Sourcing High-Purity Methyl 2-Cyclopropyl-4-(4-Fluorophenyl)-3-Quinolinecarboxylate for Pharmaceutical R&D
In the demanding field of pharmaceutical research and development (R&D), the quality and availability of chemical intermediates are critical determinants of success. Methyl 2-Cyclopropyl-4-(4-Fluorophenyl)-3-Quinolinecarboxylate, bearing the CAS number 121659-86-7, is one such compound that plays a pivotal role, particularly in the synthesis of cardiovascular drugs like Pitavastatin. This article addresses the importance of sourcing this high-purity intermediate and the factors that govern its procurement for pharmaceutical applications.
Methyl 2-Cyclopropyl-4-(4-Fluorophenyl)-3-Quinolinecarboxylate is a complex organic molecule with the chemical formula C20H16FNO2 and a molecular weight of 321.34. It is typically presented as a white solid, indicating a well-purified compound essential for sensitive pharmaceutical syntheses. The molecule's structure is characterized by a quinoline ring system, which is a common pharmacophore in many medicinal compounds, further functionalized with a cyclopropyl group and a fluorophenyl moiety. This specific combination of structural elements makes it an ideal building block for targeted drug synthesis. The 'fluorophenyl compound' aspect, in particular, often contributes to improved pharmacokinetic properties in the final drug product.
The primary application for this compound is its role as a key 'pitavastatin intermediate'. The synthesis of Pitavastatin, a widely prescribed statin, requires multiple steps, and the reliability of each intermediate is crucial. Therefore, researchers and manufacturers frequently engage in searches for reliable 'methyl 2-cyclopropyl-4-(4-fluorophenyl)-3-quinolinecarboxylate suppliers'. The purity of the intermediate directly affects the quality of the final API, influencing its efficacy, safety profile, and regulatory compliance. Sourcing from reputable 'methyl 2-cyclopropyl-4-(4-fluorophenyl)-3-quinolinecarboxylate suppliers' who adhere to stringent quality control measures is paramount.
The process of 'pitavastatin intermediate synthesis' demands intermediates that meet rigorous specifications. Methyl 2-Cyclopropyl-4-(4-Fluorophenyl)-3-Quinolinecarboxylate, being a crucial 'pharmaceutical intermediate', must consistently exhibit high purity and well-defined chemical characteristics. Its structural features, such as the quinoline backbone and the ester group, are strategically utilized in multi-step synthesis pathways. The ability to accurately 'buy methyl 2-cyclopropyl-4-(4-fluorophenyl)-3-quinolinecarboxylate' with guaranteed quality empowers R&D teams to proceed with their projects without compromising on the integrity of their research.
Companies like NINGBO INNO PHARMCHEM CO.,LTD. contribute significantly to the pharmaceutical supply chain by ensuring the availability of such specialized chemicals. Their dedication to producing high-quality chemical compounds is essential for the advancement of drug discovery and manufacturing. For any entity involved in pharmaceutical R&D, understanding the properties and sourcing challenges of compounds like this 'carboxylic acid methyl ester intermediate' is fundamental to achieving project goals.
In summary, Methyl 2-Cyclopropyl-4-(4-Fluorophenyl)-3-Quinolinecarboxylate (CAS 121659-86-7) is an indispensable component in the pharmaceutical industry. Its role as a high-purity intermediate in the synthesis of essential medications highlights the importance of careful sourcing and quality control. As pharmaceutical science progresses, the demand for such precisely engineered chemical building blocks will continue to grow, solidifying their place at the forefront of medical innovation.
Perspectives & Insights
Alpha Spark Labs
“The synthesis of Pitavastatin, a widely prescribed statin, requires multiple steps, and the reliability of each intermediate is crucial.”
Future Pioneer 88
“Therefore, researchers and manufacturers frequently engage in searches for reliable 'methyl 2-cyclopropyl-4-(4-fluorophenyl)-3-quinolinecarboxylate suppliers'.”
Core Explorer Pro
“The purity of the intermediate directly affects the quality of the final API, influencing its efficacy, safety profile, and regulatory compliance.”