CAS 1334513-02-8 Decoded: The Key to Understanding N-[(S)-(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-L-Alanine 1-Methylethyl Ester

Abstract

This article delves into the chemical compound CAS 1334513-02-8, specifically N-[(S)-(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-L-Alanine 1-Methylethyl Ester. The compound is discussed from various angles, including its chemical structure, synthesis, biological significance, potential applications, and safety considerations. The aim is to provide a comprehensive understanding of this compound, highlighting its unique properties and its role in modern chemistry and pharmaceutical research.

Introduction to CAS 1334513-02-8

CAS 1334513-02-8, also known as N-[(S)-(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-L-Alanine 1-Methylethyl Ester, is a complex organic compound with a unique chemical structure. It belongs to the class of phosphorus-containing organic compounds and is characterized by the presence of a pentafluorophenoxy group and a phosphinyl group. This compound has garnered attention in the fields of chemistry and pharmaceutical research due to its potential applications and unique properties.

Chemical Structure and Composition

The chemical structure of CAS 1334513-02-8 is quite intricate. It consists of a phosphorus atom bonded to a phenyl group, which in turn is attached to a pentafluorophenoxy group. This phosphinyl group is further linked to an alanine molecule, which is esterified with a 1-methylethyl group. The presence of the pentafluorophenoxy group imparts unique electronic properties to the compound, making it a subject of interest in various chemical reactions.

Synthesis and Preparation

The synthesis of CAS 1334513-02-8 involves a series of chemical reactions that lead to the formation of the desired compound. The process typically starts with the preparation of the pentafluorophenoxyphosphine, which is then reacted with L-alanine to form the phosphinylalanine derivative. Subsequently, the esterification reaction with 1-methylethanol yields the final compound. The synthesis process requires careful control of reaction conditions to ensure the desired product is obtained.

Biological Significance

The biological significance of CAS 1334513-02-8 is still under investigation, but it is believed to have potential applications in the pharmaceutical industry. The unique structure of the compound suggests that it may interact with biological molecules in specific ways, potentially leading to novel therapeutic agents. Further research is needed to explore its potential in drug discovery and development.

Potential Applications

The potential applications of CAS 1334513-02-8 are diverse. Its unique chemical properties make it a candidate for various synthetic reactions, including cross-coupling reactions and Suzuki coupling. In the pharmaceutical sector, the compound could serve as a building block for the synthesis of new drugs or as a lead compound for further optimization. Additionally, its potential in material science cannot be overlooked, as the compound’s properties may be harnessed for the development of novel materials.

Safety Considerations

As with any chemical compound, safety considerations are paramount when dealing with CAS 1334513-02-8. The compound is known to be toxic and should be handled with appropriate care. It is essential to use personal protective equipment, such as gloves and lab coats, when working with this substance. Proper ventilation and adherence to standard laboratory safety protocols are also crucial to prevent any potential hazards.

Conclusion

CAS 1334513-02-8, N-[(S)-(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-L-Alanine 1-Methylethyl Ester, is a complex organic compound with a range of potential applications. Its unique chemical structure and properties make it a subject of interest in various scientific disciplines. While further research is needed to fully understand its biological significance and potential applications, the compound holds promise for future advancements in chemistry and pharmaceutical research.

Keywords

CAS 1334513-02-8, N-[(S)-(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-L-Alanine 1-Methylethyl Ester, chemical structure, synthesis, biological significance, potential applications, safety considerations

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