For research scientists and product formulators, understanding the synthetic utility of key intermediates is fundamental to innovation. (1S)-1-(2-Thienyl)ethanol, identified by CAS number 27948-39-6, stands out as a versatile chiral building block in advanced organic synthesis.

This chiral alcohol, featuring a thiophene ring, is particularly noted for its role in enzymatic reactions. Researchers often leverage lipase-catalyzed acylation to introduce specific functional groups with high stereoselectivity, making (1S)-1-(2-Thienyl)ethanol an ideal substrate for producing enantiomerically pure compounds. This precision is invaluable when developing new pharmaceutical agents, agrochemicals, or specialty materials where stereochemistry dictates biological activity or physical properties.

The molecule's structure allows for a range of transformations. The hydroxyl group can undergo esterification, etherification, or oxidation, while the thiophene ring can participate in electrophilic aromatic substitution or metal-catalyzed cross-coupling reactions. This inherent reactivity makes it a flexible tool for chemists designing complex synthetic pathways.

When you need to buy (1S)-1-(2-Thienyl)ethanol for your lab or pilot-scale production, seeking out a reliable supplier is crucial. Look for companies that specialize in chiral compounds and can guarantee the optical purity and chemical integrity of the product. A dedicated chemical manufacturer in China can often provide the high-quality material required, along with competitive pricing and timely delivery, supporting your research and development timelines.

Whether you are synthesizing novel drug candidates, developing advanced materials, or exploring new catalytic processes, (1S)-1-(2-Thienyl)ethanol is a building block worth considering. Its contribution to stereoselective synthesis underscores its importance in modern organic chemistry.