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CAS 1334499-98-7

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Methyl 4′-amino-5-fluoro[1,1′-biphenyl]-3-carboxylate

Description:
Methyl 4′-amino-5-fluoro[1,1′-biphenyl]-3-carboxylate is an organic compound characterized by its biphenyl structure, which consists of two phenyl rings connected by a single bond. The presence of a methyl ester functional group at the carboxylic acid position contributes to its solubility in organic solvents. The compound features an amino group and a fluorine atom, which can influence its reactivity and biological activity. The amino group can participate in hydrogen bonding and may enhance the compound's interaction with biological targets, while the fluorine atom can affect lipophilicity and metabolic stability. This compound may be of interest in pharmaceutical research due to its potential applications in drug development, particularly in the design of molecules with specific biological activities. Its unique structural features suggest that it could exhibit interesting properties, such as altered pharmacokinetics or enhanced binding affinity to certain receptors. As with many organic compounds, its stability, reactivity, and potential applications would depend on the specific conditions under which it is studied.
Formula:C14H12FNO2
InChI:InChI=1S/C14H12FNO2/c1-18-14(17)11-6-10(7-12(15)8-11)9-2-4-13(16)5-3-9/h2-8H,16H2,1H3
InChI key:InChIKey=UHULQFJYWSPSQN-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1C=C(C=C(F)C1)C2=CC=C(N)C=C2
Synonyms:
  • Methyl 4′-amino-5-fluoro[1,1′-biphenyl]-3-carboxylate
  • [1,1′-Biphenyl]-3-carboxylic acid, 4′-amino-5-fluoro-, methyl ester
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