Catalytic CO2 hydrogenation to methanol has received considerable attention its all effective Way to utilize CO2. In this paper, density functional theory was employed to investigate the methanol synthesis from CO, and H-2 on a Mo6S8 cluster. The Mo6S8 cluster is the structural building block of the Chevrel phase of molybdenum sulfide, and has a cagelike structure With all octahedral Mo-6 metallic core. Our calculations indicate that the preferred catalytic pathway for methanol synthesis on the Mo6S8 Cluster is very different from that of bulklike MoS2, MoS2 promotes the C-O scission of HxCO intermediated, and therefore, only hydrocarbons are produced. The lower S/Mo ratio for the cluster compared to stoichiometric MoS2 might be expected to lead to higher activity because more low-coordinated Mo sites are available for reaction. However, our results show that the Mo6S8 cluster is not as reactive as bulk MoS2 because it is unable to break the C-O bond of HxCO intermediates and therefore cannot produce hydrocarbons. Yet, the Mo6S8 cluster is predicted to have moderate activity for converting CO2 and H-2 to methanol. The overall reaction pathway involves the reverse water-gas shift reaction (CO2 + H-2 -> CO + H2O), followed by CO hydrogenation via HCO (CO + 2H(2) -> CH3OH) to form methanol. The rate-limiting step is CO hydrogenation to the HCO with a calculated barrier of +1 eV. This barrier is much lower than that calculated for a comparably sized Cu nanoparticle. which is the prototypical metal catalyst used for methanol synthesis from syngas (CO + H-2). Both the Mo and S sites participate in the reaction with CO2, CO. and CHxO preferentially binding to the Mo sites, whereas S atoms facilitate bond cleavage by forming relatively Strong S-H bonds. Our study reveals that the unexpected activity of the Mo6S8 cluster is the result of the interplay between shifts ill the Mo cl-band and S p-band and its unique cagelike geometry.