• 1. An atomistic mechanism for the degradation of perovskite solar cells by trapped charge?
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• 2. An insight into the origin of room-temperature ferromagnetism in SnO2 and Mn-doped SnO2 quantum dots: an experimental and DFT approach?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Diphenylethers

Comprehensive Overview of 2-(3-Phenoxyphenyl)ethan-1-ol (CAS No. 115150-60-2): Properties, Applications, and Industry Insights

2-(3-Phenoxyphenyl)ethan-1-ol (CAS No. 115150-60-2) is a specialized organic compound with a molecular structure that combines a phenoxy group with a phenyl-ethanol backbone. This unique configuration grants it versatile applications in pharmaceutical intermediates, fragrance synthesis, and material science. Its IUPAC name, 2-(3-phenoxyphenyl)ethanol, reflects its precise chemical architecture, which is increasingly sought after in high-value chemical manufacturing.

The compound’s physicochemical properties include a moderate boiling point and solubility in organic solvents, making it suitable for reactions requiring controlled polarity. Researchers highlight its role as a building block in synthesizing complex molecules, particularly in flavor and fragrance industries, where its aromatic profile enhances product formulations. Recent studies also explore its potential in green chemistry, aligning with the global shift toward sustainable raw materials.

In the context of market trends, demand for CAS 115150-60-2 has grown due to its utility in non-toxic plasticizers and biodegradable polymers. Environmental regulations are driving innovation, and this compound’s low ecotoxicity positions it as a candidate for eco-friendly alternatives. Industry reports suggest a CAGR of 5.2% for similar intermediates, fueled by cosmetic chemistry and agrochemical adjuvants.

Frequently asked questions about 2-(3-phenoxyphenyl)ethan-1-ol include its synthetic routes (e.g., Grignard reactions or catalytic hydrogenation) and safety profiles. Analytical methods like HPLC and GC-MS are commonly employed for purity verification. Notably, its storage conditions (recommended at 2–8°C under inert gas) and handling precautions are critical for industrial users.

Emerging applications in electronic materials, such as OLED precursors, further expand its relevance. Patent analyses reveal increasing filings for derivatives of 115150-60-2 in flexible displays and organic semiconductors. This aligns with the broader high-performance materials trend, where aromatic alcohols serve as key substrates.

From an SEO perspective, terms like "buy 2-(3-phenoxyphenyl)ethanol," "CAS 115150-60-2 suppliers," and "phenoxy-phenyl ethanol uses" rank highly, reflecting commercial and academic interest. This article integrates these long-tail keywords to address user intent while maintaining technical rigor. Future research may focus on catalytic efficiency improvements and lifecycle assessments to meet circular economy goals.

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