We present the rational design and synthesis of an innovative tricolor photochromic switch featuring a unique molecular architecture combining an E-tetra-arylethene core with dual benzophenone moieties. The system demonstrates exceptional bidirectional photoresponsive behavior, achieving near-quantitative E-Z isomerization (yields >99%) and efficient photoinduced cyclization/cycloreversion reactions in tetrahydrofuran solution. This sophisticated photochromic interplay enables precise tricolor modulation through controlled light irradiation. Notably, the system exhibits light-regulated thermal reversibility, offering unprecedented control over its relaxation dynamics. The photochromic performance remains robust across different matrices, including PMMA polymer films and cellulose filter paper substrates. This multi-addressable color-switching platform demonstrates promising potential for advanced optical applications, particularly in dynamic information encryption systems and multi-level anti-counterfeiting technologies.