(1R,2R)-(-)-trans-cyclohexane-1,2-dicarboxylicacid CAS:46022-05-3

(1R,2R)-(-)-trans-Cyclohexane-1,2-dicarboxylic acid finds diverse applications in pharmaceutical research, polymer science, and materials engineering. One of its primary uses is as a chiral auxiliary for asymmetric synthesis, enantioselective catalysis, and stereochemical control in organic reactions. Chemists utilize this compound to introduce chiral motifs into molecules, enabling the preparation of enantiomerically pure compounds, pharmaceutical intermediates, and advanced materials with specific stereochemistry required for drug discovery, materials design, and chemical transformations. In addition to its role as a chiral building block, (1R,2R)-(-)-trans-Cyclohexane-1,2-dicarboxylic acid is employed in polymerization processes, resin formulations, and copolymer modifications. Its unique structure and reactivity facilitate the creation of specialty polymers, functional materials, and cross-linked networks with tailored properties, mechanical strength, and thermal stability for industrial applications requiring high-performance materials, adhesives, and coatings with enhanced characteristics and specific functionalities. Furthermore, this compound serves as a reagent in academic research, chemical investigations, and synthetic methodologies. Scientists leverage its stereochemistry, conformational rigidity, and functional groups to probe molecular interactions, study reaction mechanisms, and explore new pathways in organic chemistry, catalysis, and materials science, contributing to advancements in chemical synthesis, stereochemical control, and structural diversity in molecular design. Moreover, (1R,2R)-(-)-trans-Cyclohexane-1,2-dicarboxylic acid is utilized in medicinal chemistry for designing enzyme inhibitors, drug conjugates, and pharmacophores. Its role in drug development, molecular recognition, and bioactive compound synthesis enables the creation of novel pharmaceutical agents, therapeutic candidates, and drug delivery systems with improved efficacy, target specificity, and biological activity, supporting advancements in pharmaceutical sciences, therapeutic interventions, and healthcare innovations. Overall, (1R,2R)-(-)-trans-Cyclohexane-1,2-dicarboxylic acid plays a crucial role in chiral synthesis, material design, chemical research, and pharmaceutical investigations. Its contributions to stereochemistry, polymer science, drug discovery, and scientific explorations underscore its versatility and significance in advancing knowledge, technology, and chemical applications across diverse fields of chemistry, pharmaceutical sciences, polymer engineering, and scientific endeavors, demonstrating its importance in driving innovation, discoveries, and practical solutions for societal needs.