Aromatics
Items 21 to 30 of 367 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $153.00 | 5 | |
Ibrutinib is an irreversible Bruton′s tyrosine kinase inhibitor that selectively blocks B cell activation. | ||||||
CH 223191 | 301326-22-7 | sc-293991 sc-293991A | 10 mg 50 mg | $194.00 $831.00 | 2 | |
CH 223191 exhibits intriguing properties as an aromatic compound, characterized by its unique substituents that influence its reactivity and interaction with biological targets. The presence of specific halogen atoms alters the electron density, enhancing its ability to engage in π-π stacking interactions. This compound's structural features facilitate selective binding to certain receptors, impacting its kinetic behavior in various chemical environments. Its distinct molecular architecture contributes to unique pathways in reaction mechanisms, making it a subject of interest in studies of aromatic behavior. | ||||||
Flavopiridol Hydrochloride | 131740-09-5 | sc-207687 | 10 mg | $311.00 | ||
Flavopiridol Hydrochloride features a distinctive aromatic structure that promotes strong π-π stacking interactions, enhancing its stability in various environments. The presence of hydroxyl groups contributes to its ability to form hydrogen bonds, influencing solubility and reactivity. This compound exhibits notable selectivity in electrophilic aromatic substitution reactions, where its unique electronic distribution allows for controlled reactivity, making it a versatile participant in synthetic organic chemistry. | ||||||
n-Butylidenephthalide, (E)+(Z) | 551-08-6 | sc-279727 | 10 g | $87.00 | 1 | |
n-Butylidenephthalide, as an aromatic compound, showcases unique resonance stabilization through its conjugated double bonds, which enhances its reactivity in electrophilic aromatic substitution reactions. The compound's distinct geometric isomerism (E and Z forms) allows for varied interaction profiles with nucleophiles, influencing reaction pathways. Its hydrophobic character promotes selective solubility in non-polar solvents, affecting its behavior in diverse chemical environments and applications. | ||||||
BAPTA tetrapotassium salt | 73630-08-7 | sc-202076A sc-202076 | 100 mg 1 g | $112.00 $223.00 | 13 | |
BAPTA tetrapotassium salt is a chelating agent known for its ability to selectively bind calcium ions through its unique structure, which features multiple carboxylate groups. This compound exhibits distinct coordination chemistry, facilitating the formation of stable complexes that can modulate ion availability in various environments. Its high solubility in aqueous solutions enhances its reactivity, allowing for rapid interactions in biochemical pathways and influencing cellular signaling processes. | ||||||
AZD8055 | 1009298-09-2 | sc-364424 sc-364424A | 10 mg 50 mg | $160.00 $345.00 | 12 | |
AZD8055 is a synthetic aromatic compound notable for its intricate electronic structure, which facilitates strong intermolecular interactions, particularly through hydrogen bonding and π-stacking. This compound exhibits unique reactivity patterns, engaging in electrophilic aromatic substitution and demonstrating distinct kinetic profiles in various reaction environments. Its planar geometry enhances its stability and solubility in organic solvents, influencing its behavior in complex chemical systems. | ||||||
Dimethylnaphthalene, mixture of isomers | 28804-88-8 | sc-234759 | 50 g | $617.00 | ||
Dimethylnaphthalene, a complex mixture of isomers, exhibits unique molecular interactions due to its polycyclic aromatic structure. The presence of methyl groups enhances its hydrophobic character, influencing solubility and phase behavior in various environments. Its isomeric forms can engage in distinct reaction pathways, leading to varied kinetics in electrophilic aromatic substitutions. Additionally, the compound's ability to participate in π-π stacking interactions contributes to its stability and reactivity in complex chemical systems. | ||||||
Sodium tetraphenylborate | 143-66-8 | sc-212948 sc-212948A | 5 g 25 g | $30.00 $107.00 | ||
Sodium tetraphenylborate is a fascinating compound characterized by its unique boron-centered structure, which facilitates strong π-π interactions among its phenyl groups. This arrangement enhances its solubility in organic solvents and promotes distinct aggregation behaviors. The compound's ability to form stable complexes with various cations showcases its role in ion-selective processes, while its electron-rich nature allows for intriguing reactivity patterns in aromatic substitution reactions. | ||||||
PDM 2 | 688348-25-6 | sc-205428 sc-205428A | 10 mg 50 mg | $53.00 $315.00 | ||
PDM 2 is characterized by its unique aromatic framework, which is significantly influenced by its substituents that enhance electron delocalization. This compound exhibits distinct reactivity patterns due to its ability to engage in electrophilic aromatic substitution, driven by the electron-donating effects of its functional groups. Additionally, its molecular structure promotes specific stacking interactions, which can alter its physical properties and reactivity in various chemical environments. | ||||||
Acenaphthene | 83-32-9 | sc-254933 sc-254933A | 1 g 5 g | $29.00 $50.00 | ||
Acenaphthene is a polycyclic aromatic hydrocarbon characterized by its fused ring structure, which imparts unique electronic properties. Its planar geometry promotes strong π-π stacking interactions, enhancing its stability and solubility in organic solvents. The compound exhibits notable reactivity in electrophilic substitution reactions, where its electron-rich nature allows for rapid functionalization. Additionally, acenaphthene's distinct molecular interactions contribute to its behavior in various catalytic processes, making it a fascinating subject in materials science and organic synthesis. | ||||||