The synthesis, chemical characterization and optical properties of 2-(1-naphthyl)-4-vinyl-5phenyloxazole (vNPO) and 2-(1-naphthyl)-4-allyl-5-phenyloxazole (allylNPO) monomers are reported.Starting with the organic fluor 2-(1-naphthyl)-5-phenyloxazole (aNPO), the vNPO and allylNPO monomers were synthesized using Stille coupling followed by purification. The final products were obtained with yields of B95% and B55% for vNPO and allylNPO. The absorption/emission spectra of aNPO, vNPO and allylNPO revealed that vNPO has the largest red-shifted in emission with an average wavelength of B420 nm, which is an advantage for increasing photomultiplier tube sensitivity without the need to add a wavelength shifter. Stable scintillating resin beads were prepared through copolymerization of the newly synthesized fluor monomers with styrene or 4-methylstyrene and divinylbenzene in the presence of toluene porogen. The resin beads were chemically stable and retained the ability to scintillate efficiently after energy deposition of beta particles from 99 Tc. This result indicates efficient energy transfer occurs from the base polymer to the covalently attached fluors with subsequent fluorescence in the presence of ionizing radiation. † Electronic supplementary information (ESI) available: Listing of chemical analysis, scintillation measurement setup, 13 C spectra, GCMS chromatograms, optical image for the plastic beads and absorption/emission spectra. See Scheme 1 Synthesis of monomer 2-(1-naphthyl)-4-vinyl-5-phenyloxazole (vNPO) and 2-(1-naphthyl)-4-allyl-5-phenyloxazole (allylNPO).