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Structure of 90773-41-4
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This chloromethyl-imidazole derivative features a reactive chloromethyl group positioned adjacent to a methylated imidazole core, enabling efficient coupling in bioconjugation and polymer functionalization. The hydrochloride salt enhances solubility and stability under standard handling conditions.
5-(Chloromethyl)-1-methyl-1H-imidazole hydrochloride serves as a versatile bifunctional building block in medicinal chemistry, enabling efficient introduction of both alkylating and heterocyclic moieties. The chloromethyl group facilitates nucleophilic substitution reactions under mild conditions, while the protonated imidazole ring enhances solubility and stability in aqueous media. This compound functions reliably in on-resin modifications, late-stage functionalization, and the construction of imidazolyl-containing scaffolds found in bioactive molecules.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: