Efficient 4-BENZYLAMINO-3-NITROPYRIDINE Solutions for Chemical Synthesis Challenges
Abstract
This article provides a comprehensive guide on the efficient use of 4-Benzylamino-3-nitropyridine in chemical synthesis challenges. It delves into the product parameters, usage scenarios, case studies, solutions, and expert guidance, aiming to assist users in overcoming chemical synthesis hurdles effectively.
1. Product Parameters
4-Benzylamino-3-nitropyridine, also known as BANP, is a versatile organic compound with a molecular formula of C10H7N3O. It is a white crystalline solid with a melting point of 123-125°C. The compound is highly reactive and can be used as a building block in various chemical syntheses. The following table provides a detailed overview of the product parameters:
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Parameter | Value |
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Molecular Formula | C10H7N3O |
Molecular Weight | 191.19 g/mol |
Appearance | White crystalline solid |
Melting Point | 123-125°C |
Solubility | Soluble in organic solvents such as chloroform, acetone, and ethanol |
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2. Usage Scenarios
4-Benzylamino-3-nitropyridine finds extensive applications in various chemical synthesis scenarios. Some of the common usage scenarios include:
- Synthesis of heterocyclic compounds
- Synthesis of pharmaceutical intermediates
- Synthesis of agrochemicals
- Synthesis of organic dyes and pigments
The versatility of BANP makes it a valuable compound in the chemical industry.
3. Case Studies
Here are a few case studies showcasing the use of 4-Benzylamino-3-nitropyridine in chemical synthesis:
- Case Study 1: Synthesis of a pharmaceutical intermediate
A pharmaceutical company used 4-Benzylamino-3-nitropyridine to synthesize a key intermediate for a new drug. The intermediate was successfully obtained with high purity and yield, enabling the company to proceed with the drug development process.
- Case Study 2: Synthesis of a heterocyclic compound
A research group synthesized a novel heterocyclic compound using 4-Benzylamino-3-nitropyridine as a key building block. The compound exhibited interesting biological properties, opening up new avenues for drug discovery.
- Case Study 3: Synthesis of an agrochemical
An agrochemical company utilized 4-Benzylamino-3-nitropyridine to synthesize a new agrochemical with improved efficacy. The compound was successfully synthesized with high purity and yield, contributing to the company's product portfolio.
4. Solutions
To overcome chemical synthesis challenges, it is essential to use 4-Benzylamino-3-nitropyridine efficiently. Here are some solutions to consider:
- Optimize reaction conditions: Adjusting reaction temperature, pressure, and solvent can enhance the yield and purity of the desired product.
- Use appropriate catalysts: Catalysts can significantly improve the efficiency of chemical reactions, reducing reaction time and energy consumption.
- Employ green chemistry principles: Utilize environmentally friendly solvents, reagents, and reaction conditions to minimize the environmental impact of chemical synthesis.
5. Expert Guidance
Consulting with experts in the field of chemical synthesis can provide valuable insights and guidance. Here are some tips from experts:
- Choose the right starting material: Selecting the appropriate starting material can significantly impact the efficiency of the synthesis process.
- Optimize reaction conditions: Experiment with different reaction conditions to find the optimal conditions for your specific synthesis.
- Stay updated with the latest research: Keep abreast of the latest advancements in chemical synthesis techniques and methodologies.
6. Conclusion
In conclusion, 4-Benzylamino-3-nitropyridine is a valuable compound in chemical synthesis, offering numerous advantages in terms of versatility, reactivity, and efficiency. By understanding its product parameters, usage scenarios, case studies, solutions, and expert guidance, users can effectively overcome chemical synthesis challenges and achieve successful outcomes.
Keywords
4-Benzylamino-3-nitropyridine, chemical synthesis, pharmaceutical intermediates, agrochemicals, heterocyclic compounds, green chemistry
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