The Chemistry Behind 2-Thiophenecarbonitrile: Synthesis and Properties
Understanding the chemical intricacies of key intermediates is essential for chemists and product formulators. 2-Thiophenecarbonitrile, identified by CAS number 1003-31-2, is a prime example of such a compound, valued for its unique chemical structure and reactivity. This article explores the fundamental chemistry of 2-Thiophenecarbonitrile, covering its synthesis, key properties, and the reasons behind its widespread utility in diverse industrial applications.
2-Thiophenecarbonitrile is a heterocyclic aromatic compound characterized by a five-membered thiophene ring fused with a cyano group at the 2-position. This molecular architecture grants it specific reactivity patterns that are highly sought after in organic synthesis. The electron-withdrawing nature of the nitrile group influences the electron density of the thiophene ring, making it amenable to various electrophilic and nucleophilic substitution reactions. For those looking to buy 2-Thiophenecarbonitrile, understanding these properties is key to successful application.
The synthesis of 2-Thiophenecarbonitrile typically involves established organic chemistry methodologies. While specific proprietary processes vary among manufacturers, common routes often start from thiophene derivatives and employ cyanation reactions. The goal is always to achieve high yields and exceptional purity, often exceeding 99.0%, to meet the stringent requirements of the pharmaceutical, agrochemical, and materials science industries. As a dedicated manufacturer, we employ advanced synthetic techniques to ensure the quality of our 2-Cyanothiophene.
Key physical and chemical properties of 2-Thiophenecarbonitrile include its appearance as a transparent colorless to yellow liquid, a density of approximately 1.172 g/mL at 25°C, and a boiling point around 192°C. It is slightly miscible with water but soluble in many organic solvents. Its flash point is also a critical safety parameter for handling and storage. These properties, along with its reactivity, make it an ideal intermediate for a broad spectrum of applications.
The demand for high-quality CAS 1003-31-2 stems from its crucial role as a building block. In pharmaceuticals, it aids in creating active ingredients; in agrochemicals, it contributes to the efficacy of pesticides; and in materials science, it is used for developing liquid crystals and organic electronics. For companies seeking to purchase this compound, partnering with a reputable supplier like us ensures access to detailed technical data and consistent product quality. We invite you to request a quote and experience the chemical excellence of our 2-Thiophenecarbonitrile.
Perspectives & Insights
Future Origin 2025
“2-Thiophenecarbonitrile is a heterocyclic aromatic compound characterized by a five-membered thiophene ring fused with a cyano group at the 2-position.”
Core Analyst 01
“This molecular architecture grants it specific reactivity patterns that are highly sought after in organic synthesis.”
Silicon Seeker One
“The electron-withdrawing nature of the nitrile group influences the electron density of the thiophene ring, making it amenable to various electrophilic and nucleophilic substitution reactions.”