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Structure of 262295-96-5
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(6-Methoxypyridin-3-yl)methanamine features a pyridine core with a methoxy group at the 6-position and a primary amine at the 3-position, enabling direct conjugation or functionalization. This electron-rich heterocycle enhances solubility and reactivity in transition-metal-catalyzed cross-coupling reactions. The pendant amine facilitates derivatization for bioconjugation, material synthesis, or pharmaceutical intermediates. Bench-stable under standard conditions, it integrates seamlessly into multi-step synthetic sequences.
(6-Methoxypyridin-3-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through standard amine functionalization. Its ortho-methoxy group enhances electron density at the pyridine ring, facilitating nucleophilic substitution and transition-metal-catalyzed coupling reactions. The primary amine functionality offers straightforward derivatization via acylation, alkylation, or reductive amination, while the compound exhibits good bench stability and compatibility with common purification methods.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H318-H335
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: