structure of Tert-butyl (4-fluorophenyl)glycinate

Tert-butyl (4-fluorophenyl)glycinate

CAS No.: 1184105-23-4
M. Wt: 225.26
M. Fa: C12H16FNO2
InChI Key: CJXPMCMRRYUEME-UHFFFAOYSA-N

Names and Identifiers of Tert-butyl (4-fluorophenyl)glycinate

CAS Number

1184105-23-4

IUPAC Name

tert-butyl 2-(4-fluoroanilino)acetate

InChI

InChI=1S/C12H16FNO2/c1-12(2,3)16-11(15)8-14-10-6-4-9(13)5-7-10/h4-7,14H,8H2,1-3H3

InChIKey

CJXPMCMRRYUEME-UHFFFAOYSA-N

Canonical SMILES

CC(C)(C)OC(=O)CNC1=CC=C(C=C1)F

Physical and chemical properties of Tert-butyl (4-fluorophenyl)glycinate

Boiling Point

295.0±20.0 °C(Predicted)

Density

1.131±0.06 g/cm3(Predicted)

Molecular Formula

C12H16FNO2

Molecular Weight

225.26

Applications of Tert-butyl (4-fluorophenyl)glycinate

Tert-butyl (4-fluorophenyl)glycinate has several notable applications:

  • Pharmaceutical Development: It serves as an intermediate in the synthesis of bioactive compounds and pharmaceuticals.
  • Organic Synthesis: The compound is utilized in various organic reactions, contributing to the development of complex molecules in research settings.
  • Research Tool: Its unique properties make it valuable for studying enzyme mechanisms and receptor interactions within biological systems.

Interaction Studies of Tert-butyl (4-fluorophenyl)glycinate

Interaction studies involving tert-butyl (4-fluorophenyl)glycinate focus on its binding affinity and activity against specific biological targets. Preliminary data suggest that it may influence metabolic pathways related to amino acid metabolism and neurotransmitter function. Further research is needed to elucidate its precise interactions and therapeutic potential.