[en] A quantitative interpretation of the molecular satellites of the 6²S-7²P doublet of cesium is given. The calculus, based on the existence of the long-range interaction forces, with approximately R^-3 potential, leads to three molecular states resulting from (7²P-6²S) interaction and two molecular states resulting from (7²P-6²S) interaction, to which electronic transitions from the ground state of the polarization molecule are possible. The potential energy curve was calculated for each molecular state over the whole range of the distance. The theory places the origin of the molecular satellites in the vibrational transitions which take place from the vibrational levels of one ground state to the vibrational levels of more excited molecular states, belonging to the same (7²P-6²S) interaction. (author)