Auxiliar de síntese eficiente: Ácido 3-Carboxi-2-Fluorofenilborónico para soluções de quimio-seletividade

Efficient Synthesis Aid: 3-Carboxy-2-Fluorophenylboronic Acid for Chemo Selectivity Solutions

This comprehensive guide aims to provide an in-depth understanding of 3-Carboxy-2-Fluorophenylboronic Acid, an efficient synthesis aid for addressing chemo selectivity challenges in chemical reactions. By analyzing user search intent on Google, we have crafted this guide to offer practical solutions and insights into the usage of this compound.

Resumo

This article offers a detailed overview of 3-Carboxy-2-Fluorophenylboronic Acid, a valuable synthesis aid for achieving chemo selectivity in chemical reactions. It covers various aspects, including product parameters, usage scenarios, case studies, solutions, and expert guidance. The guide aims to assist users in understanding the benefits and applications of this compound, providing a comprehensive solution for chemo selectivity challenges.

Parâmetros do produto

3-Carboxy-2-Fluorophenylboronic Acid is a white to off-white crystalline solid with a melting point of 135-137°C. It is highly soluble in polar solvents such as water, methanol, and ethanol. The compound has a molecular formula of C7H5BF2CO2H and a molecular weight of 194.99 g/mol. The following table provides a summary of the key physical and chemical properties of the compound:

Imóveis Valor
Fórmula molecular C7H5BF2CO2H
Peso molecular 194,99 g/mol
Ponto de fusão 135-137°C
Solubilidade Água, Metanol, Etanol

Cenários de utilização

3-Carboxy-2-Fluorophenylboronic Acid is widely used in various chemical reactions, particularly those requiring chemo selectivity. Some common usage scenarios include:

  • As a chemo-selective reagent in Suzuki coupling reactions
  • For the synthesis of biologically active compounds
  • In the preparation of pharmaceutical intermediates

Estudos de caso

Here are two case studies showcasing the application of 3-Carboxy-2-Fluorophenylboronic Acid in real-world scenarios:

Case Study 1: Suzuki Coupling Reaction

Company A, a leading pharmaceutical manufacturer, faced challenges in achieving chemo selectivity during the synthesis of a key intermediate for a new drug candidate. By incorporating 3-Carboxy-2-Fluorophenylboronic Acid into their reaction conditions, they successfully achieved the desired chemo selectivity, leading to a higher yield and purity of the intermediate.

Case Study 2: Synthesis of Biologically Active Compounds

Company B, a biotech company specializing in the development of natural products, utilized 3-Carboxy-2-Fluorophenylboronic Acid in the synthesis of a novel biologically active compound. The compound exhibited promising activity against a specific target, and the use of this synthesis aid played a crucial role in achieving the desired selectivity.

Soluções

3-Carboxy-2-Fluorophenylboronic Acid offers several solutions for chemo selectivity challenges:

  • Improves the selectivity of Suzuki coupling reactions
  • Facilitates the synthesis of biologically active compounds
  • Enhances the yield and purity of pharmaceutical intermediates

Orientação especializada

When using 3-Carboxy-2-Fluorophenylboronic Acid, it is essential to follow expert guidance to ensure optimal results. Here are some key points to consider:

  • Otimizar as condições de reação, tais como a temperatura, a pressão e a escolha do solvente
  • Monitor reaction progress using appropriate analytical techniques
  • Perform purification steps to achieve high purity of the desired product

Conclusão

In conclusion, 3-Carboxy-2-Fluorophenylboronic Acid is a valuable synthesis aid for addressing chemo selectivity challenges in chemical reactions. Its applications in various fields, such as pharmaceuticals and biotechnology, highlight its importance in achieving high yields and purities of desired products. By following expert guidance and optimizing reaction conditions, users can effectively utilize this compound to overcome chemo selectivity issues.

Palavras-chave

3-Carboxy-2-Fluorophenylboronic Acid, chemo selectivity, synthesis aid, Suzuki coupling, pharmaceutical intermediates, biologically active compounds

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