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Structure of 38585-61-4
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4-(Chloromethyl)-1H-imidazole hydrochloride features a reactive chloromethyl group attached to the imidazole ring, enabling efficient alkylation under mild conditions. This bench-stable derivative delivers high functional group compatibility and facilitates rapid conjugation in synthetic workflows.
4-(Chloromethyl)-1H-imidazole hydrochloride serves as a versatile building block for imidazole-based scaffolds, enabling efficient functionalization via nucleophilic substitution. Its chloromethyl group exhibits high reactivity toward amines, thiols, and other nucleophiles under mild conditions, facilitating rapid access to conjugated derivatives. The hydrochloride salt enhances solubility and stability in aqueous and polar organic media, supporting straightforward handling and purification. This compound functions as a key intermediate in the synthesis of bioactive heterocycles and targeted ligands.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: