Molecular ferroelectrics as alternatives to the conventional inorganic ferroelectrics have been greatly developed in past decades; many of these have been discovered and designed through various chemical means due to their structural adjustability. However, it is still a huge challenge to obtain high (above room temperature) Curie temperature (T-c) molecular ferroelectrics to meet the application requirements. Here, we present a new organic-inorganic hybrid molecular ferroelectric, [cyclopentylammonium](2)CdBr4 (1), showing a moderate above-room-temperature T-c of 340.3 K. The mechanism of the ferroelectric phase transition from Pnam to Pna2(1) in 1 is ascribed to the order-disorder transition of r both the organic cations and inorganic anions, affording a spontaneous polarization of 0.57 mu C/cm(2) for the ferroelectric phase. Using piezoresponse force microscopy (PFM), we clearly observed the antiparallel 180 degrees stripe domains and realized the polarization switching, unambiguously establishing the existence of room-temperature ferroelectricity in the thin film. These attributes make it attractive for use in flexible devices, soft robotics, biomedical devices, and other applications.