Ketones
Items 211 to 214 of 214 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
9-Heptadecanone | 540-08-9 | sc-278657 | 5 g | $111.00 | ||
9-Heptadecanone, a long-chain ketone, exhibits unique properties stemming from its hydrophobic nature and extended carbon backbone. This structure promotes significant van der Waals interactions, influencing its phase behavior and solubility in nonpolar solvents. The carbonyl group is prone to nucleophilic attack, facilitating diverse reaction pathways. Additionally, its molecular conformation allows for potential conformational isomerism, affecting its reactivity and interactions in complex mixtures. | ||||||
1,3-Acetonedicarboxylic acid | 542-05-2 | sc-255915 sc-255915A sc-255915B | 50 g 250 g 1 kg | $53.00 $220.00 $800.00 | ||
1,3-Acetonedicarboxylic acid, a dicarboxylic acid with ketone functionality, showcases intriguing reactivity due to its dual acidic and carbonyl groups. This compound can engage in intramolecular hydrogen bonding, enhancing its stability and influencing its solubility in polar solvents. The presence of two carboxyl groups allows for unique dimerization and esterification reactions, while its ketone moiety can participate in condensation reactions, expanding its synthetic versatility. | ||||||
Paeonol | 552-41-0 | sc-205787 sc-205787A | 1 g 5 g | $33.00 $160.00 | 1 | |
Paeonol, a naturally occurring compound with ketone characteristics, exhibits notable reactivity through its aromatic structure and hydroxyl group. This configuration allows for strong π-π stacking interactions, enhancing its stability in various environments. The ketone functionality facilitates nucleophilic addition reactions, while the presence of the hydroxyl group can engage in hydrogen bonding, influencing solubility and reactivity in polar media. Its unique electronic properties also enable selective oxidation pathways. | ||||||
Chalcone | 614-47-1 | sc-204681 sc-204681A | 25 g 100 g | $49.00 $88.00 | 6 | |
Chalcone, a versatile compound classified as a ketone, features a conjugated double bond system that enhances its electrophilic character. This structure promotes significant resonance stabilization, allowing for efficient participation in Michael addition reactions. The compound's planar geometry facilitates strong intermolecular interactions, such as π-π stacking and dipole-dipole interactions, which can influence its solubility and reactivity in various solvents. Additionally, its unique electronic configuration enables selective photochemical transformations. | ||||||