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CAS 108321-84-2

:

L-phenylalanine 4-methyl-7-coumarinyl-amide trifluoroac.

Description:
L-phenylalanine 4-methyl-7-coumarinyl-amide trifluoroacetic acid, identified by the CAS number 108321-84-2, is a synthetic compound that combines the amino acid L-phenylalanine with a coumarin derivative. This compound typically exhibits characteristics associated with both its amino acid and coumarin components, such as potential fluorescence due to the coumarin moiety, which is known for its strong light absorption and emission properties. The trifluoroacetic acid component suggests that the compound may have enhanced solubility in organic solvents and could exhibit acidic properties. In biological contexts, derivatives of L-phenylalanine are often studied for their roles in protein synthesis and as precursors to neurotransmitters. The presence of the coumarin structure may also indicate potential applications in photochemistry or as a fluorescent probe in biochemical assays. Overall, this compound's unique structure may confer specific reactivity and interaction profiles, making it of interest in both chemical and biological research.
Formula:C21H19F3N2O5
InChI:InChI=1/C19H18N2O3.C2HF3O2/c1-12-9-18(22)24-17-11-14(7-8-15(12)17)21-19(23)16(20)10-13-5-3-2-4-6-13;3-2(4,5)1(6)7/h2-9,11,16H,10,20H2,1H3,(H,21,23);(H,6,7)/t16-;/m0./s1
SMILES:Cc1cc(=O)oc2cc(ccc12)N=C([C@H](Cc1ccccc1)N)O.C(=O)(C(F)(F)F)O
Synonyms:
  • L-Phenylalanine 4-methyl-7-coumarinylamide trifluoroacetate salt
  • L-Phenylalanine 7-amido-4-methylcoumarin trifluoroacetate salt
  • H-Phe-AMC . TFA
  • N-(4-methyl-2-oxo-2H-chromen-7-yl)-L-phenylalaninamide trifluoroacetate
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