25944-60-9 Usage
Uses
Used in Pharmaceutical Industry:
3,6-Dimethylimidazo[2,1-b]thiazole is used as an intermediate in the synthesis of various pharmaceuticals due to its unique structure and biological activities. It plays a crucial role in the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
3,6-DiMethyliMidazo[2,1-b]thiazole is also utilized as an intermediate in the synthesis of agrochemicals, particularly those with antimicrobial and antiviral properties. Its application in this industry helps in the development of effective pesticides and other agricultural products.
Used in Dye Industry:
3,6-Dimethylimidazo[2,1-b]thiazole is used as a precursor for the synthesis of fluorescent dyes. Its unique structure allows for the creation of dyes with specific properties, making it valuable in various applications that require fluorescence.
Used in Photochemistry:
3,6-Dimethylimidazo[2,1-b]thiazole has been studied for its potential use as a sensitizing agent in photochemistry. Its ability to enhance the efficiency of photochemical reactions makes it a promising candidate for applications in this field.
Used in Antitumor Applications:
Due to its antitumor properties, 3,6-Dimethylimidazo[2,1-b]thiazole is being investigated for its potential use in the development of anticancer drugs. Its ability to target and inhibit tumor growth could lead to the creation of novel therapeutic agents for cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 25944-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,4 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25944-60:
(7*2)+(6*5)+(5*9)+(4*4)+(3*4)+(2*6)+(1*0)=129
129 % 10 = 9
So 25944-60-9 is a valid CAS Registry Number.
25944-60-9Relevant academic research and scientific papers
Ligand-free copper-catalyzed regioselective C-2 arylation of imidazo[2,1-b]thiazoles
Huang, Guoli,Sun, Hongsheng,Qiu, Xiaojie,Jin, Can,Lin, Chen,Shen, Yingzhong,Jiang, Juli,Wang, Leyong
supporting information; experimental part, p. 5224 - 5227 (2011/12/04)
An effective, regioselective C-2 arylation of imidazo[2,1-b]thiazoles catalyzed by Cu(I) has been developed. This arylation proceeded smoothly without promotion of the ligands, and various functional (22 samples) groups were well tolerated. Preliminary mechanistic studies of this arylation are also reported.
Substituted imidazo[2,1-b]thiazoles from 2-aminothiazoles and α-bromo ketones: Efficient preparation and proof of structure
Meakins, G. Denis,Musk, Sally R. R.,Robertson, Colin A.,Woodhouse, Lee S.
, p. 643 - 648 (2007/10/02)
The salts formed from α-aminothiazoles and α-bromo ketones (RCOCH2Br) have been basified, and the products converted into amides. Examination of the amides established that they are 2-acylimino-2,3- dihydrothiazoles rather than 2-acylaminothiaz
