Items 191 to 200 of 233 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Davercin | 55224-05-0 | sc-391506 | 1 mg | $150.00 | ||
Davercin is a rare and high-purity acid halide known for its distinctive reactivity profile. Its unique structural features promote selective electrophilic interactions, enabling efficient formation of acyl derivatives. The compound exhibits notable stability under specific conditions, which influences its reaction kinetics and pathways. Furthermore, its exceptional solubility in various solvents allows for versatile applications in complex synthetic routes, highlighting its potential in advanced chemical research. | ||||||
Alamethicin F50 | 56165-93-6 | sc-391715 | 2.5 mg | $260.00 | ||
Alamethicin F50 is a rare and high-purity compound characterized by its unique amphipathic structure, which facilitates specific interactions with lipid membranes. This property enhances its ability to form ion channels, influencing membrane permeability and ion transport dynamics. Its distinct conformational flexibility contributes to varied reaction pathways, while its high solubility in polar and non-polar solvents allows for diverse experimental setups, making it a subject of interest in advanced biochemical studies. | ||||||
Demethoxyviridiol | 56617-66-4 | sc-391780 | 1 mg | $250.00 | ||
Demethoxyviridiol is a rare and high-purity compound distinguished by its intricate stereochemistry, which enables selective binding to specific receptors and influences molecular recognition processes. Its unique functional groups facilitate diverse intermolecular interactions, enhancing its reactivity in various chemical environments. Additionally, its exceptional solubility profile allows for effective participation in complex reaction mechanisms, making it a compelling subject for in-depth chemical investigations. | ||||||
Actagardin | 59165-34-3 | sc-391713 | 1 mg | $315.00 | ||
Actagardin is a rare and high-purity acid halide characterized by its unique reactivity and selective electrophilic behavior. Its distinct carbonyl group enhances nucleophilic attack, leading to rapid acylation reactions. The compound exhibits remarkable stability under specific conditions, allowing for controlled transformations. Its ability to form stable intermediates and engage in diverse coupling reactions makes it an intriguing candidate for exploring novel synthetic pathways in organic chemistry. | ||||||
Enterocin | 59678-46-5 | sc-362021 | 1 mg | $200.00 | ||
Enterocin is a rare and high-purity acid halide known for its exceptional reactivity and specificity in chemical transformations. Its unique structure facilitates strong interactions with nucleophiles, promoting efficient acylation processes. The compound demonstrates remarkable selectivity in reaction kinetics, allowing for tailored synthesis. Additionally, Enterocin's ability to stabilize reactive intermediates opens avenues for innovative synthetic strategies, making it a compelling subject for advanced chemical research. | ||||||
Thiocillin I | 59979-01-0 | sc-391644 | 500 µg | $250.00 | ||
Thiocillin I is a rare and high-purity acid halide distinguished by its unique electrophilic character, which enhances its reactivity with a variety of nucleophiles. This compound exhibits a distinctive ability to form stable adducts, facilitating complex reaction pathways. Its high selectivity in acylation reactions allows for precise control over product formation, while its physical properties contribute to its role in innovative synthetic methodologies. Thiocillin I's behavior in diverse chemical environments makes it a fascinating subject for exploration in advanced chemistry. | ||||||
Quadrone | 66550-08-1 | sc-391537 | 500 µg | $315.00 | ||
Quadrone is a rare and high-purity acid halide characterized by its exceptional reactivity and specificity in nucleophilic acyl substitution reactions. Its unique steric and electronic properties enable it to engage in rapid reaction kinetics, often leading to the formation of highly stable intermediates. Quadrone's ability to participate in diverse molecular interactions allows for the development of intricate synthetic pathways, making it a compelling candidate for advanced chemical research. | ||||||
Maduramicin | 79356-08-4 | sc-362766 | 5 mg | $188.00 | ||
Maduramicin is a rare and high-purity acid halide distinguished by its selective reactivity and unique molecular architecture. Its distinctive functional groups facilitate specific interactions with nucleophiles, promoting efficient reaction pathways. The compound exhibits remarkable stability in various environments, allowing for controlled reaction kinetics. Additionally, its ability to form complex molecular assemblies enhances its potential for innovative applications in synthetic chemistry, driving forward research in advanced materials. | ||||||
Anhydroepiophiobolin A | 90411-20-4 | sc-391727 | 1 mg | $325.00 | ||
Anhydroepiophiobolin A is a rare and high-purity acid halide characterized by its intricate stereochemistry and unique reactivity profile. This compound engages in selective electrophilic interactions, enabling it to participate in diverse synthetic pathways. Its robust molecular framework contributes to enhanced stability under varying conditions, while its propensity to form transient intermediates allows for dynamic reaction kinetics. These features position it as a compelling subject for exploration in advanced chemical synthesis. | ||||||
Leucanicidin | 91021-66-8 | sc-391619 | 500 µg | $250.00 | ||
Leucanicidin is a rare and high-purity acid halide distinguished by its exceptional reactivity and specific molecular interactions. It exhibits a unique ability to form stable adducts through nucleophilic attack, facilitating intricate reaction pathways. The compound's distinctive electronic structure enhances its reactivity, allowing for rapid transformations. Additionally, its high purity ensures consistent performance in complex chemical environments, making it a fascinating candidate for in-depth research in synthetic chemistry. | ||||||