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Structure of 1212981-84-4
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This chiral building block features a (S)-configured amino alcohol scaffold flanked by a 3-fluoro-5-methoxyphenyl group, delivering enhanced stereochemical control in asymmetric synthesis. The electron-rich aromatic moiety, combined with the polar hydroxyl and amine functionalities, enables efficient coupling and derivatization under standard conditions. This bench-stable compound serves as a key intermediate in medicinal chemistry campaigns targeting CNS-active molecules and bioactive heterocycles.
(S)-2-Amino-2-(3-fluoro-5-methoxyphenyl)ethan-1-ol serves as a key chiral building block for bioactive molecule synthesis, leveraging its pendant amine and hydroxyl groups for functionalization. The 3-fluoro-5-methoxyphenyl moiety imparts metabolic stability and modulates electronic properties. This compound exhibits excellent bench stability, facilitates straightforward purification via crystallization or chromatography, and functions reliably in standard coupling and derivatization protocols used in medicinal chemistry workflows.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: