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Structure of 1060810-37-8
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This pyridylmethanamine features a chlorinated, methoxy-substituted pyridine core that enables selective coupling in late-stage functionalization. The primary amine group facilitates conjugation with electrophiles or polymer backbones, while the electron-withdrawing chlorine enhances reactivity in nucleophilic substitution cascades. This bench-stable derivative offers high solubility in common organic solvents and tolerates moisture during standard handling protocols.
(3-Chloro-6-methoxypyridin-2-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling the construction of pyridine-based scaffolds through standard coupling reactions. Its chloro and methoxy groups offer orthogonal reactivity for further functionalization, while the primary amine facilitates conjugation via amide bond formation or reductive amination. The compound exhibits good bench stability and is compatible with common purification methods, making it well-suited for iterative synthesis workflows in API development.
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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: