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Structure of 1415380-62-9
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(S)-1-(2,3-Difluorophenyl)ethanamine features a chiral α-amino center paired with a 2,3-difluorophenyl group, delivering enhanced metabolic stability and improved binding selectivity in bioactive molecule design. This bench-stable, moisture-tolerant amine integrates readily into asymmetric synthesis workflows for pharmaceutical intermediates.
(S)-1-(2,3-Difluorophenyl)ethanamine serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of enantiopure pharmaceutical intermediates. Its structural motif—featuring a stereogenic center adjacent to a difluorinated aromatic ring—confers enhanced metabolic stability and modulated lipophilicity. The molecule exhibits good bench stability, facilitates straightforward purification via distillation or crystallization, and participates reliably in standard amine functionalizations, including acylation, alkylation, and coupling reactions. This compound functions as a key scaffold for constructing bioactive heterocycles and targeted small-molecule candidates.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P210-P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: