A high-resolution rotational coherence spectroscopy (RCS) investigation of para-cyclohexylaniline (pCHA) was performed using the methods of time-resolved stimulated Raman-induced fluorescence depletion (TRSRFD) and time-resolved stimulated emission pumping (TRSEP). TRSRFD and TRSEP are sensitive to ground state or excited state rotational constants, respectively and allow the deconvolution of the time-resolved fluorescence depletion (TRFD) spectrum to which both ground state and excited state rotational constants contribute. Moreover, from a detailed analysis of the presented experimental data it is deduced, that photoionization and internal vibrational relaxation (IVR)-not included in the picture of TRSEP, TRSRFD and TRFD-also contribute to the RCS spectra. The obtained rotational constants are in very good agreement with our previous high-resolution TRFD investigation of pCHA, allowing additionally for the unambiguous assignment of the excited state J-type transients. From a linear regression analysis of 25 transient positions (B+C)(')=719.74(53) MHz was calculated, confirming set (II) of our former investigation [C. Riehn, A. Weichert, U. Lommatzsch, M. Zimmermann, and B. Brutschy, J. Chem. Phys. 112, 3650 (2000)].