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Structure of 15960-05-1
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(S)-2-Amino-4,4,4-trifluorobutanoic acid features a chiral α-amino acid scaffold with a trifluoromethyl group at the γ-position, imparting enhanced metabolic stability and altered electronic properties. This configuration delivers a potent bioisostere for glutamic acid, enabling precise incorporation into peptidomimetics and enzyme substrates where modulated polarity and conformational rigidity are critical.
(S)-2-Amino-4,4,4-trifluorobutanoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and peptide-based drug discovery. The trifluoromethyl group imparts enhanced metabolic stability and membrane permeability, while the amino and carboxylic acid functionalities enable straightforward derivatization via amide bond formation or incorporation into peptidomimetics. Its bench-stable solid form facilitates handling and purification, making it well-suited for scalable 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: