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CAS 467442-20-2

:

(2S)-2-(tert-butoxycarbonylamino)-4,4-difluoro-butanoic acid

Description:
(2S)-2-(tert-butoxycarbonylamino)-4,4-difluoro-butanoic acid is an amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group on the amino group, which enhances its stability and solubility in organic solvents. The molecule features a difluorinated butanoic acid backbone, contributing to its unique chemical properties, such as increased lipophilicity and potential bioactivity. The presence of fluorine atoms can influence the compound's reactivity and interaction with biological systems, making it of interest in medicinal chemistry and drug design. The stereochemistry at the 2-position (S configuration) is crucial for its biological activity, as it can affect how the molecule interacts with enzymes and receptors. This compound is typically used in peptide synthesis and as an intermediate in the development of pharmaceuticals. Its solubility profile, stability under various conditions, and reactivity with other functional groups are important characteristics that dictate its applications in chemical research and development.
Formula:C9H15F2NO4
InChI:InChI=1/C9H15F2NO4/c1-9(2,3)16-8(15)12-5(7(13)14)4-6(10)11/h5-6H,4H2,1-3H3,(H,12,15)(H,13,14)/t5-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](CC(F)F)C(=O)O)O
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