Items 91 to 100 of 296 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Tricyclohexyltin chloride | 3091-32-5 | sc-237284 | 5 g | $136.00 | ||
Tricyclohexyltin chloride is an organotin compound distinguished by its unique steric and electronic properties. The bulky cyclohexyl groups confer significant steric hindrance, influencing its reactivity in nucleophilic attack scenarios. This compound exhibits a propensity for forming stable complexes with various ligands, facilitating distinct coordination chemistry. Its chloride moiety enhances its reactivity, allowing for selective pathways in organometallic transformations, making it a subject of interest in synthetic applications. | ||||||
Tributyl(phenylethynyl)tin | 3757-88-8 | sc-237260 | 5 g | $300.00 | ||
Tributyl(phenylethynyl)tin is an organotin compound characterized by its unique phenylethynyl group, which introduces distinct electronic properties and enhances its reactivity. The presence of three butyl groups provides significant steric bulk, influencing its interaction with nucleophiles and electrophiles. This compound exhibits notable coordination behavior, forming stable organometallic complexes that can facilitate diverse reaction pathways, making it a subject of interest in advanced materials chemistry. | ||||||
Copper (II) acetate monohydrate | 6046-93-1 | sc-203008A sc-203008 sc-203008B sc-203008C | 100 g 500 g 2.5 kg 5 kg | $24.00 $85.00 $177.00 $250.00 | ||
Copper (II) acetate monohydrate is a coordination compound featuring copper ions that engage in dynamic interactions with acetate ligands. Its crystalline structure allows for hydrogen bonding with water molecules, influencing solubility and reactivity. The compound exhibits unique redox properties, facilitating electron transfer processes. Additionally, its ability to form complexes with various substrates enhances its role in catalysis, showcasing its versatility in chemical transformations. | ||||||
Tributyltin iodide | 7342-47-4 | sc-237271 | 10 g | $67.00 | ||
Tributyltin iodide is a complex organotin compound characterized by its unique tin-carbon bond interactions, which enhance its reactivity in nucleophilic substitution reactions. The presence of bulky butyl groups imparts steric hindrance, influencing reaction kinetics and selectivity. This compound exhibits significant lipophilicity, allowing it to interact with various organic substrates. Its ability to form stable organotin complexes further underscores its role in diverse chemical pathways, particularly in organometallic chemistry. | ||||||
Tetraallyltin | 7393-43-3 | sc-253650 | 5 g | $143.00 | ||
Tetraallyltin is an organotin compound notable for its distinctive tetrahedral geometry, which facilitates unique coordination with various ligands. The presence of four allyl groups enhances its reactivity, allowing for rapid participation in cross-coupling reactions. Its electron-rich nature promotes strong π-π stacking interactions, influencing its behavior in polymerization processes. Additionally, Tetraallyltin exhibits significant volatility, making it a subject of interest in studies of organometallic reactivity and stability. | ||||||
Platinum Sponge, 60 Mesh | 7440-06-4 | sc-396747 sc-396747A | 1 g 5 g | $535.00 $2150.00 | ||
Platinum Sponge, 60 Mesh, is a finely divided form of platinum characterized by its high surface area, which enhances catalytic activity in various reactions. Its porous structure allows for efficient gas adsorption and diffusion, facilitating unique electron transfer processes. The material exhibits remarkable stability under oxidative conditions, making it ideal for applications requiring robust performance. Additionally, its ability to form strong metal-ligand interactions contributes to its effectiveness in catalyzing hydrogenation and oxidation reactions. | ||||||
Nickel(II) chloride anhydrous | 7718-54-9 | sc-394490 | 25 g | $54.00 | ||
Nickel(II) chloride anhydrous is a hygroscopic compound that exhibits distinctive coordination chemistry, forming complexes with various ligands. Its crystalline structure allows for significant ionic interactions, influencing solubility and reactivity in different solvents. The compound participates in redox reactions, showcasing its ability to act as both an oxidizing and reducing agent. Additionally, its thermal stability and ability to form nickel complexes make it a key player in various synthetic pathways. | ||||||
Bis(dibutylchlorotin(IV)) oxide | 10428-19-0 | sc-223819 | 10 g | $115.00 | ||
Bis(dibutylchlorotin(IV)) oxide is a versatile organotin compound characterized by its unique organometallic interactions. It exhibits significant coordination behavior, forming stable complexes with various ligands, which enhances its reactivity. The compound's distinct steric and electronic properties influence its behavior in polymerization processes and catalysis. Its ability to undergo hydrolysis and form tin oxides further highlights its role in environmental chemistry and material science. | ||||||
Neodymium sulfide | 12035-32-4 | sc-394307 | 25 g | $719.00 | ||
Neodymium sulfide is a fascinating metal sulfide known for its unique electronic and optical properties. It exhibits strong covalent bonding, leading to distinct semiconductor behavior. The compound's crystal structure allows for effective charge carrier mobility, making it a subject of interest in photonic applications. Additionally, its interactions with light can result in luminescent phenomena, showcasing its potential in advanced materials research and optoelectronic devices. | ||||||
Magnesium nitrate hexahydrate | 13446-18-9 | sc-203127 sc-203127A sc-203127B sc-203127C sc-203127D sc-203127E | 100 g 500 g 1 kg 2.5 kg 5 kg 10 kg | $31.00 $82.00 $158.00 $223.00 $379.00 $551.00 | 1 | |
Magnesium nitrate hexahydrate is a versatile compound characterized by its hygroscopic nature and ability to form stable complexes with various ligands. Its crystalline structure facilitates ionic interactions, enhancing solubility in water. The compound participates in exothermic reactions, releasing heat upon dissolution, which can influence reaction kinetics in various chemical processes. Additionally, its role as a source of magnesium ions makes it significant in coordination chemistry and materials synthesis. |