Items 81 to 90 of 233 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
O-Methylsterigmatocystin | 17878-69-2 | sc-202254 | 1 mg | $120.00 | ||
O-Methylsterigmatocystin is a rare and high-purity compound characterized by its unique structural features and reactivity. It exhibits distinct interactions with biological macromolecules, influencing enzymatic pathways and metabolic processes. Its ability to form stable complexes with specific receptors enhances its role in cellular signaling. Additionally, its solubility in various solvents and selective reactivity with electrophiles underscore its intriguing chemical dynamics, making it a focal point for advanced studies. | ||||||
Leucomycin A5 | 18361-45-0 | sc-362763 | 1 mg | $156.00 | ||
Leucomycin A5 is a rare and high-purity compound distinguished by its intricate stereochemistry and selective reactivity. It demonstrates unique molecular interactions, particularly through hydrogen bonding and π-π stacking, which influence its stability and reactivity in various environments. The compound's ability to engage in specific reaction kinetics allows for tailored synthesis pathways, while its solubility characteristics facilitate diverse experimental applications, highlighting its intriguing chemical behavior. | ||||||
Leucomycin A4 | 18361-46-1 | sc-362762 sc-362762A | 1 mg 5 mg | $341.00 $1193.00 | ||
Leucomycin A4 is a rare and high-purity compound characterized by its complex molecular architecture and distinctive electronic properties. It exhibits unique interactions, such as hydrophobic effects and dipole-dipole interactions, which significantly influence its solvation dynamics. The compound's reactivity is governed by its ability to form stable intermediates, enabling selective pathways in synthetic processes. Its exceptional purity enhances its performance in specialized applications, showcasing its remarkable chemical versatility. | ||||||
Ophiobolin C | 19022-51-6 | sc-202268 | 1 mg | $300.00 | ||
Ophiobolin C is a rare and high-purity compound distinguished by its intricate stereochemistry and unique molecular interactions. It demonstrates notable affinity for specific receptors, facilitating selective binding and modulation of biochemical pathways. The compound's reactivity is characterized by its ability to undergo rapid cyclization, leading to diverse reaction kinetics. Its exceptional purity ensures consistent performance in specialized environments, highlighting its intriguing chemical behavior and stability. | ||||||
Cyclopenin | 19553-26-5 | sc-202115 | 5 mg | $268.00 | ||
Cyclopenin is a rare and high-purity compound recognized for its distinctive structural features and unique reactivity as an acid halide. It exhibits selective electrophilic behavior, allowing for targeted interactions with nucleophiles. The compound's ability to form stable intermediates enhances its reaction kinetics, facilitating complex synthetic pathways. Its high purity contributes to reproducible results in experimental settings, showcasing its remarkable chemical stability and versatility. | ||||||
Enniatin B1 | 19914-20-6 | sc-202151 | 1 mg | $255.00 | 2 | |
Enniatin B1 is a rare and high-purity compound distinguished by its unique cyclic structure and specific molecular interactions. It demonstrates exceptional affinity for metal ions, leading to the formation of stable coordination complexes. This property influences its reactivity, allowing for selective pathways in organic synthesis. Additionally, Enniatin B1 exhibits notable solubility characteristics, enhancing its behavior in various solvent systems and contributing to its distinct chemical profile. | ||||||
Ostreogrycin A | 21411-53-0 | sc-202269 | 5 mg | $422.00 | ||
Ostreogrycin A is a rare and high-purity compound characterized by its intricate molecular architecture and unique reactivity as an acid halide. It engages in selective acylation reactions, showcasing distinct kinetic profiles that facilitate rapid transformations. Its ability to form transient intermediates enhances its role in catalytic cycles. Furthermore, Ostreogrycin A exhibits intriguing solvation dynamics, influencing its interactions in diverse chemical environments and contributing to its distinctive behavior. | ||||||
Virginiamycin S1 | 23152-29-6 | sc-202384 sc-202384A | 5 mg 25 mg | $379.00 $1275.00 | ||
Virginiamycin S1 is a rare and high-purity compound distinguished by its complex stereochemistry and unique reactivity patterns. It exhibits selective binding affinities, allowing for specific molecular interactions that influence reaction pathways. The compound's kinetic behavior is marked by its ability to stabilize reactive intermediates, enhancing its role in various chemical transformations. Additionally, Virginiamycin S1 demonstrates notable solubility characteristics, affecting its behavior in different solvent systems. | ||||||
Neoaureothin | 28900-27-8 | sc-202242 | 500 µg | $288.00 | ||
Neoaureothin is a rare and high-purity compound characterized by its intricate molecular architecture and distinctive reactivity as an acid halide. It showcases unique electrophilic properties, facilitating selective nucleophilic attacks that lead to diverse reaction pathways. The compound's stability under varying conditions allows for the formation of transient intermediates, influencing its kinetic profile. Furthermore, Neoaureothin exhibits exceptional solubility in polar solvents, enhancing its reactivity in specific environments. | ||||||
Aspercolorin | 29123-52-2 | sc-202067 | 1 mg | $188.00 | ||
Aspercolorin is a rare and high-purity acid halide distinguished by its unique steric configuration and reactivity. Its molecular structure promotes specific interactions with nucleophiles, enabling tailored reaction pathways that yield diverse products. The compound's high electrophilicity enhances its reactivity, while its ability to form stable complexes with various substrates influences reaction kinetics. Additionally, Aspercolorin demonstrates remarkable solubility in organic solvents, further expanding its reactivity profile. | ||||||