This article provides a comprehensive guide to the compound Sodium 2-Phenylindole-5-Sulfonate, CAS 119205-39-9. It delves into its chemical properties, applications, synthesis methods, safety considerations, and its significance in various scientific fields. By exploring these aspects, the article aims to offer a thorough understanding of this compound, making it a must-read for researchers, scientists, and anyone interested in the field of organic chemistry.
Sodium 2-Phenylindole-5-Sulfonate, with the CAS number 119205-39-9, is a synthetic organic compound that belongs to the indole sulfonate family. It is widely recognized for its unique chemical properties and diverse applications in research and industry. This guide aims to explore the power of this compound, highlighting its significance and potential uses.
Sodium 2-Phenylindole-5-Sulfonate is a white to off-white crystalline solid that is soluble in water and organic solvents. It possesses a molecular formula of C13H10N2NaO4S and a molecular weight of 274.27 g/mol. The compound contains a phenyl group, an indole ring, and a sulfonic acid group, which contribute to its chemical reactivity and versatility. These properties make it a valuable tool in various chemical reactions and applications.
Sodium 2-Phenylindole-5-Sulfonate has found extensive applications in scientific research. Its unique chemical properties make it suitable for use in various experiments, including enzyme assays, protein purification, and drug discovery. For instance, it can be used as a substrate for enzymes, allowing researchers to study their activity and specificity. Additionally, its ability to bind to proteins makes it a valuable tool in protein purification processes.
The synthesis of Sodium 2-Phenylindole-5-Sulfonate involves several steps, including the preparation of the indole ring and the sulfonation process. The indole ring can be synthesized through various methods, such as the Knoevenagel condensation or the Biginelli reaction. Once the indole ring is obtained, it is subjected to sulfonation using sulfuric acid or other sulfonating agents. The resulting compound is then purified through recrystallization or other purification techniques.
As with any chemical compound, safety considerations are crucial when handling Sodium 2-Phenylindole-5-Sulfonate. It is important to wear appropriate personal protective equipment, such as gloves, goggles, and lab coats, when working with this compound. Adequate ventilation is also essential to prevent inhalation of dust or fumes. Furthermore, proper disposal methods should be followed to minimize environmental impact.
Sodium 2-Phenylindole-5-Sulfonate plays a significant role in various scientific fields. In the pharmaceutical industry, it is used as a starting material for the synthesis of new drugs and pharmaceutical intermediates. In the field of biochemistry, it is employed in the study of enzyme kinetics and protein purification. Additionally, its applications extend to materials science, where it can be used in the development of new materials with unique properties.
In conclusion, Sodium 2-Phenylindole-5-Sulfonate, CAS 119205-39-9, is a versatile and valuable compound with diverse applications in scientific research and industry. Its unique chemical properties, coupled with its significance in various scientific fields, make it a must-read for anyone interested in the field of organic chemistry. By understanding its synthesis, safety considerations, and applications, researchers and scientists can harness the power of this compound to advance their work and contribute to the development of new technologies and materials.
Keywords: Sodium 2-Phenylindole-5-Sulfonate, CAS 119205-39-9, organic chemistry, synthesis, applications, safety considerations