Revolutionize Your Synthesis with Furo[2,3-c]pyridin-3(2H)-one – Efficient Solutions for Complex Reactions
Resumen
This article provides a comprehensive guide on how to revolutionize your synthesis with Furo[2,3-c]pyridin-3(2H)-one, an efficient solution for complex reactions. It covers various aspects such as product parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs to help users make informed decisions.
Introducción
Furo[2,3-c]pyridin-3(2H)-one is a versatile compound widely used in organic synthesis. It has gained significant attention due to its unique structure and ability to facilitate complex reactions. This guide aims to provide users with a detailed understanding of this product, its applications, and how it can enhance their synthesis processes.
Parámetros del producto
Furo[2,3-c]pyridin-3(2H)-one is a white crystalline solid with a melting point of 123-125°C. It is soluble in common organic solvents such as methanol, ethanol, and chloroform. The molecular formula of this compound is C10H6N2O, and its molecular weight is 166.18 g/mol. The following table provides a summary of its physical and chemical properties:
Propiedad | Valor |
---|---|
Fórmula molecular | C10H6N2O |
Peso molecular | 166,18 g/mol |
Punto de fusión | 123-125°C |
Solubilidad | Soluble en metanol, etanol, cloroformo |
Escenarios de uso
Furo[2,3-c]pyridin-3(2H)-one is a versatile building block in organic synthesis, suitable for various applications. Some common usage scenarios include:
- Síntesis de compuestos heterocíclicos
- Construction of bioactive molecules
- Development of novel pharmaceuticals
Casos prácticos
Here are two case studies showcasing the use of Furo[2,3-c]pyridin-3(2H)-one in complex reactions:
Caso práctico 1: Síntesis de un compuesto heterocíclico
Company A used Furo[2,3-c]pyridin-3(2H)-one as a key intermediate in the synthesis of a heterocyclic compound. The reaction involved a cyclization process, which was facilitated by the unique structure of the compound. The resulting heterocyclic compound exhibited promising biological activity, leading to the development of a novel drug candidate.
Case Study 2: Construction of a Bioactive Molecule
Company B employed Furo[2,3-c]pyridin-3(2H)-one in the construction of a bioactive molecule. The compound was used as a building block in a multistep synthesis, which involved various transformations such as cyclization, substitution, and oxidation. The final bioactive molecule demonstrated significant activity against a specific target, paving the way for further research and development.
Soluciones
Revolutionize Your Synthesis with Furo[2,3-c]pyridin-3(2H)-one offers several solutions to enhance your synthesis processes:
- Improved reaction efficiency
- Enhanced selectivity
- Reducción del tiempo de reacción
Orientación experta
Our team of experts is available to provide guidance on the use of Furo[2,3-c]pyridin-3(2H)-one in your synthesis processes. We can help you optimize reaction conditions, select appropriate solvents, and identify the best catalysts for your specific application.
Preguntas frecuentes
Q: Is Furo[2,3-c]pyridin-3(2H)-one safe to handle?
A: Yes, Furo[2,3-c]pyridin-3(2H)-one is considered safe to handle when proper precautions are taken. It is important to wear appropriate personal protective equipment (PPE) and follow good laboratory practices.
Q: Can Furo[2,3-c]pyridin-3(2H)-one be used in large-scale synthesis?
A: Yes, Furo[2,3-c]pyridin-3(2H)-one is suitable for large-scale synthesis. It has been used in various industrial applications, demonstrating its scalability and reliability.
Conclusión
Revolutionize Your Synthesis with Furo[2,3-c]pyridin-3(2H)-one is an efficient solution for complex reactions in organic synthesis. Its unique structure and versatility make it an excellent choice for various applications, including the synthesis of heterocyclic compounds, bioactive molecules, and novel pharmaceuticals. By following this guide, users can make informed decisions and optimize their synthesis processes.
Palabras clave
Furo[2,3-c]pyridin-3(2H)-one, organic synthesis, heterocyclic compounds, bioactive molecules, pharmaceuticals, reaction efficiency, selectivity, catalysts
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