High-Purity 4-Carboxy-3-Nitrobenzylamine for Organic Synthesis
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4-Carboxy-3-Nitrobenzylamine
This fine chemical, identified by CAS 100466-28-2, is a crucial building block in the field of organic synthesis. Its high purity, meeting a standard of ≥98.0%, ensures reliable results in complex chemical reactions. As a versatile intermediate, it plays a vital role in creating advanced organic compounds for various applications.
- Discover the utility of 4-Carboxy-3-Nitrobenzylamine for organic synthesis, a critical component for researchers and manufacturers.
- Explore the benefits of sourcing high-purity 4-Carboxy-3-Nitrobenzylamine from trusted manufacturers to guarantee reaction success.
- Learn about the specifications of 4-Carboxy-3-Nitrobenzylamine CAS 100466-28-2, including its density and boiling point, for optimal handling and use.
- Investigate the applications of this essential chemical intermediate in developing novel materials and pharmaceuticals.
Key Advantages
Exceptional Purity
Benefit from the high-purity standard of ≥98.0% 4-Carboxy-3-Nitrobenzylamine, ensuring predictable outcomes in your organic synthesis projects.
Versatile Intermediate
Leverage the role of 4-Carboxy-3-Nitrobenzylamine CAS 100466-28-2 as a fundamental building block for a wide array of complex organic molecules.
Reliable Quality
Trust in the consistent quality and physical properties, such as a density of 1.466 g/cm³, of this chemical intermediate for dependable results.
Key Applications
Organic Synthesis
As a prime organic synthesis intermediate, this compound is essential for constructing intricate molecular structures used in pharmaceuticals and advanced materials.
Chemical Research
Researchers utilize 4-Carboxy-3-Nitrobenzylamine in laboratories for exploring new reaction pathways and developing innovative chemical entities.
Fine Chemical Production
Its role as a fine chemical makes it indispensable in the manufacturing processes of specialized chemical products.
Intermediate Synthesis
The compound serves as a critical intermediate in multi-step synthesis, facilitating the creation of more complex target molecules.