CAS 688-19-7
:5-Methyl hydrogen N-(2,2,2-trifluoroacetyl)-L-glutamate
Description:
5-Methyl hydrogen N-(2,2,2-trifluoroacetyl)-L-glutamate, with the CAS number 688-19-7, is a derivative of the amino acid L-glutamate, modified to include a trifluoroacetyl group and a methyl group. This compound typically exhibits characteristics associated with amino acids, such as the ability to form hydrogen bonds due to the presence of both carboxylic acid and amine functional groups. The trifluoroacetyl moiety contributes to its unique chemical properties, including increased lipophilicity and potential for enhanced biological activity. The presence of the methyl group can influence the steric and electronic properties of the molecule, potentially affecting its interaction with biological targets. This compound may be utilized in various biochemical applications, including as a building block in peptide synthesis or as a tool in studying glutamate receptors. Its stability, solubility, and reactivity can vary based on environmental conditions such as pH and temperature, making it important to consider these factors in experimental settings.
Formula:C8H10F3NO5
InChI:InChI=1S/C8H10F3NO5/c1-17-5(13)3-2-4(6(14)15)12-7(16)8(9,10)11/h4H,2-3H2,1H3,(H,12,16)(H,14,15)/t4-/m0/s1
InChI key:InChIKey=CHUMJXZJCBKVKH-BYPYZUCNSA-N
SMILES:[C@H](NC(C(F)(F)F)=O)(CCC(OC)=O)C(O)=O
Synonyms:- L-Glutamic acid, N-(trifluoroacetyl)-, 5-methyl ester
- Glutamic acid, N-(trifluoroacetyl)-, 5-methyl ester
- Glutamic acid, N-(trifluoroacetyl)-, 5-methyl ester, L-
- L-Glutamic acid, N-(2,2,2-trifluoroacetyl)-, 5-methyl ester
- 5-Methyl hydrogen N-(2,2,2-trifluoroacetyl)-L-glutamate
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