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Structure of 240409-02-3
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This amino acid derivative features a sterically hindered aryl group that enhances metabolic stability. The 2,4-difluorophenyl moiety imparts electron-withdrawing character, influencing reactivity and solubility. Designed for synthetic applications in medicinal chemistry, it serves as a key scaffold for bioactive compound development.
2-Amino-2-(2,4-difluorophenyl)acetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and peptide-like scaffolds. Its ortho-difluoro substitution enhances metabolic stability and modulates electronic properties, while the α-amino carboxylic acid functionality supports direct incorporation into peptidomimetics and CNS-targeted compounds. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for high-throughput synthetic 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-H320-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: