Items 291 to 294 of 294 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Hematin | 15489-90-4 | sc-207729 sc-207729A sc-207729D sc-207729C | 250 mg 1 g 100 g 10 g | $73.00 $80.00 $5728.00 $734.00 | 1 | |
Hematin is a heme derivative that exhibits unique coordination chemistry, particularly through its iron center, which can engage in diverse ligand interactions. Its ability to form stable complexes with various anions enhances its reactivity in electron transfer processes. Hematin's distinct electronic structure allows for specific redox reactions, influencing its kinetic behavior in catalytic cycles. Additionally, its solubility in organic solvents facilitates unique pathways in organic synthesis and material science. | ||||||
Copper(II) phthalocyanine | 147-14-8 | sc-214756 sc-214756A | 10 g 50 g | $45.00 $167.00 | ||
Copper(II) phthalocyanine is a robust coordination compound characterized by its extensive π-conjugated system, which imparts remarkable stability and vibrant coloration. Its planar structure allows for effective stacking interactions, enhancing its electronic properties. The compound exhibits unique photophysical behavior, including strong light absorption and fluorescence, making it a subject of interest in various applications. Its interactions with metal ions can lead to diverse catalytic pathways, influencing reaction kinetics and selectivity in various chemical processes. | ||||||
Tributyltin benzoate | 4342-36-3 | sc-500893 | 5 g | $250.00 | ||
Tributyltin benzoate is a versatile organotin compound known for its unique coordination chemistry and hydrophobic characteristics. Its tributyltin moiety enhances lipophilicity, facilitating interactions with biological membranes. The compound exhibits distinct reactivity patterns, particularly in nucleophilic substitution reactions, where it can act as a tin source. Additionally, its ability to form stable complexes with various ligands influences its behavior in catalysis and environmental chemistry, showcasing its multifaceted role in metal-organic frameworks. | ||||||
Lithium Aluminum Deuteride | 14128-54-2 | sc-488305 sc-488305A | 1 g 5 g | $550.00 $1650.00 | ||
Lithium Aluminum Deuteride is a notable metal hydride characterized by its unique deuterated structure, which enhances its reactivity in hydrogenation reactions. The compound exhibits strong ionic interactions, facilitating the transfer of deuteride ions in various chemical processes. Its low density and high thermal stability contribute to its effectiveness in reducing metal oxides. Additionally, the distinct kinetic pathways it follows in reactions highlight its role in synthetic chemistry, particularly in the formation of complex organometallic compounds. | ||||||