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The Chemical Profile of (S)-1-(4-Bromophenyl)Ethanol for R&D Scientists

For R&D scientists engaged in organic synthesis and drug discovery, understanding the chemical properties and synthetic utility of key intermediates is fundamental. (S)-1-(4-Bromophenyl)Ethanol, identified by CAS 100760-04-1, is a prime example of such a versatile building block. This article delves into its chemical profile and highlights why it is an indispensable compound for innovative research, brought to you by a leading manufacturer of fine chemicals.

The molecular structure of (S)-1-(4-Bromophenyl)Ethanol (C8H9BrO) is key to its reactivity. It features a benzene ring substituted with a bromine atom at the para position and an ethyl group bearing a hydroxyl moiety at the alpha position, with a defined stereochemistry at the chiral center (S configuration). The presence of the bromine atom makes it an excellent substrate for various palladium-catalyzed cross-coupling reactions, such as Suzuki, Heck, and Sonogashira couplings, enabling the introduction of complex organic fragments. The secondary alcohol group can be readily oxidized to a ketone or esterified, further expanding its synthetic potential.

As a chiral intermediate, (S)-1-(4-Bromophenyl)Ethanol is particularly valuable in asymmetric synthesis, where the precise three-dimensional arrangement of atoms is critical for biological activity. Pharmaceutical scientists often utilize this compound to construct enantiomerically pure drug candidates, ensuring optimal efficacy and minimizing off-target effects. Researchers aiming to buy this compound can rely on us for its consistent enantiomeric purity, a testament to our manufacturing expertise and stringent quality control protocols. Sourcing from a reliable supplier ensures that your research is built upon a foundation of high-quality reagents.

The physical properties of (S)-1-(4-Bromophenyl)Ethanol are also noteworthy. Typically appearing as a colorless liquid with a density of approximately 1.322 g/mL at 25°C and a refractive index of n20/D 1.570, its handling and reaction conditions can be optimized based on these parameters. Proper storage, as recommended by manufacturers, usually involves keeping it in a cool, dry, and well-ventilated area away from heat and light, ensuring its stability and reactivity over time.

For R&D scientists exploring new synthetic routes or developing novel compounds, (S)-1-(4-Bromophenyl)Ethanol is an excellent starting material. Its brominated aromatic ring and chiral alcohol function provide a rich platform for chemical exploration. We, as a professional manufacturer and supplier, are committed to facilitating your research endeavors by providing this essential chemical with guaranteed quality and accessibility. When you need to buy this versatile building block, consider our comprehensive offerings and expert support.

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