Efficient Synthesis Aid： IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE for Challenging Organic Reactions

Efficient Synthesis Aid: IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE for Challenging Organic Reactions

Efficient Synthesis Aid: IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE is a cutting-edge organic synthesis reagent designed to facilitate challenging organic reactions. This guide provides a comprehensive overview of the product, including its parameters, usage scenarios, case studies, solutions, and expert guidance.

Product Overview

IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE is a versatile reagent that can be used in various organic synthesis reactions. It is a white crystalline solid with a melting point of 123-125°C. The molecular formula is C₈H₅N₃, and the molecular weight is 155.14 g/mol. The product is highly pure, with a purity of ≥98%. It is stable under normal storage conditions and should be stored in a cool, dry place away from direct sunlight.

Usage Scenarios

IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE is particularly useful in the synthesis of complex organic molecules, including heterocyclic compounds, pharmaceutical intermediates, and fine chemicals. It can be used in various reaction types, such as:

These reactions are often challenging due to the presence of sensitive functional groups or the need for high selectivity. IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE can help overcome these challenges and improve the efficiency of the synthesis process.

Case Studies

Here are two case studies demonstrating the effectiveness of IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE in challenging organic reactions:

Case Study 1: Synthesis of a Heterocyclic Compound

Company A was struggling to synthesize a complex heterocyclic compound with a specific structure. The synthesis involved a condensation reaction, which was difficult due to the presence of sensitive functional groups. By using IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE, Company A was able to achieve high yields and excellent purity of the desired compound. The reaction conditions were optimized, and the overall process was simplified, resulting in significant cost savings.

Case Study 2: Synthesis of a Pharmaceutical Intermediate

Company B was working on the development of a new pharmaceutical intermediate. The synthesis required a reduction reaction, which was challenging due to the presence of a nitro group. By using IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE, Company B was able to achieve high yields and excellent purity of the intermediate. The reaction conditions were optimized, and the overall process was simplified, resulting in a shorter development timeline and reduced costs.

Solutions

IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE offers several advantages for challenging organic reactions:

• High purity and stability
• Excellent reactivity and selectivity
• Easy to handle and use
• Cost-effective

These advantages make IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE an ideal choice for researchers and industrial chemists working on complex organic synthesis.

Expert Guidance

For optimal results, it is recommended to follow the guidelines provided by the manufacturer. These guidelines include:

• Storing the product in a cool, dry place away from direct sunlight
• Handling the product with appropriate safety equipment, such as gloves and goggles
• Optimizing reaction conditions, such as temperature, pressure, and solvent choice

By following these guidelines, users can maximize the efficiency and success of their organic synthesis reactions.

Summary

IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE is a powerful and versatile reagent for challenging organic reactions. Its high purity, stability, and reactivity make it an ideal choice for researchers and industrial chemists. By following the guidelines provided by the manufacturer and optimizing reaction conditions, users can achieve high yields and excellent purity of their desired compounds.

Keywords

IMIDAZO[1,2-A]PYRIDINE-6-CARBONITRILE, organic synthesis, heterocyclic compounds, pharmaceutical intermediates, fine chemicals, condensation, reduction, hydroamination

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