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Structure of 861036-67-1
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Quinolin-2-ylmethanamine hydrochloride features a quinoline scaffold with a primary amine tethered to a methylene linker, delivering enhanced solubility and stability. This bench-stable derivative enables direct incorporation into medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds, where the nitrogen-rich heterocycle facilitates key hydrogen bonding interactions.
Quinolin-2-ylmethanamine hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to quinoline-based scaffolds through standard amine coupling and functionalization reactions. The hydrochloride salt enhances bench stability and solubility, facilitating purification and handling in multi-step syntheses. Its reactivity supports diverse transformations including reductive amination, acylation, and heterocycle formation, making it well-suited for the construction of biologically active compounds and API intermediates.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: