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Structure of 1213343-02-2
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This chiral building block features a (R)-configured amino alcohol scaffold flanked by a 3-fluoro-5-methoxyphenyl group, delivering enhanced solubility and stability under standard bench conditions. The electron-rich aromatic ring and polar functional groups enable efficient coupling in asymmetric synthesis, while the stereochemical integrity supports high-fidelity incorporation into complex molecular architectures.
(R)-2-Amino-2-(3-fluoro-5-methoxyphenyl)ethan-1-ol serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through established amine and alcohol functional group transformations. Its bench-stable nature, combined with orthogonal reactivity and tolerance to standard coupling conditions, facilitates efficient incorporation into diverse heterocyclic scaffolds and API intermediates.
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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: