14229-93-7 Usage
General Description
2,4-Diphenyl-5-methylthiazole is a chemical compound with the molecular formula C16H13NS. 2,4-DIPHENYL-5-METHYLTHIAZOLE is a thiazole derivative, which is a five-membered heterocyclic ring containing four carbon atoms, one sulfur atom, and one nitrogen atom. It is commonly used in organic synthesis and pharmaceutical research due to its potential biological and pharmacological properties. Its structural features make it useful for the development of new drugs and agrochemicals. Additionally, 2,4-diphenyl-5-methylthiazole has been studied for its potential antimicrobial, antifungal, and antioxidant activities, making it a valuable compound for various scientific and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 14229-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,2 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14229-93:
(7*1)+(6*4)+(5*2)+(4*2)+(3*9)+(2*9)+(1*3)=97
97 % 10 = 7
So 14229-93-7 is a valid CAS Registry Number.
14229-93-7Relevant articles and documents
Four-component thiazole formation from simple chemicals under metal-free conditions
Jiang, Jingjing,Huang, Huawen,Deng, Guo-Jun
supporting information, p. 986 - 990 (2019/03/12)
Multi-component reactions for the synthesis of polysubstituted thiazoles from simple chemicals are described. Under metal-free reaction conditions, cheap and easily available ketones, aldehydes, ammonium salt, and elemental sulfur are self-assembled to provide entries to three thiazoles in moderate to good yield with a range of functionalities tolerated.
One pot synthesis of substituted imidazopyridines and thiazoles from styrenes in water assisted by NBS
Shinde, Mahesh H.,Kshirsagar, Umesh A.
, p. 1455 - 1458 (2016/04/04)
Heating of commercially available styrenes with NBS in water followed by reaction with 2-aminopyridines or thioamides afforded important heterocyclic scaffolds in a one pot procedure. The reaction proceeds via co-oxidant free, in situ formation of α-bromoketone using NBS as a bromine source as well as an oxidant followed by trapping with suitable nucleophiles to provide imidazopyridines and thiazoles.
