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CAS 1256359-14-4

:

Phenylmethyl N-[2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate

Description:
Phenylmethyl N-[2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate is a synthetic organic compound characterized by its complex structure, which includes a carbamate functional group and a boron-containing moiety. The presence of the fluorine atom and the dioxaborolane ring contributes to its unique chemical properties, potentially enhancing its reactivity and solubility in various solvents. This compound may exhibit specific biological activities, making it of interest in pharmaceutical research and development. Its molecular structure suggests potential applications in medicinal chemistry, particularly in drug design, where the incorporation of boron can influence the compound's interaction with biological targets. Additionally, the presence of the tetramethyl group may affect the steric and electronic properties, influencing its overall stability and reactivity. As with many synthetic compounds, safety and handling precautions are essential due to potential toxicity or environmental impact. Further studies would be necessary to fully elucidate its characteristics, including its physical properties, reactivity, and potential applications in various fields.
Formula:C20H23BFNO4
InChI:InChI=1S/C20H23BFNO4/c1-19(2)20(3,4)27-21(26-19)15-10-11-16(22)17(12-15)23-18(24)25-13-14-8-6-5-7-9-14/h5-12H,13H2,1-4H3,(H,23,24)
InChI key:InChIKey=NSRXSBHAUAOESX-UHFFFAOYSA-N
SMILES:N(C(OCC1=CC=CC=C1)=O)C=2C=C(C=CC2F)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • Carbamic acid, N-[2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, phenylmethyl ester
  • Phenylmethyl N-[2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
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