Exploring the Chemistry of 2-Acetylthiophene: Synthesis and Properties
The foundation of chemical innovation often rests on understanding the core properties and synthesis routes of key chemical intermediates. 2-Acetylthiophene, bearing the CAS number 88-15-3, is a prime example of such a compound. Its structure, combining a thiophene ring with an acetyl group, grants it unique chemical characteristics that are exploited in a multitude of applications. NINGBO INNO PHARMCHEM CO.,LTD. is committed to providing high-quality 2-Acetylthiophene and sharing knowledge about its synthesis and properties.
The journey to understand 2-Acetylthiophene begins with its synthesis. While various methods exist, a common approach involves the Friedel-Crafts acylation of thiophene. This reaction, utilizing acetyl chloride or acetic anhydride in the presence of a Lewis acid catalyst like aluminum chloride, effectively attaches the acetyl group to the thiophene ring, typically at the 2-position. Understanding the '2-acetylthiophene synthesis' pathways is crucial for efficient and high-yield production.
The resulting compound, 2-Acetylthiophene, is characterized by its physical form – a clear, colorless to pale yellow liquid at room temperature. It possesses a distinct aroma described as sulfurous, nutty, and hazelnut-like, which contributes to its use in the fragrance industry. The purity of the compound is a critical parameter, with manufacturers typically aiming for levels of 98% or higher, often verified by Gas Chromatography (GC). Examining the 'CAS 88-15-3 chemical properties' reveals these vital specifications.
Further insights into its behavior can be found by looking at its solubility and reactivity. 2-Acetylthiophene is generally insoluble in water but soluble in many common organic solvents, which is advantageous for its use in various reaction media. Its molecular weight is approximately 126.18 g/mol, and its molecular formula is C6H6OS. These fundamental 'chemical properties of CAS 88-15-3' are essential for chemists designing synthetic routes.
The reactivity of the carbonyl group and the thiophene ring allows 2-Acetylthiophene to participate in a wide range of organic transformations. This makes it a versatile 'chemical intermediate' for creating more complex molecular structures. Whether it's for developing novel pharmaceuticals or specialized industrial chemicals, the controlled reactivity of 2-Acetylthiophene is highly prized.
NINGBO INNO PHARMCHEM CO.,LTD. ensures that the 'buy 2-Acetylthiophene' process is straightforward for researchers and manufacturers alike. By focusing on consistent product quality and providing detailed technical information, we aim to be a reliable partner in advancing chemical science and industry. Our commitment to understanding and optimizing the 'uses of Methyl 2-thienyl ketone' ensures that our clients receive a product that meets the highest standards for their specific applications.
Perspectives & Insights
Agile Reader One
“The purity of the compound is a critical parameter, with manufacturers typically aiming for levels of 98% or higher, often verified by Gas Chromatography (GC).”
Logic Vision Labs
“Examining the 'CAS 88-15-3 chemical properties' reveals these vital specifications.”
Molecule Origin 88
“Further insights into its behavior can be found by looking at its solubility and reactivity.”