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Structure of 344413-79-2
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(2R)-3-Amino-2-fluoropropan-1-ol is a chiral fluorinated amino alcohol featuring a stereodefined (2R) configuration. This bench-stable derivative integrates a primary hydroxyl group and a primary amine, enabling efficient coupling and functionalization in synthetic sequences. The fluorine atom imparts enhanced metabolic stability and modulates electronic properties, making it valuable for bioactive molecule synthesis.
(2R)-3-Amino-2-fluoropropan-1-ol serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of fluorinated amino alcohols with defined stereochemistry. Its stability under standard reaction conditions and compatibility with common functional groups facilitate straightforward incorporation into complex molecular architectures. The molecule functions effectively in nucleophilic substitution and coupling reactions, offering reliable access to bioactive scaffolds relevant to CNS-targeted therapeutics and kinase inhibitors.
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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: