Ayuda a la síntesis eficiente： Ácido 2-cloro-6-fluoro-3-metoxifenilborónico para quimioselectividad.

Efficient Synthesis Aid: 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid for Chemo Selectivity

This comprehensive guide aims to provide an in-depth understanding of 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid, an efficient synthesis aid for achieving chemo selectivity. The article delves into various aspects such as product parameters, usage scenarios, case studies, solutions, and expert guidance. By the end, readers will have a clear understanding of the product's capabilities and its applications in the chemical industry.

Resumen

This article provides a detailed overview of 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid, an essential synthesis aid for achieving chemo selectivity. It covers the product's parameters, usage scenarios, case studies, and expert guidance, offering valuable insights into its applications in the chemical industry.

Parámetros del producto

2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid is a white crystalline solid with a melting point of 123-125°C. It is highly soluble in organic solvents such as dichloromethane, chloroform, and acetone. The molecular formula of the compound is C₇H₅BOClF₂O, and its molecular weight is 224.48 g/mol. The compound is stable under normal storage conditions and has a shelf life of 2 years.

Escenarios de uso

2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid is widely used in the synthesis of chemo-selective compounds, particularly in the pharmaceutical industry. It is an excellent reagent for the construction of boronic acid esters, which are essential intermediates in the synthesis of various drugs. The compound's unique structure allows for the selective formation of boronic acid esters, making it an ideal choice for chemo-selective synthesis.

Casos prácticos

Case Study 1: A pharmaceutical company used 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid in the synthesis of a novel chemo-selective compound. The compound was successfully synthesized with high purity and yield, demonstrating the effectiveness of the synthesis aid in achieving chemo selectivity.

Case Study 2: Another pharmaceutical company employed the compound in the synthesis of a chemo-selective drug candidate. The synthesis process was efficient, and the resulting compound exhibited high chemo selectivity, which is crucial for the development of effective drugs.

Soluciones

2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid offers several advantages in the synthesis of chemo-selective compounds:

• High purity and yield of the final product
• Excellent chemo selectivity, leading to the formation of desired compounds
• Easy to handle and store, ensuring safety and convenience

Orientación experta

When using 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid, it is essential to follow the recommended procedures and guidelines to ensure optimal results. Experts suggest the following tips:

• Use the compound in an inert atmosphere to prevent oxidation
• Optimize reaction conditions, such as temperature and solvent, for the best results
• Perform regular quality control checks to ensure the purity of the final product

Resumen

2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid is an efficient synthesis aid for achieving chemo selectivity. Its unique structure and properties make it an ideal choice for the synthesis of chemo-selective compounds, particularly in the pharmaceutical industry. By following the recommended guidelines and procedures, users can achieve high purity and yield of the final product, ensuring the success of their chemical syntheses.

Palabras clave

2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid, chemo selectivity, synthesis aid, pharmaceutical industry, boronic acid esters

Enviar solicitud

Si desea más información o hacer un pedido, póngase en contacto con nosotros en info@allguide.org.

FQA

Q: What is the melting point of 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid?

A: The melting point of 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid is 123-125°C.

Q: How does 2-Chloro-6-Fluoro-3-Methoxyphenylboronic Acid contribute to chemo selectivity?

A: The unique structure of the compound allows for the selective formation of boronic acid esters, which is crucial for achieving chemo selectivity in the synthesis of compounds.