In the intricate world of organic chemistry and pharmaceutical synthesis, understanding the precise properties of chemical intermediates is crucial for success. Boc-O-benzyl-L-tyrosine, a key derivative of tyrosine, is one such compound whose unique chemical characteristics make it invaluable for advanced synthesis projects. This article, brought to you by NINGBO INNO PHARMCHEM CO.,LTD., aims to illuminate these properties and their impact on various applications.

Boc-O-benzyl-L-tyrosine, with CAS number 19391-35-6, is distinguished by its strategically placed protecting groups. The tert-butoxycarbonyl (Boc) group attached to the alpha-amino nitrogen offers acid-labile protection, meaning it can be efficiently removed by mild acidic treatment. This feature is essential in peptide synthesis for controlled coupling of amino acids. Concurrently, the benzyl ether protecting the hydroxyl group on the tyrosine side chain provides stability under acidic conditions but can be cleaved under reductive conditions, such as catalytic hydrogenation. This orthogonal protection strategy is a hallmark of effective amino acid derivative chemistry and is central to the utility of Boc-O-benzyl-L-tyrosine.

The solubility profile of Boc-O-benzyl-L-tyrosine typically includes good solubility in common organic solvents like dichloromethane, ethyl acetate, and dimethylformamide (DMF), which are frequently used in synthesis. Its solid form, often a white powder, ensures ease of handling and accurate weighing for reactions. The purity of the compound is also a critical chemical property; high-purity Boc-O-benzyl-L-tyrosine, such as that supplied by NINGBO INNO PHARMCHEM CO.,LTD., guarantees predictable reactivity and minimizes the formation of unwanted byproducts. When you buy N-Boc-O-benzyl-L-tyrosine, you are investing in a precisely engineered molecule designed for specific chemical transformations.

These chemical properties directly translate into its widespread use. In N-Boc-O-benzyl-L-tyrosine peptide synthesis, the acid-labile Boc group allows for sequential amino acid addition without affecting the benzyl protection on the tyrosine side chain. This differential lability is key to building complex peptide sequences with high fidelity. Furthermore, its role as a pharmaceutical intermediate means that the stability and reactivity of Boc-O-benzyl-L-tyrosine are thoroughly vetted for large-scale manufacturing processes. The price of N-Boc-O-benzyl-L-tyrosine reflects the complexity of its synthesis and purification.

NINGBO INNO PHARMCHEM CO.,LTD. is a leading supplier of high-quality Boc-O-benzyl-L-tyrosine. We understand that the success of your advanced synthesis projects hinges on the quality of your starting materials. Our commitment to excellence ensures that our CAS 19391-35-6 amino acid derivative meets the rigorous demands of chemical synthesis. Trust NINGBO INNO PHARMCHEM CO.,LTD. to provide the reliable Boc-O-benzyl-L-tyrosine you need for your groundbreaking research and development.