Real-time FTIR spectroscopy and in situ dynamic rheology were used to characterize the UV curing kinetics of a thiol-ene system containing trimethylolpropane tris(2-mercaptoacetate) and trimethylolpropane diallyl ether. The combination of these two techniques offered a powerful approach for monitoring changes in the chemical and rheological properties of the system during UV curing. Comparable gel times were independently obtained from both FTIR spectroscopy and rheology, thereby validating the comparison of data obtained from each method. The thiol conversion determined from FTIR spectroscopy was correlated with the elastic modulus obtained from theology. The conversion increased very rapidly during the initial stages of UV curing. However, the elastic modulus did not have an appreciable value until after 65% of the thiol functional groups have reacted, following which the elastic modulus increased at a rapid rate. From the Flory-Stockmayer theory of gelation, the critical thiol conversion at the gel point was determined to be 0.71. This indicated that the elastic modulus had an appreciable value only when the sample is close to its gel point, consistent with the step growth kinetics of the polymerization reaction. From the conversion data. the photoinitiated thiol-ene reaction tvas determined to be a second-order reaction. This second-order behavior was inconsistent with the termination mechanisms currently found in Literature. A possible reason for such a discrepancy is discussed.