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Structure of 1213594-37-6
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(1S)-1-(6-Bromo(3-pyridyl))ethylamine features a chiral center with a brominated pyridyl group, enabling selective functionalization in asymmetric synthesis. The pendant amine facilitates coupling reactions, while the electron-deficient pyridine ring enhances reactivity in transition-metal-catalyzed transformations. This configuration delivers high enantioselectivity in pharmaceutical intermediates.
(1S)-1-(6-Bromopyridin-3-yl)ethanamine serves as a versatile building block for medicinal chemistry and catalytic synthesis, enabling direct incorporation of brominated pyridine motifs into target molecules. Its chiral α-aminoethyl scaffold facilitates efficient coupling reactions and supports downstream functionalization via the pendant bromide. The compound exhibits excellent bench stability, simplifies purification, and demonstrates broad compatibility with standard cross-coupling protocols and heterocycle construction methods.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: