1-Phenyl-5-mercapto CAS:86-93-1
Catalog Number | XD96253 |
Product Name | 1-Phenyl-5-mercapto |
CAS | 86-93-1 |
Molecular Formula | C7H6N4S |
Molecular Weight | 178.21 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
1-Phenyl-5-mercapto is a chemical compound that contains a phenyl group (C6H5) and a mercapto group (SH) attached to a central carbon atom. This particular arrangement of functional groups imparts specific chemical and physical effects to the compound, allowing it to be used in various applications.One effect of 1-phenyl-5-mercapto is its influence on the reactivity of the compound. The phenyl group is a hydrophobic aromatic moiety that can participate in various chemical reactions. It can undergo electrophilic aromatic substitution, allowing for the introduction of different substituents onto the phenyl ring. The mercapto group, on the other hand, is a nucleophilic group that can react with electrophiles, such as carbonyl compounds or halogens, to form covalent bonds. This combination of both electrophilic and nucleophilic reactivity makes 1-phenyl-5-mercapto a versatile compound in organic synthesis.Another effect of 1-phenyl-5-mercapto is its impact on the compound's physical properties. The phenyl group can influence the compound's solubility and melting point due to its nonpolar nature. The presence of the mercapto group can also influence the compound's stability, especially under oxidative conditions, due to the ability of the sulfur atom to undergo oxidation. These physical properties are crucial in determining the compound's suitability for various applications, including as a starting material in the synthesis of pharmaceuticals or as an additive in material science.In addition to its reactivity and physical properties, 1-phenyl-5-mercapto can also exhibit biological effects. The presence of the phenyl group can influence the compound's lipophilicity, which can enhance its permeability through cellular membranes. This property is often desirable in drug design to improve the compound's bioavailability. Furthermore, the mercapto group has the potential to exhibit antioxidant properties due to the ability of the sulfur atom to scavenge reactive oxygen species. This antioxidant effect can be beneficial in the treatment of oxidative stress-related diseases.Overall, 1-phenyl-5-mercapto possesses diverse effects on the compound's reactivity, physical properties, and potentially its biological activity. The combination of the phenyl and mercapto groups provides versatility and potential applications in organic synthesis, material science, and pharmaceutical development. The compound's reactivity allows for various chemical transformations, its physical properties can be tuned to suit specific needs, and its potential biological effects suggest it could have therapeutic applications. Therefore, 1-phenyl-5-mercapto is a valuable compound with potential uses in both research and industrial settings.