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Structure of 1213317-54-4
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This chiral amino alcohol features a sterically hindered aromatic moiety that enhances stability and influences stereoselective reactivity. The para-substituted phenyl ring imparts electron-rich character, while the primary amine and hydroxyl groups enable versatile functionalization. Designed for asymmetric synthesis applications, this bench-stable compound integrates readily into catalytic systems and serves as a key building block in pharmaceutical intermediates.
(S)-2-Amino-2-(3,5-dimethylphenyl)ethan-1-ol serves as a chiral building block for bioactive molecule synthesis, offering high functional group tolerance and bench stability. Its amino alcohol motif facilitates efficient derivatization in amide coupling, protection strategies, and cyclization reactions. The 3,5-dimethylphenyl group provides steric shielding and enhanced metabolic stability, making it valuable in the construction of heterocyclic scaffolds and pharmaceutical 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: