90418-58-9 Usage
Uses
Used in Pharmaceutical Industry:
Pyridin-2-yl(thiazol-2-yl)Methanone is used as a key intermediate in the synthesis of various bioactive molecules for therapeutic applications. Its unique structure allows for the development of new drugs with potential to treat a range of diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, pyridin-2-yl(thiazol-2-yl)Methanone is utilized as a building block for the creation of novel pesticides. Its chemical properties make it a valuable component in the design of effective and environmentally friendly pest control agents.
Used in Organic Synthesis:
Pyridin-2-yl(thiazol-2-yl)Methanone is employed as a versatile intermediate in organic synthesis, enabling the production of a diverse array of compounds with potential applications in various fields. Its unique structure and chemical properties contribute to the development of innovative and high-performing materials.
Check Digit Verification of cas no
The CAS Registry Mumber 90418-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,1 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90418-58:
(7*9)+(6*0)+(5*4)+(4*1)+(3*8)+(2*5)+(1*8)=129
129 % 10 = 9
So 90418-58-9 is a valid CAS Registry Number.
90418-58-9Relevant academic research and scientific papers
Synthesis of (Trimethylsilyl)thiazoles and Reactions with Carbonyl Compounds. Selectivity Aspects and Synthetic Utility
Dondoni, Alessandro,Fantin, Giancarlo,Fogagnolo, Marco,Medici, Alessandro,Pedrini, Paola
, p. 1748 - 1761 (2007/10/02)
Synthetic routes to all possible regioisomeric mono- and bis(trimethylsilyl)thiazoles as well as to the tris(trimethylsilyl) derivative via lithiation-silylation sequences of the thiazole ring followed by selective protodesilylation in some cases are described. (Trimethylsilyl)thiazoles serve as thiazolyl donor synthons upon reaction with carbonyl compounds (ketenes, acyl chlorides, aldehydes) for the preparation of mono- and bis-substituted thiazoles in very good yields.Carbodesilylation occurs more readily at the 2- than 5-position, whereas no reaction takes place at the 4-position.A mechanism via a thiazolium 2-ylide as an intermediate is suggested for the carbodesilylation at the 2-position.
