-aryl-4-methyl-4′,5-bithiazolyl derivatives, 25-64 were synthesized and evaluated for inhibitory activity against Mycobacterium smegmatis MC2 155 strain and antimicrobial activities against four pathogenic bacteria Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Proteus vulgaris. Among them, compounds 40, 49, 50, and 54 exhibited moderate to good inhibition on the growth of the bacteria Mycobacterium smegmatis at the concentration of 30 μM. Compounds 26, 40, 44, 54 and 56 exhibited moderate to good antibacterial activity. Compound 5-(2′-(4-fluorobenzyl)thiazol-4′-yl)-2-(4-fluorophenyl)-4-methyl-thiazole (54) exhibited both antitubercular as well as antimicrobial activity against all tested strains.

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