In the realm of organic chemistry, asymmetric synthesis is a cornerstone for creating enantiomerically pure compounds, vital for pharmaceuticals, agrochemicals, and advanced materials. At the heart of many such syntheses lies the strategic use of chiral building blocks. (R)-1-Phenylethanol (CAS 1517-69-7) is a versatile and widely employed chiral alcohol that serves as an excellent starting material or intermediate in these complex molecular constructions.

The significance of (R)-1-Phenylethanol in asymmetric synthesis stems from its defined stereochemistry. This specific enantiomer allows chemists to introduce chirality into target molecules with a high degree of control. Researchers often utilize it in reactions such as esterifications, etherifications, and oxidations, where the chiral center is preserved or transferred to a new molecule. The ability to reliably obtain this specific enantiomer is crucial for reproducible research and industrial scale-up.

For R&D scientists embarking on projects involving asymmetric synthesis, sourcing a high-quality source of (R)-1-Phenylethanol is paramount. When looking to buy this crucial building block, it is advisable to consult with manufacturers and suppliers who specialize in chiral compounds. These suppliers often provide detailed specifications, including high optical purity values (e.g., [α]22/D +44.0°) and accompanying certificates of analysis. Engaging with a manufacturer based in China can often provide cost-effective procurement options without sacrificing quality.

The physical properties of (R)-1-Phenylethanol, such as its liquid form and boiling point (88-89 °C at 10 mmHg), facilitate its handling and use in standard laboratory and industrial reactors. Its compatibility with a range of solvents further enhances its utility in diverse synthetic pathways. Researchers should always refer to the material safety data sheet (MSDS) provided by the supplier for comprehensive handling and safety information.

When seeking to purchase (R)-1-Phenylethanol for your research, consider its role in producing other chiral intermediates or functional molecules. Its phenyl group and hydroxyl functionality offer reactive sites for a multitude of chemical transformations. Furthermore, its accessibility as a commercial product makes it an attractive option for both academic exploration and industrial application development. Requesting a price quote from a reliable chemical supplier is a key step in planning your synthetic strategy.

In conclusion, (R)-1-Phenylethanol is an invaluable tool for chemists engaged in asymmetric synthesis. Its defined chirality, versatile reactivity, and commercial availability make it a preferred choice for constructing complex chiral molecules. By partnering with reputable manufacturers and understanding its chemical attributes, scientists can effectively leverage this building block to drive innovation in chemical synthesis.