Items 141 to 150 of 233 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Antibiotic TPU-0037-C | 485815-61-0 | sc-202060 | 500 µg | $250.00 | ||
Antibiotic TPU-0037-C is a rare and high-purity compound distinguished by its intricate molecular architecture and selective reactivity. Its unique functional groups facilitate specific intermolecular interactions, promoting distinct catalytic pathways. The compound exhibits remarkable solubility and a propensity for forming stable complexes, enhancing its kinetic behavior in diverse chemical environments. These characteristics render it a compelling candidate for exploring advanced reaction mechanisms and molecular behavior. | ||||||
Platensimycin | 835876-32-9 | sc-202292 | 250 µg | $462.00 | 1 | |
Platensimycin is a rare and high-purity compound characterized by its unique structural features and selective binding affinity. Its intricate arrangement of functional groups allows for specific interactions with target molecules, influencing reaction kinetics and pathways. The compound demonstrates exceptional stability in various solvents, promoting the formation of unique supramolecular assemblies. These properties make it an intriguing subject for studying molecular dynamics and complexation phenomena. | ||||||
Bischloroanthrabenzoxocinone | 866022-28-8 | sc-202079 | 500 µg | $349.00 | 2 | |
Bischloroanthrabenzoxocinone is a rare and high-purity compound distinguished by its unique electronic structure and reactivity as an acid halide. Its dual chlorinated aromatic system facilitates selective electrophilic interactions, enhancing its reactivity in condensation reactions. The compound exhibits remarkable solubility in polar solvents, which influences its aggregation behavior and potential for forming dynamic covalent bonds. These characteristics make it a fascinating candidate for exploring advanced synthetic methodologies and material science applications. | ||||||
Platencin | 869898-86-2 | sc-202291 | 100 µg | $612.00 | ||
Platencin is a rare and high-purity compound characterized by its intricate stereochemistry and unique reactivity profile as an acid halide. Its distinctive molecular framework allows for specific hydrogen bonding interactions, which can influence reaction pathways and kinetics. The compound's high polarity enhances its solvation properties, promoting effective intermolecular interactions. These features position Platencin as an intriguing subject for studies in advanced chemical synthesis and material properties. | ||||||
Deoxyviolacein | 5839-61-2 | sc-362730 sc-362730A | 500 µg 2.5 mg | $302.00 $1311.00 | ||
Deoxyviolacein is a rare and high-purity compound distinguished by its unique chromophoric structure, which facilitates intriguing electronic transitions and light absorption characteristics. Its ability to engage in selective π-π stacking interactions enhances its stability and reactivity in various environments. The compound's distinctive solubility profile and hydrophobic regions contribute to its behavior in complex mixtures, making it a fascinating subject for exploration in advanced chemical research and material science. | ||||||
Telomycin | 19246-24-3 | sc-202356 | 500 µg | $560.00 | ||
Telomycin is a rare and high-purity compound characterized by its unique structural framework that promotes specific hydrogen bonding interactions, influencing its reactivity and stability. Its distinct electron-donating and withdrawing groups facilitate complexation with metal ions, altering its electronic properties. Additionally, Telomycin exhibits remarkable solvation dynamics, which can affect its behavior in diverse chemical environments, making it an intriguing candidate for further investigation in advanced chemical studies. | ||||||
Luteoreticulin | 22388-89-2 | sc-202213 | 500 µg | $357.00 | ||
Luteoreticulin is a rare and high-purity compound distinguished by its intricate stereochemistry, which enhances its ability to engage in selective molecular interactions. Its unique functional groups enable it to participate in specific catalytic pathways, influencing reaction kinetics and product formation. The compound's exceptional solubility characteristics and stability under varying conditions further contribute to its intriguing behavior in complex chemical systems, warranting deeper exploration in research applications. | ||||||
Rugulosin (+ form) | 23537-16-8 | sc-202327 | 1 mg | $287.00 | 1 | |
Rugulosin is a rare and high-purity acid halide characterized by its unique reactivity profile and selective electrophilic nature. Its distinct carbonyl functionality facilitates rapid acylation reactions, allowing for precise modifications in organic synthesis. The compound exhibits remarkable stability in diverse solvents, promoting efficient interactions with nucleophiles. Additionally, its specific steric and electronic properties enable tailored reactivity, making it a subject of interest for advanced chemical studies. | ||||||
Pestalotin | 34565-32-7 | sc-202278 | 500 µg | $374.00 | ||
Pestalotin is a rare and high-purity acid halide known for its exceptional reactivity and specificity in chemical transformations. Its unique structural features promote selective interactions with various nucleophiles, leading to efficient acylation processes. The compound's distinctive electronic distribution enhances its electrophilic character, allowing for controlled reaction kinetics. Furthermore, Pestalotin's solubility in a range of solvents supports versatile applications in synthetic chemistry, making it a valuable subject for research. | ||||||
7-Hydroxypestalotin | 41164-59-4 | sc-202026 | 500 µg | $374.00 | ||
7-Hydroxypestalotin is a rare and high-purity acid halide distinguished by its unique ability to engage in selective molecular interactions. Its specific functional groups facilitate targeted reactivity with a variety of nucleophiles, promoting efficient acylation and esterification reactions. The compound exhibits notable stability under certain conditions, while its distinct electronic properties contribute to its electrophilic nature, enabling precise control over reaction pathways and kinetics in synthetic applications. | ||||||