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Structure of 140373-17-7
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2-Amino-2-(4-fluorophenyl)ethan-1-ol features a chiral center flanked by an amino group and a hydroxyl function, enabling its use in asymmetric synthesis. The para-fluorophenyl moiety imparts enhanced electronic effects and metabolic stability. This bench-stable compound integrates readily into pharmaceutical intermediates and serves as a key scaffold for bioactive molecule construction.
2-Amino-2-(4-fluorophenyl)ethan-1-ol serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of fluorinated amino alcohols and β-amino alcohol pharmacophores. Its bench-stable nature, combined with orthogonal functionality for further derivatization, facilitates efficient access to heterocyclic scaffolds and API intermediates via standard coupling, cyclization, or protection strategies.
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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: