CAS 914200-00-3

2-(3,5-Difluorophenoxy)ethanamine

Description:

2-(3,5-Difluorophenoxy)ethanamine is an organic compound characterized by its structure, which includes an ethanamine backbone substituted with a 3,5-difluorophenoxy group. This compound features a phenyl ring with two fluorine atoms positioned at the 3 and 5 positions, enhancing its lipophilicity and potentially influencing its biological activity. The presence of the amino group (-NH2) in the ethanamine portion suggests that it may participate in hydrogen bonding, making it soluble in polar solvents. The fluorine substituents can also affect the compound's electronic properties, potentially impacting its reactivity and interaction with biological targets. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its unique structural features that could confer specific biological activities. As with many fluorinated compounds, it may exhibit enhanced metabolic stability and altered pharmacokinetics. However, detailed studies would be necessary to fully understand its properties and potential applications.

Formula: C₈H₉F₂NO

InChI: InChI=1S/C8H9F2NO/c9-6-3-7(10)5-8(4-6)12-2-1-11/h3-5H,1-2,11H2

InChI key: InChIKey=OVEITJSDGWRVLP-UHFFFAOYSA-N

SMILES: O(CCN)C1=CC(F)=CC(F)=C1

Synonyms:

• 2-(3,5-Difluorophenoxy)ethanamine
• 2-(3,5-Difluorophenoxy)ethan-1-amine
• Ethanamine, 2-(3,5-difluorophenoxy)-