| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Naphthol AS-MX phosphate disodium salt | 96189-12-7 | sc-215539 sc-215539A sc-215539B | 100 mg 500 mg 1 g | $58.00 $133.00 $222.00 | 1 | |
Naphthol AS-MX phosphate disodium salt exhibits unique properties as an acid catalyst, facilitating electrophilic aromatic substitution reactions. Its structure allows for strong hydrogen bonding interactions, enhancing reactivity and selectivity in various chemical pathways. The compound's amphiphilic characteristics promote solubility in both polar and nonpolar solvents, enabling versatile applications in complex reaction environments. Additionally, its ability to stabilize transition states contributes to improved reaction kinetics, making it a valuable component in synthetic processes. | ||||||
Naphthol AS-BI-phosphate disodium salt | 530-79-0 | sc-219334 sc-219334A | 100 mg 500 mg | $66.00 $112.00 | ||
Naphthol AS-BI-phosphate, disodium salt, serves as an effective acid catalyst, promoting nucleophilic attack in aromatic systems. Its unique molecular architecture fosters specific π-π stacking interactions, enhancing the stability of intermediates. The compound's dual solubility profile allows it to engage in diverse reaction media, while its capacity to modulate electronic environments aids in fine-tuning reaction pathways. This versatility supports efficient catalysis in complex organic transformations. | ||||||
Naphthol AS-BI-phosphate | 1919-91-1 | sc-222042 sc-222042A | 100 mg 1 g | $98.00 $288.00 | 1 | |
Naphthol AS-BI-phosphate exhibits remarkable properties as an acid catalyst, facilitating electrophilic aromatic substitution reactions. Its unique structure enables strong hydrogen bonding interactions, which stabilize transition states and enhance reaction rates. The compound's amphiphilic nature allows it to interact with both polar and nonpolar substrates, promoting diverse reaction conditions. Additionally, its ability to influence charge distribution within aromatic systems contributes to selective reactivity, making it a valuable tool in synthetic chemistry. | ||||||