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Structure of 135206-76-7
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This chloromethyl-substituted triazole hydrochloride delivers a reactive handle for nucleophilic functionalization, enabling efficient conjugation in bioconjugate chemistry and medicinal discovery. The quaternary nitrogen enhances solubility and stability under standard conditions, while the chloromethyl group facilitates site-specific derivatization.
3-(Chloromethyl)-1-methyl-1H-1,2,4-triazole hydrochloride serves as a versatile electrophilic building block for the synthesis of triazolyl alkyl derivatives. The chloromethyl group enables efficient nucleophilic substitution reactions, facilitating the construction of bioactive heterocyclic scaffolds. Its bench-stable solid form and high functional group tolerance make it well-suited for iterative coupling strategies in medicinal chemistry and process development workflows.
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Lot numbers can be found on the outside label of a product: