Phenols
Items 61 to 64 of 64 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
HBED | 35369-53-0 | sc-200817 sc-200817A sc-200817B | 50 mg 250 mg 1 g | $72.00 $225.00 $367.00 | 2 | |
HBED is a phenolic compound characterized by its ability to form stable chelates with metal ions, enhancing its role in coordination chemistry. The presence of multiple hydroxyl groups facilitates strong hydrogen bonding, which can significantly alter its solubility and reactivity. Its unique electronic structure allows for effective π-π stacking interactions, influencing its behavior in various chemical environments and contributing to its kinetic properties in complexation reactions. | ||||||
Myricetin | 529-44-2 | sc-203147 sc-203147A sc-203147B sc-203147C sc-203147D | 25 mg 100 mg 1 g 25 g 100 g | $95.00 $184.00 $255.00 $500.00 $1002.00 | 3 | |
Myricetin is a flavonoid phenol known for its intricate molecular structure, which features multiple hydroxyl groups that enhance its antioxidant capacity. This compound exhibits notable redox properties, allowing it to engage in electron transfer reactions. Its ability to form hydrogen bonds and engage in π-π interactions contributes to its stability in various solvents, influencing its reactivity and interaction with other biomolecules. Myricetin's unique configuration also allows for selective binding to certain proteins, impacting its behavior in biochemical pathways. | ||||||
3-Hydroxyanthranilic acid | 548-93-6 | sc-216460 sc-216460A sc-216460B sc-216460C sc-216460D | 250 mg 1 g 5 g 10 g 25 g | $66.00 $143.00 $194.00 $344.00 $717.00 | 1 | |
3-Hydroxyanthranilic acid is a phenolic compound characterized by its unique ability to participate in complex hydrogen bonding networks, which significantly influences its solubility and reactivity. This compound can undergo tautomerization, leading to distinct isomeric forms that exhibit varied reactivity profiles. Its aromatic structure allows for effective π-π stacking interactions, enhancing its stability in diverse environments. Additionally, it plays a role in metabolic pathways, showcasing its involvement in various biochemical processes. | ||||||
Combrestatin A4 | 117048-59-6 | sc-204697 sc-204697A | 1 mg 5 mg | $45.00 $79.00 | ||
Combrestatin A4 is a phenolic compound notable for its intricate molecular interactions, particularly its capacity for π-π stacking and hydrophobic interactions, which enhance its stability in solution. This compound exhibits unique reactivity through electrophilic aromatic substitution, allowing it to form diverse derivatives. Its rigid structure facilitates specific conformational arrangements, influencing its behavior in various chemical environments and contributing to its distinct kinetic properties. | ||||||