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Structure of 1001094-89-8
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(S)-4-(1-Aminoethyl)phenol hydrobromide features a chiral benzylic amine moiety with enhanced solubility and stability in aqueous environments. This bench-stable derivative integrates readily into asymmetric synthesis workflows, offering precise stereocontrol at the α-carbon position. The para-hydroxyl group enables further functionalization via coupling or oxidation reactions.
(S)-4-(1-Aminoethyl)phenol hydrobromide serves as a chiral building block for pharmaceutical intermediates, enabling direct access to aryl-amine-containing scaffolds via standard coupling reactions. The hydrobromide salt enhances solubility and stability in aqueous and polar organic media, facilitating purification and handling. Its functional group tolerance supports downstream transformations including Suzuki-Miyaura coupling and amide formation, making it a practical choice for iterative synthesis 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: