251-97-8 Usage
Uses
Used in Pharmaceutical Industry:
Imidazo[2,1-b]thiazole is utilized as a key intermediate in the synthesis of various pharmaceuticals for its diverse biological activities. Its antimicrobial, anti-inflammatory, and anticancer properties make it a valuable component in developing new drugs to combat a range of diseases.
Used in Agrochemical Industry:
In the agrochemical sector, Imidazo[2,1-b]thiazole serves as a crucial building block in the creation of compounds with pesticidal properties, contributing to the development of effective solutions for crop protection and management.
Used in Research Applications:
Imidazo[2,1-b]thiazole is employed as a fluorescent probe for the detection of metal ions in biological systems. This application is vital for research in areas such as bioinorganic chemistry, environmental science, and medical diagnostics, where the tracking and analysis of metal ions are essential.
Used in Medicinal Chemistry:
Imidazo[2,1-b]thiazole and its derivatives are of interest in medicinal chemistry due to their potential therapeutic applications. Imidazo[2,1-b]thiazole's unique structure and biological activities make it a promising candidate for the development of novel therapeutic agents targeting various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 251-97-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,5 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 251-97:
(5*2)+(4*5)+(3*1)+(2*9)+(1*7)=58
58 % 10 = 8
So 251-97-8 is a valid CAS Registry Number.
251-97-8Relevant academic research and scientific papers
The Preparation of Imidazothiazole, and Its 5-Substituted and 2,5-Disubstituted Analogues
Hopkinson, Christopher P.,Meakins, G. Denis,Purcell, Robert J.
, p. 1218 - 1227 (2007/10/02)
Imidazothiazole has been obtained in three steps (overall yield 21percent) from commercially available starting materials. 5-Substituted and 2,5-disubstituted imidazothiazoles are formed by sequences starting with the reactions of 2-aminothi
8-Hydroxy-hexahydronaphth[1',2':4,5]imidazo[2,1-b]thiazole and its derivatives
-
, (2008/06/13)
Hexahydronaphth[1',2':4,5]imidazo[2,1-b]thiazole and its derivatives of formula [I] STR1 (where X1 and X2 stand for hydrogen or halogen atoms; R represents a hydrogen atom, lower alkyl of 1 to 4 carbon atoms or lower alkyl substituted with a carboxyl given as --(CH2)n COOH (n is an integral number of 1 to 3); A, B, C, and D symbolize the rings respectively and the configuration of rings B and C is trans) and their acid adducts, and a method of preparing them according to the chemical equation given below: STR2 (where X3 is a halogen atom). These compounds have immunostimulative activity.
