Melhore a sua investigação com soluções de metanossulfonato de (2S)-2-[(1,1-Dimetiletil)oxi]carbonilaminopropilo CAS 109687-66-3

2025-3-21

Resumo

This article provides a comprehensive guide on enhancing research with (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3 solutions. It covers product parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs to help researchers make informed decisions.

Visão geral do produto

(2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3 is a versatile research chemical used in various applications. This guide aims to provide a detailed understanding of the product, its usage, and its benefits in research.

Parâmetros do produto

Table 1: Product Parameters of (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3

Parâmetro	Valor
Fórmula química	C₁₀H₁₉N₂O₄S
Peso molecular	244.34 g/mol
Aparência	Pó cristalino branco a esbranquiçado
Pureza	≥98%

Cenários de utilização

(2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3 is widely used in various research fields, including:

Biological research: Studying protein-protein interactions, enzyme inhibition, and drug discovery.
Chemical synthesis: Synthesizing novel organic compounds and exploring new reaction pathways.
Material science: Developing new materials with improved properties.

Estudos de caso

Case Study 1: Dr. Smith, a researcher at XYZ University, used (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3 to study protein-protein interactions. The compound helped in identifying novel protein interactions, leading to the development of potential therapeutic targets.

Case Study 2: Dr. Johnson, a chemist at ABC Research Institute, utilized the compound for synthesizing a novel organic compound. The synthesis process was successful, and the resulting compound exhibited promising properties for potential applications in pharmaceuticals.

Soluções

1. Optimizing reaction conditions: Researchers can optimize reaction conditions, such as temperature, pressure, and solvent choice, to enhance the yield and purity of the desired product.

2. Purification techniques: Utilizing advanced purification techniques, such as recrystallization, chromatography, and crystallization, can help in obtaining high-purity (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3.

3. Scale-up: Scaling up the synthesis process from laboratory to industrial scale requires careful optimization of reaction parameters and equipment to ensure consistent product quality.

Orientação especializada

Consulting with experts in the field can provide valuable insights into the usage and optimization of (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3. Experts can offer guidance on reaction conditions, purification techniques, and scale-up processes.

FAQs

Q: What is the storage condition for (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3?

A: Store the compound in a cool, dry place, away from direct sunlight and moisture. Keep it in a tightly sealed container.

Q: How can I ensure the purity of the compound?

A: Use advanced purification techniques, such as recrystallization, chromatography, and crystallization, to obtain high-purity (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3.

Conclusão

In conclusion, (2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate CAS 109687-66-3 is a valuable research chemical with wide applications in various fields. By understanding its product parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs, researchers can make informed decisions and enhance their research outcomes.

Palavras-chave

(2S)-2-[(1,1-Dimethylethyl)oxy]carbonylaminopropyl Methanesulfonate, CAS 109687-66-3, research chemical, biological research, chemical synthesis, material science, protein-protein interactions, enzyme inhibition, drug discovery.