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CAS 1346597-49-6

:

2,2-Difluoro-3-[methyl(phenylmethyl)amino]propanoic acid

Description:
2,2-Difluoro-3-[methyl(phenylmethyl)amino]propanoic acid is a synthetic organic compound characterized by its unique structure, which includes a propanoic acid backbone substituted with two fluorine atoms and a methyl(phenylmethyl)amino group. The presence of the difluoro substituents enhances its lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. The compound is likely to exhibit acidic properties due to the carboxylic acid functional group, which can donate protons in solution. Its molecular structure suggests potential interactions with biological targets, possibly affecting enzyme activity or receptor binding. Additionally, the presence of both fluorine and aromatic groups may contribute to its stability and reactivity. As with many fluorinated compounds, it may also exhibit unique solubility characteristics in various solvents. Overall, 2,2-Difluoro-3-[methyl(phenylmethyl)amino]propanoic acid represents a class of compounds that could have significant implications in medicinal chemistry and drug development.
Formula:C11H13F2NO2
InChI:InChI=1S/C11H13F2NO2/c1-14(8-11(12,13)10(15)16)7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3,(H,15,16)
InChI key:InChIKey=YGGZLMKMZYHUKA-UHFFFAOYSA-N
SMILES:C(N(CC(C(O)=O)(F)F)C)C1=CC=CC=C1
Synonyms:
  • 2,2-Difluoro-3-[methyl(phenylmethyl)amino]propanoic acid
  • Propanoic acid, 2,2-difluoro-3-[methyl(phenylmethyl)amino]-
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