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Structure of 53572-98-8
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Imidazo[2,1-b]thiazole-6-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 6-position, enabling direct conjugation or derivatization. This scaffold combines electronic rigidity with enhanced solubility and stability under standard bench conditions, making it valuable for medicinal chemistry and materials synthesis applications.
Imidazo[2,1-b]thiazole-6-carboxylic acid serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of bioactive scaffolds through standard coupling reactions. Its carboxylic acid functionality facilitates direct amidation, esterification, and derivatization under mild conditions. The fused imidazo[2,1-b]thiazole core exhibits enhanced metabolic stability and favorable pharmacokinetic properties, making it a practical component in the synthesis of kinase inhibitors and other targeted therapeutics. Bench-stable and readily purified by recrystallization or chromatography, it supports scalable workflows in drug discovery and process development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: