Organic synthesis is the bedrock of chemical innovation, enabling the creation of molecules that drive progress in pharmaceuticals, materials science, and beyond. At the heart of many synthetic endeavors are versatile intermediates like 1-(4-Hydroxypiperidin-1-yl)ethanone, known by its CAS number 4045-22-1. This compound, characterized by its unique structure incorporating a hydroxyl-substituted piperidine ring and an ethanone moiety, offers chemists a powerful tool for building complex molecular architectures.

The utility of 1-(4-Hydroxypiperidin-1-yl)ethanone in organic synthesis lies in its inherent reactivity and the strategic placement of its functional groups. The hydroxyl group can be readily derivatized through esterification, etherification, or oxidation, while the piperidine nitrogen can participate in various coupling or substitution reactions. The ketone carbonyl offers further opportunities for transformations such as reduction to an alcohol or nucleophilic addition. These versatile reaction pathways make it an ideal starting material for synthesizing a wide range of target molecules, from pharmaceuticals to agrochemicals. The accessibility of this compound, often available for purchase from specialized chemical suppliers, ensures that researchers can readily incorporate it into their synthetic strategies. The competitive price points for quality 1-(4-hydroxypiperidin-1-yl)ethanone are also a significant factor in its widespread adoption in research labs.

One of the key areas where 1-(4-Hydroxypiperidin-1-yl)ethanone plays a vital role is in the development of pharmaceutical intermediates. Its structure is amenable to being incorporated into molecules designed to interact with biological targets. For instance, researchers have explored derivatives of this compound for their potential antibacterial properties, showcasing its contribution to medicinal chemistry research. The ability to reliably synthesize and modify this intermediate is crucial for the systematic exploration of structure-activity relationships, a fundamental aspect of drug discovery. The consistent quality offered by manufacturers of CAS 4045-22-1 is essential for reproducible research outcomes.

Furthermore, advancements in synthetic methodologies continue to unlock new ways to utilize 1-(4-Hydroxypiperidin-1-yl)ethanone. Modern techniques such as multicomponent reactions and transition-metal-catalyzed couplings can be employed to efficiently assemble complex structures starting from this intermediate. The focus on greener chemistry principles also drives the development of more sustainable synthesis routes for such compounds, minimizing waste and improving atom economy. The availability of 1-(4-hydroxypiperidin-1-yl)ethanone at competitive prices allows research institutions and chemical companies to invest in these advanced synthetic approaches, pushing the boundaries of what is achievable in molecular design.

In conclusion, 1-(4-Hydroxypiperidin-1-yl)ethanone (CAS 4045-22-1) is a cornerstone intermediate in modern organic synthesis. Its inherent chemical versatility, coupled with its pivotal role in developing pharmaceutical intermediates and facilitating innovative research, underscores its importance. As chemists continue to explore new molecular frontiers, this compound remains an essential tool, driving progress and innovation across the chemical sciences.