CAS 369-08-4
:N-(2,2,2-Trifluoroacetyl)-L-aspartic acid
Description:
N-(2,2,2-Trifluoroacetyl)-L-aspartic acid, with the CAS number 369-08-4, is an amino acid derivative characterized by the presence of a trifluoroacetyl group attached to the nitrogen of the aspartic acid backbone. This compound is notable for its fluorinated acyl group, which imparts unique chemical properties, including increased lipophilicity and altered reactivity compared to non-fluorinated analogs. It is typically a white to off-white crystalline solid, soluble in polar solvents such as water and methanol, due to the presence of the carboxylic acid and amino groups. The trifluoroacetyl moiety enhances its potential as a biochemical probe or in medicinal chemistry applications, particularly in the development of pharmaceuticals targeting specific biological pathways. Additionally, the compound may exhibit interesting interactions with biological macromolecules, making it a subject of interest in research related to drug design and protein-ligand interactions. Proper handling and storage are essential, as with many fluorinated compounds, to ensure safety and stability.
Formula:C6H6F3NO5
InChI:InChI=1S/C6H6F3NO5/c7-6(8,9)5(15)10-2(4(13)14)1-3(11)12/h2H,1H2,(H,10,15)(H,11,12)(H,13,14)/t2-/m0/s1
InChI key:InChIKey=NTFULCXLYCSQIW-REOHCLBHSA-N
SMILES:[C@H](NC(C(F)(F)F)=O)(CC(O)=O)C(O)=O
Synonyms:- Aspartic acid, N-(trifluoroacetyl)-, L-
- L-Aspartic acid, N-(2,2,2-trifluoroacetyl)-
- L-Aspartic acid, N-(trifluoroacetyl)-
- N-(2,2,2-Trifluoroacetyl)-L-aspartic acid
- N-Trifluoroacetyl-L-aspartic acid
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