BIS(PENTAFLUOROPHENYL)CARBONATE, identified by its Chemical Abstracts Service (CAS) number 59483-84-0, stands as a pivotal organic intermediate in the realm of advanced chemical synthesis. This versatile compound is highly valued for its unique chemical structure and reactivity, making it indispensable in the creation of complex molecules and materials across various scientific disciplines. Its robust chemical profile ensures reliability and efficiency in demanding synthetic pathways, underpinning numerous innovative research and industrial applications.

Chemically, BIS(PENTAFLUOROPHENYL)CARBONATE possesses the molecular formula C13F10O3 and a molecular weight of 394.12 g/mol. It typically presents as a white to light yellow powder or crystalline solid, indicative of its high purity and controlled manufacturing processes. The assay for this compound consistently meets or exceeds 97.0% purity, with specialized grades offering even higher levels for the most sensitive reactions. This high level of purity is crucial for ensuring predictable reaction outcomes and minimizing unwanted side reactions in critical synthetic operations.

The physical properties of BIS(PENTAFLUOROPHENYL)CARBONATE contribute to its utility in various laboratory and industrial settings. It features a melting point ranging from 47°C to 50°C and a boiling point of approximately 250°C. Its flash point is recorded at 110°C (230°F), highlighting the importance of proper handling and storage. This compound exhibits excellent solubility in common organic solvents such as chloroform, ethyl acetate, and methylene chloride, facilitating its integration into diverse reaction systems and purification protocols.

One of the primary applications of BIS(PENTAFLUOROPHENYL)CARBONATE is its role as a carbonyl equivalent. This functionality is invaluable in organic synthesis, allowing chemists to introduce carbonyl groups into molecules with precision and efficiency. Furthermore, it is extensively employed in various coupling reactions, serving as a critical building block. Notably, its utility extends to the synthesis of azapeptides, a class of peptides where one or more alpha-carbon atoms of the amino acid residues are replaced by nitrogen atoms, leading to compounds with distinct biological activities and potential therapeutic applications.

Beyond its use in peptide chemistry, BIS(PENTAFLUOROPHENYL)CARBONATE is instrumental in the preparation of specialized cyclic carbonates. An example includes 6,6′-(ethane-1,2-diyl)bis(1,3,6-dioxazocan-2-one), which is a key intermediate in the synthesis of non-isocyanate polyurethanes. These novel polyurethanes offer an environmentally friendly alternative to traditional polyurethanes, which typically rely on toxic isocyanates. Additionally, it aids in the synthesis of coumarin-based aliphatic polycarbonates, such as 5-(4-methylumbelliferyloxycarbonyl)-5-methyl-1,3-dioxan-2-one (MUC), expanding its influence into polymer science and material innovation.

Maintaining the integrity and performance of BIS(PENTAFLUOROPHENYL)CARBONATE necessitates adherence to stringent storage guidelines. For optimal stability and to preserve its high assay, it should be stored in a clean, dry, and cool environment, protected from direct sunlight and moisture. Proper sealing and room temperature storage are recommended to prevent degradation and ensure its readiness for future use in sensitive synthetic procedures.

For those seeking a reliable manufacturer or supplier of high-quality BIS(PENTAFLUOROPHENYL)CARBONATE (CAS 59483-84-0), a comprehensive network of reputable sources ensures widespread availability. When considering to buy or purchase this essential chemical intermediate, it is advisable to inquire about the specific grade and packaging options to meet precise research or production requirements. Competitive price offerings are available for various quantities, catering to both small-scale laboratory needs and larger industrial demands, ensuring that this critical reagent is accessible for diverse synthetic endeavors.