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Comprehensive Overview of (2R)-2-aminohex-3-en-1-ol (CAS No. 2227799-50-8)

(2R)-2-aminohex-3-en-1-ol is a chiral amino alcohol with the CAS number 2227799-50-8. This compound has garnered significant attention in the field of organic chemistry due to its unique structural features and potential applications in pharmaceuticals, agrochemicals, and specialty chemicals. The presence of both amino and hydroxyl functional groups, along with a double bond in the hexenyl chain, makes it a versatile intermediate for synthesizing more complex molecules.

The chiral center at the second carbon atom (denoted by the (2R) configuration) is particularly noteworthy, as it imparts stereoselectivity to reactions involving this compound. Researchers are increasingly interested in enantiomerically pure compounds like (2R)-2-aminohex-3-en-1-ol due to their role in asymmetric synthesis and drug development. The demand for such intermediates has surged in recent years, driven by the growing emphasis on green chemistry and sustainable manufacturing processes.

One of the most common questions about (2R)-2-aminohex-3-en-1-ol is its synthesis. The compound can be prepared via several routes, including asymmetric hydrogenation of corresponding enamines or enzymatic resolution of racemic mixtures. Recent advancements in biocatalysis have made it possible to produce this compound with high enantiomeric excess, which is crucial for pharmaceutical applications. Additionally, its solubility in polar solvents like water and ethanol makes it suitable for various reaction conditions.

The applications of (2R)-2-aminohex-3-en-1-ol are diverse. In the pharmaceutical industry, it serves as a building block for active pharmaceutical ingredients (APIs) targeting neurological and metabolic disorders. Its structural motif is found in several drug candidates undergoing clinical trials. Another hot topic is its use in agrochemicals, where it contributes to the development of eco-friendly pesticides and herbicides. The compound's ability to act as a ligand in catalysis also makes it valuable in industrial chemical processes.

From a market perspective, the global demand for chiral amino alcohols like (2R)-2-aminohex-3-en-1-ol is on the rise. Companies specializing in fine chemicals and custom synthesis are investing heavily in scalable production methods to meet this demand. The compound's stability under standard storage conditions and its compatibility with various reaction media further enhance its commercial viability. Researchers are also exploring its potential in material science, particularly in the design of polymers with tailored properties.

For those searching for "buy (2R)-2-aminohex-3-en-1-ol" or "suppliers of CAS 2227799-50-8," it's essential to verify the purity and enantiomeric excess of the product. Reputable suppliers typically provide detailed analytical data, including HPLC or GC-MS reports, to ensure quality. The compound is often available in research quantities, but bulk procurement may require custom synthesis agreements. Pricing varies depending on the scale and purity requirements.

In conclusion, (2R)-2-aminohex-3-en-1-ol (CAS No. 2227799-50-8) is a promising chiral building block with wide-ranging applications. Its role in drug discovery, catalysis, and sustainable chemistry makes it a compound of significant interest to both academia and industry. As research continues to uncover new uses for this molecule, its importance in the chemical landscape is expected to grow further.

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