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Structure of 17289-30-4
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This imidazole derivative features a chloromethyl group enabling efficient functionalization, paired with a methylated nitrogen enhancing solubility and stability. The hydrochloride salt form ensures excellent handling and shelf life under standard conditions.
4-(Chloromethyl)-1-methyl-1H-imidazole hydrochloride serves as a versatile bifunctional building block in medicinal chemistry and synthetic organic chemistry. The chloromethyl group enables efficient alkylation reactions, while the protonated imidazole moiety enhances solubility and facilitates salt formation. It functions reliably in nucleophilic substitution cascades, heterocycle functionalization, and conjugate additions, offering excellent bench stability and straightforward purification. This reagent is particularly valuable for constructing imidazole-based pharmacophores and targeted covalent inhibitors.
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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#: 3261
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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: