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Structure of 57892-76-9
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2-(Chloromethyl)imidazo[1,2-a]pyridine features a reactive chloromethyl group appended to an imidazo[1,2-a]pyridine core, enabling efficient alkylation under mild conditions. This heterocyclic scaffold combines moderate electron density with enhanced stability, facilitating incorporation into bioconjugation workflows and medicinal chemistry libraries.
2-(Chloromethyl)imidazo[1,2-a]pyridine serves as a versatile bifunctional building block in medicinal chemistry, enabling efficient incorporation of imidazo[1,2-a]pyridine scaffolds into target molecules. The chloromethyl group facilitates nucleophilic substitution reactions with amines, thiols, and other soft nucleophiles, offering reliable access to diverse derivatives. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for iterative synthesis campaigns and library generation.
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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 : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: