Carbonyl Compounds
Items 231 to 236 of 236 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2,3,4,5,6-Pentafluorocinnamic acid | 719-60-8 | sc-280296 | 10 g | $459.00 | ||
2,3,4,5,6-Pentafluorocinnamic acid is a distinctive carbonyl compound featuring a highly electronegative fluorinated structure that significantly alters its reactivity profile. The presence of multiple fluorine atoms enhances its acidity and stabilizes resonance structures, promoting unique electrophilic interactions. This compound exhibits rapid reaction kinetics in condensation and addition reactions, making it a versatile intermediate in organic synthesis. Its strong dipole moment influences solubility and intermolecular interactions, further affecting its behavior in various chemical environments. | ||||||
Farnesylacetone | 762-29-8 | sc-235124 | 50 g | $110.00 | ||
Farnesylacetone is a notable carbonyl compound characterized by its unique structural features, including a long hydrocarbon chain that influences its reactivity. The compound exhibits distinct steric effects, which can modulate reaction pathways and selectivity in nucleophilic attacks. Its carbonyl group participates in hydrogen bonding, enhancing solubility in polar solvents. Additionally, Farnesylacetone's molecular conformation can lead to varied kinetic profiles in reactions, making it an intriguing subject for studies in organic chemistry. | ||||||
2′-Aminoacetophenone | 551-93-9 | sc-231237 | 5 g | $27.00 | ||
2'-Aminoacetophenone, a notable carbonyl compound, exhibits intriguing reactivity due to its amino and carbonyl functional groups, which can engage in hydrogen bonding and nucleophilic attacks. This dual functionality allows for diverse synthetic pathways, including acylation and condensation reactions. Its polar nature enhances solubility in various solvents, while the presence of the aromatic ring contributes to its stability and potential for π-π interactions, influencing its behavior in complex chemical environments. | ||||||
Biphenyl-4,4′-dicarboxylic acid | 787-70-2 | sc-239346 sc-239346A | 5 g 25 g | $117.00 $405.00 | ||
Biphenyl-4,4'-dicarboxylic acid is a notable carbonyl compound characterized by its two carboxylic acid groups attached to a biphenyl structure. This arrangement facilitates strong intermolecular hydrogen bonding, enhancing its solubility in polar solvents. The compound exhibits unique reactivity patterns, particularly in esterification and amidation reactions, where its dual carboxyl groups can participate in diverse coupling mechanisms. Its rigid biphenyl framework also influences steric effects, impacting reaction kinetics and selectivity in synthetic applications. | ||||||
N-Allylurea | 557-11-9 | sc-235990 | 25 g | $41.00 | ||
N-Allylurea, a notable carbonyl compound, exhibits intriguing reactivity due to its dual functional groups. The presence of the allyl moiety allows for unique electrophilic interactions, enabling selective addition reactions with nucleophiles. Its carbonyl group participates in hydrogen bonding, enhancing solubility in polar solvents. This compound also demonstrates distinct thermal stability, influencing its behavior in polymerization processes and facilitating the formation of diverse adducts through Michael addition pathways. | ||||||
Methyl 3-pentenoate | 818-58-6 | sc-235738 | 5 ml | $115.00 | ||
Methyl 3-pentenoate is a distinctive carbonyl compound featuring a conjugated double bond adjacent to an ester functional group. This configuration allows for unique electronic interactions, enhancing its reactivity in Michael addition and Diels-Alder reactions. The compound's unsaturation contributes to its ability to undergo polymerization, while its ester moiety can engage in transesterification processes. Additionally, the spatial arrangement of its substituents influences its stereochemical properties, affecting reaction pathways and selectivity in synthetic transformations. | ||||||