(R)-(+)-1-(1-Naphthyl)ethylamine Cinacalcet Impurity A

Unlock the versatile potential of (R)-(+)-1-(1-Naphthyl)ethylamine, a captivating chemical compound that serves as Cinacalcet Impurity A. This remarkable molecule, identified by the CAS number 3886-70-2, is a valuable asset in the realm of organic synthesis and chiral chemistry. With its unique structural features and exceptional purity, this compound opens up a world of possibilities for researchers and scientists seeking to push the boundaries of their work.

At the heart of this compound lies a captivating naphthyl moiety, which is paired with a chiral ethylamine group. This distinctive combination endows (R)-(+)-1-(1-Naphthyl)ethylamine with a remarkable ability to participate in a diverse array of organic reactions, making it a coveted tool in the hands of skilled chemists. Whether you're exploring the synthesis of β-amino acids or delving into the enantioselective reduction of ketones to nitroolefins, this versatile compound can be your key to unlocking groundbreaking discoveries.

Chiral Synthesis and Organic Reactions

The true power of (R)-(+)-1-(1-Naphthyl)ethylamine lies in its exceptional chiral properties. As an enantiomerically pure compound, it can serve as a valuable chiral auxiliary or catalyst, enabling the precise control and manipulation of stereochemistry in organic transformations. This precision is crucial in the synthesis of complex molecules, where the correct spatial arrangement of atoms can mean the difference between success and failure.

Researchers have long recognized the versatility of this compound, leveraging its unique characteristics in a wide range of applications. From the synthesis of β-amino acids to the enantioselective reduction of ketones to nitroolefins, (R)-(+)-1-(1-Naphthyl)ethylamine has proven to be an indispensable tool in the chemist's arsenal. Its ability to selectively participate in these reactions, while maintaining high levels of purity and consistency, makes it a sought-after reagent in the world of organic synthesis.

Technical Specifications and Handling

Meticulously crafted to meet the highest standards of quality, (R)-(+)-1-(1-Naphthyl)ethylamine boasts an impressive set of technical specifications. With a chemical formula of C₁₂H₁₃N, a molecular weight of 171.24 g/mol, and a distinct pale yellow to yellow oil appearance, this compound is a testament to the precision of modern chemistry.

To ensure the longevity and stability of this valuable reagent, it is recommended to store (R)-(+)-1-(1-Naphthyl)ethylamine at a temperature of +4°C. This controlled environment helps maintain the compound's purity and integrity, allowing researchers to rely on consistent and reliable results in their experiments.

When handling this compound, it is essential to follow standard laboratory safety protocols. While the specific hazard information is yet to be confirmed, it is always prudent to exercise caution, wear appropriate personal protective equipment, and work in a well-ventilated area. By adhering to these guidelines, you can ensure the safe and effective use of (R)-(+)-1-(1-Naphthyl)ethylamine in your research endeavors.

Unlock the Potential

As you embark on your next project, consider the transformative power of (R)-(+)-1-(1-Naphthyl)ethylamine. This captivating compound, with its unique structural features and exceptional chiral properties, is poised to become your indispensable partner in the pursuit of groundbreaking discoveries. Whether you're exploring the realms of pharmaceutical development, agrochemical innovation, or advanced material science, this versatile reagent can help you unlock new possibilities and push the boundaries of what's achievable.

Immerse yourself in the wealth of information available on this remarkable compound, from technical data sheets to peer-reviewed literature. Harness the expertise