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2-(4-fluorophenyl)-5-phenylthiazole is a chemical compound with the molecular formula C15H10FNS. It is a derivative of thiazole, a heterocyclic compound consisting of a five-membered ring with one sulfur atom and one nitrogen atom. The structure of 2-(4-fluorophenyl)-5-phenylthiazole features a 4-fluorophenyl group attached to the 2-position of the thiazole ring and a phenyl group at the 5-position. 2-(4-fluorophenyl)-5-phenylthiazole is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as in materials science. Its specific properties, such as solubility, stability, and reactivity, can be influenced by the presence of the fluorine atom, which can affect its electronic and steric characteristics. The compound is typically synthesized through various chemical reactions and can be used as a building block for more complex molecules.

1493-43-2

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1493-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1493-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1493-43:
(6*1)+(5*4)+(4*9)+(3*3)+(2*4)+(1*3)=82
82 % 10 = 2
So 1493-43-2 is a valid CAS Registry Number.

1493-43-2Downstream Products

1493-43-2Relevant academic research and scientific papers

Cu-Catalyzed Aerobic Oxidative Sulfuration/Annulation Approach to Thiazoles via Multiple Csp3-H Bond Cleavage

Wang, Xiaoyang,Qiu, Xu,Wei, Jialiang,Liu, Jianzhong,Song, Song,Wang, Wen,Jiao, Ning

supporting information, p. 2632 - 2636 (2018/05/22)

A novel and practical Cu-catalyzed aerobic oxidative synthesis of thiazoles was developed. This chemistry for the first time achieved thiazole construction from simple aldehydes, amines, and element sulfur through multiple Csp3-H bond cleavage processes. Molecular oxygen was used as a green oxidant in this oxidative protocol. The substrate scope is broad with the tolerance of aliphatic amines. The mechanistic study might promote the reaction design for a new sulfuration/annulation reaction with readily available element sulfur.

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