6-Chloro-2,3-dimethylimidazo[2,1-b]thiazole
[CAS# 135718-49-9]

Identification

• Classification: Chemical reagent >> Organic reagent >> Amide
• Name: 6-Chloro-2,3-dimethylimidazo[2,1-b]thiazole
• Molecular Formula: C₇H₇ClN₂S
• Molecular Weight: 186.66
• CAS Registry Number: 135718-49-9
• SMILES: CC1=C(SC2=NC(=CN12)Cl)C

Properties

• Density: 1.5±0.1 g/cm³, Calc.^*
• Index of Refraction: 1.703, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Discovory and Applicatios

6-Chloro-2,3-dimethylimidazo[2,1-b]thiazole is a chemical compound recognized for its distinctive structure and applications in chemical research and industry. This molecule belongs to the imidazo[2,1-b]thiazole class, characterized by a fused ring system that combines imidazole and thiazole rings, along with additional substituents that influence its chemical behavior.

The discovery of 6-Chloro-2,3-dimethylimidazo[2,1-b]thiazole stems from efforts to explore the properties and reactivity of fused heterocyclic systems. The compound features a chlorine atom and two methyl groups attached to the imidazo[2,1-b]thiazole framework. This specific arrangement of substituents affects the molecule's electronic properties and its interactions in chemical reactions.

In medicinal chemistry, 6-Chloro-2,3-dimethylimidazo[2,1-b]thiazole is of particular interest due to its potential as a lead compound for drug development. The imidazo[2,1-b]thiazole ring system is known for its biological activities, including anticancer and antimicrobial effects. Researchers are studying how the introduction of chlorine and methyl groups influences these activities to develop new therapeutic agents. For instance, modifications to this structure could lead to compounds that selectively target cancer cells or bacterial pathogens, providing new treatment options.

Beyond its medicinal applications, 6-Chloro-2,3-dimethylimidazo[2,1-b]thiazole is also valuable in chemical research and materials science. Its ability to participate in various chemical reactions makes it a useful intermediate in the synthesis of more complex molecules. This compound is employed in the development of novel organic materials and specialty chemicals, where its unique ring system contributes to the properties of the final products.

The compound is also utilized to study the reactivity and stability of heterocyclic systems. Its structure offers a basis for examining how different substituents affect the chemical and physical properties of imidazo[2,1-b]thiazole derivatives. Such research can lead to the discovery of new compounds with enhanced or novel functionalities.

In summary, 6-Chloro-2,3-dimethylimidazo[2,1-b]thiazole is a versatile compound with significant implications for drug development and industrial chemistry. Its unique structure and reactivity make it a valuable tool for researchers aiming to create new therapeutic agents and advanced materials. Ongoing studies are likely to reveal further applications and innovations involving this compound.