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Structure of 1228559-00-9
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This chiral amine features a strategically positioned bromine and fluorine substituent on the aromatic ring, enabling selective functionalization in medicinal chemistry. The α-methyl group imparts stereochemical stability, while the amine handle facilitates conjugation in target-directed synthesis.
(αS)-4-Bromo-2-fluoro-α-methylbenzenemethanamine serves as a valuable chiral building block for the synthesis of bioactive molecules, enabling stereoselective incorporation of fluorinated aryl motifs. Its functional group tolerance facilitates downstream coupling reactions, while the α-methyl substitution enhances metabolic stability. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, making it well-suited for medicinal chemistry campaigns requiring fluorinated phenylalanine analogs.
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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 : 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: