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Structure of 71670-70-7
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2-(Chloromethyl)-5-methyl-Pyridine hydrochloride features a chloromethyl group at the 2-position of a pyridine ring bearing a methyl substituent at the 5-position. This electron-deficient heterocycle enables selective alkylation reactions under mild conditions, offering enhanced reactivity in synthetic transformations. The hydrochloride salt ensures improved solubility and stability for handling in aqueous or polar organic media.
2-(Chloromethyl)-5-methyl-pyridine hydrochloride serves as a versatile building block for the synthesis of pharmaceutical intermediates and functionalized heterocycles. The chloromethyl group enables efficient nucleophilic substitution, while the pyridine nitrogen provides a handle for metal coordination or derivatization. Its bench-stable hydrochloride salt form enhances handling and purification, offering good functional group tolerance in standard coupling and alkylation workflows.
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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-P363-P405-P501
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Lot numbers can be found on the outside label of a product: