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Structure of 26847-01-8
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2-Chloro-4-methyl-1,3-thiazole is a bench-stable heterocyclic scaffold featuring a chlorine atom at the 2-position and a methyl group at the 4-position, enabling selective functionalization. This electron-deficient thiazole integrates readily into medicinal chemistry libraries, serving as a key building block for kinase inhibitors and bioactive compounds.
2-Chloro-4-methyl-1,3-thiazole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The chloro group at C2 enables nucleophilic substitution reactions, while the methyl substituent at C4 enhances regioselectivity in downstream functionalizations. Its stability under standard reaction conditions and compatibility with common coupling protocols make it a practical choice for constructing thiazole-based scaffolds in API development and process chemistry workflows.
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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-H312-H332-H227
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Precautionary Statements : P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P501
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Lot numbers can be found on the outside label of a product: