Items 31 to 40 of 296 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Calcium | 7440-70-2 | sc-252536 | 5 g | $209.00 | ||
Calcium is a versatile alkaline earth metal known for its reactivity with nonmetals, particularly oxygen and halogens, forming stable ionic compounds. Its ability to donate electrons facilitates unique redox reactions, influencing various chemical pathways. The metal exhibits a distinct tendency to form alloys, enhancing its mechanical properties. Additionally, calcium's role in metallurgical processes is significant, as it acts as a reducing agent, promoting the extraction of other metals from their ores. | ||||||
Molybdenum dichloride dioxide | 13637-68-8 | sc-257803A sc-257803 | 1 g 10 g | $60.00 $300.00 | ||
Molybdenum dichloride dioxide is a transition metal compound characterized by its unique coordination chemistry and ability to form various oxidation states. It exhibits strong covalent bonding, leading to distinct electronic properties that influence its catalytic behavior. The compound participates in electron transfer processes, enhancing reaction kinetics in certain chemical transformations. Its layered structure allows for interesting intercalation phenomena, impacting its reactivity and stability in diverse environments. | ||||||
bpV(bipy) | sc-221376 sc-221376A | 5 mg 25 mg | $120.00 $280.00 | |||
bpV(bipy) is a phosphatase inhibitor that showcases remarkable coordination with metal ions, particularly through its bidentate ligand structure. This compound exhibits unique chelation properties, facilitating the formation of stable metal complexes. Its ability to modulate electron density around the metal center influences reaction pathways, enhancing selectivity in catalytic processes. Additionally, bpV(bipy) demonstrates intriguing solubility characteristics, affecting its interaction dynamics in various solvent systems. | ||||||
Mn-cpx 3 | sc-221951 | 25 mg | $399.00 | 1 | ||
Mn-cpx 3 is a versatile metal complex characterized by its unique ligand architecture, which promotes strong metal-ligand interactions. This compound exhibits distinct redox properties, allowing it to participate in electron transfer reactions with high efficiency. Its kinetic behavior is influenced by the steric and electronic effects of its ligands, leading to selective reactivity in various chemical environments. Furthermore, Mn-cpx 3 displays notable stability under diverse conditions, enhancing its utility in catalytic applications. | ||||||
Aluminum acetate, basic hydrate | 142-03-0 | sc-268495 sc-268495A | 100 g 500 g | $45.00 $140.00 | ||
Aluminum acetate, basic hydrate, is a unique coordination compound that showcases distinctive interactions between aluminum ions and acetate ligands. Its structure facilitates hydrogen bonding and electrostatic interactions, contributing to its solubility and reactivity in aqueous environments. The compound exhibits interesting hydrolysis behavior, leading to the formation of aluminum hydroxide species, which can influence pH levels in solution. Additionally, its ability to form complexes with various anions enhances its versatility in chemical processes. | ||||||
Manganese(II) Acetate, Anhydrous | 638-38-0 | sc-263454 | 50 g | $51.00 | ||
Manganese(II) Acetate, Anhydrous, is a notable coordination compound characterized by its ability to form stable complexes with various ligands. The manganese ions exhibit a distinct oxidation state that influences redox reactions, enhancing its reactivity. Its crystalline structure allows for unique lattice interactions, which can affect solubility and dissolution rates. Furthermore, the compound participates in catalytic pathways, facilitating electron transfer processes in organic synthesis. | ||||||
Hexaphenylditin(IV) | 1064-10-4 | sc-228299 | 5 g | $106.00 | ||
Hexaphenylditin(IV) is a unique organotin compound distinguished by its extensive phenyl substituents, which enhance its steric bulk and electronic properties. This configuration allows for intriguing molecular interactions, particularly in coordination chemistry, where it can form diverse organometallic complexes. Its reactivity is influenced by the tin center's oxidation state, enabling it to engage in nucleophilic substitution reactions. Additionally, the compound exhibits distinctive thermal stability and solubility characteristics, making it a subject of interest in materials science. | ||||||
Tetravinyltin | 1112-56-7 | sc-229445 | 5 g | $88.00 | ||
Tetravinyltin is a distinctive organotin compound that showcases unique reactivity patterns due to its tetravalent tin center. Its multiple vinyl groups enable efficient coordination with various substrates, promoting diverse polymerization mechanisms. The compound exhibits notable stability in radical reactions, influencing the kinetics of vinyl polymer formation. Additionally, its physical characteristics, such as solubility and viscosity, contribute to its intriguing behavior in materials science and polymer chemistry. | ||||||
Lead(II) methacrylate | 1068-61-7 | sc-269320 | 25 g | $129.00 | ||
Lead(II) methacrylate is a notable organolead compound characterized by its dual functionality as a metal and a methacrylate ester. Its unique structure facilitates strong coordination with various ligands, leading to interesting polymerization pathways. The compound exhibits significant reactivity due to the lead center's ability to participate in electron transfer processes, influencing its kinetics in radical polymerization. Additionally, its physical properties, such as density and refractive index, make it intriguing for applications in advanced materials. | ||||||
Trimethyl(phenylethynyl)tin | 1199-95-7 | sc-229591 | 1 g | $73.00 | ||
Trimethyl(phenylethynyl)tin is an intriguing organotin compound known for its distinctive reactivity and molecular interactions. The tin center exhibits a unique hybridization, allowing for effective π-π stacking with aromatic systems, which can influence the stability and reactivity of the compound. Its ability to form stable organometallic bonds enhances its role in cross-coupling reactions, while its hydrophobic nature contributes to its solubility in nonpolar solvents, facilitating diverse synthetic pathways. |