Quinolines
Items 131 to 135 of 135 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
1,2,3,4-Tetrahydro-benzo[h]quinolin-3-ol | 5423-67-6 | sc-273542 | 250 mg | $92.00 | ||
1,2,3,4-Tetrahydro-benzo[h]quinolin-3-ol is a notable quinoline derivative characterized by its unique hydrogen bonding capabilities and structural rigidity. The presence of hydroxyl groups enhances its ability to engage in intramolecular interactions, influencing its reactivity and stability. This compound exhibits distinct photophysical properties, allowing for effective light absorption and emission, which can impact its behavior in photochemical reactions and electron transfer mechanisms. | ||||||
Coptisin chloride | 6020-18-4 | sc-281638 | 10 mg | $459.00 | ||
Coptisin chloride, a member of the quinoline family, showcases intriguing electronic properties due to its conjugated system, which facilitates efficient charge transfer. Its unique chlorine substituent enhances electrophilic reactivity, allowing for selective interactions with nucleophiles. The compound's planar structure promotes stacking interactions, influencing its solubility and aggregation behavior in various environments. Additionally, its distinct fluorescence characteristics can be leveraged in studies of molecular dynamics and environmental sensing. | ||||||
O-Methylviridicatin | 6152-57-4 | sc-202255 | 1 mg | $178.00 | 1 | |
O-Methylviridicatin, classified within the quinoline group, exhibits remarkable photophysical properties attributed to its extended π-conjugation, which enhances light absorption and emission. The presence of a methoxy group modifies its electronic distribution, influencing reactivity and interaction with metal ions. Its rigid, planar conformation facilitates π-π stacking, impacting its solubility and aggregation in different solvents. This compound also demonstrates unique redox behavior, making it a subject of interest in electron transfer studies. | ||||||
Quinidine sulfate dihydrate | 6591-63-5 | sc-205967 | 5 g | $67.00 | ||
Quinidine sulfate dihydrate, a member of the quinoline family, showcases intriguing electrochemical properties due to its nitrogen-containing heterocycle, which enhances its ability to participate in electron transfer processes. Its dual chiral centers contribute to distinct stereochemical interactions, influencing its solubility and reactivity in various environments. The compound's ability to form hydrogen bonds and engage in π-π interactions further affects its stability and behavior in complexation reactions. | ||||||
Hydroxychloroquine Sulfate | 747-36-4 | sc-215157 sc-215157A | 10 mg 100 mg | $26.00 $122.00 | 2 | |
Hydroxychloroquine Sulfate is an antimalarial and antirheumatic | ||||||