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Structure of 1212942-90-9
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(R)-1-(6-Bromopyridin-3-yl)ethanamine features a chiral ethylamine handle attached to a brominated pyridine ring, enabling selective coupling in asymmetric synthesis. The para-bromo substituent provides a reactive handle for cross-coupling transformations, while the (R)-stereochemistry ensures high enantioselectivity in downstream applications. This bench-stable, moisture-tolerant amine integrates efficiently into complex molecular architectures.
(R)-1-(6-Bromopyridin-3-yl)ethanamine serves as a versatile chiral building block for the synthesis of pyridine-containing pharmaceutical intermediates. Its bromo group enables palladium-catalyzed coupling reactions, while the chiral amine functionality provides stereochemical control in target-directed synthesis. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in medicinal chemistry campaigns requiring stereoselective heterocyclic scaffold assembly.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: