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Structure of 120740-08-1
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2-Chloro-5-aminomethylthiazole features a reactive chloro substituent and a primary amine handle, enabling straightforward functionalization in medicinal chemistry. This bench-stable heterocycle integrates readily into bioactive scaffolds, particularly in kinase inhibitor development and targeted drug discovery workflows.
2-Chloro-5-aminomethylthiazole serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the thiazole ring via nucleophilic substitution. The chloro group facilitates coupling reactions with amines, thiols, and heterocycles under mild conditions, while the aminomethyl side chain offers a handle for further derivatization. Bench-stable and compatible with standard purification methods, it functions efficiently in the synthesis of thiazole-based pharmacophores and API intermediates.
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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: