Items 261 to 270 of 387 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Ammonium tetraphenylborate | 14637-34-4 | sc-227261 | 10 g | $90.00 | ||
Ammonium tetraphenylborate is an intriguing organometallic compound known for its unique tetrahedral geometry, where a central boron atom is coordinated by four phenyl groups. This structure promotes significant steric hindrance and electronic effects, influencing its solubility and reactivity. The compound exhibits interesting ion-pairing dynamics, which can affect its interactions in various solvents, and it plays a role in stabilizing reactive intermediates in organometallic chemistry. | ||||||
Isopropoxytrimethylsilane | 1825-64-5 | sc-228374 | 10 ml | $71.00 | ||
Isopropoxytrimethylsilane is a notable organometallic compound characterized by its silane backbone, which facilitates unique reactivity patterns in organosilicon chemistry. Its isopropoxy groups enhance solubility in organic solvents and promote specific molecular interactions, particularly in nucleophilic substitution reactions. The compound exhibits distinct kinetic behavior, often accelerating reactions through the formation of stable intermediates, making it a key player in various synthetic pathways. | ||||||
Tetrarhodium dodecacarbonyl | 19584-30-6 | sc-251217 | 250 mg | $220.00 | ||
Tetrarhodium dodecacarbonyl is a fascinating organometallic complex known for its unique cluster structure, which allows for intriguing metal-metal interactions. This compound exhibits remarkable stability and reactivity, particularly in carbonylation reactions, where it can facilitate the formation of carbon-carbon bonds. Its ability to engage in oxidative addition and reductive elimination pathways enhances its role in catalysis, showcasing distinct kinetic profiles that are influenced by ligand dynamics and metal coordination. | ||||||
Diphenyl ditelluride | 32294-60-3 | sc-234777 | 1 g | $41.00 | ||
Diphenyl ditelluride is an intriguing organometallic compound characterized by its unique tellurium-sulfur interactions, which contribute to its distinctive reactivity. This compound exhibits notable electron-donating properties, facilitating nucleophilic attacks in various chemical transformations. Its ability to participate in redox reactions and form stable intermediates highlights its role in organometallic chemistry. Additionally, the steric effects of the phenyl groups influence its reaction kinetics, making it a subject of interest in synthetic pathways. | ||||||
Dichlorodiisopropylsilane | 7751-38-4 | sc-252700 | 5 ml | $93.00 | ||
Dichlorodiisopropylsilane is a notable organometallic compound distinguished by its unique silicon-chlorine bond dynamics, which enhance its reactivity in various chemical environments. The steric bulk of the isopropyl groups imparts significant influence on its coordination chemistry, allowing for selective interactions with nucleophiles. This compound also exhibits interesting hydrolytic behavior, leading to the formation of silanol derivatives, which can further participate in condensation reactions, showcasing its versatility in synthetic applications. | ||||||
Dilongifolylborane | 77882-24-7 | sc-252726 | 5 g | $315.00 | ||
Dilongifolylborane is an intriguing organometallic compound characterized by its unique boron-carbon interactions, which facilitate distinct reactivity patterns in organoboron chemistry. Its structural framework allows for effective coordination with various ligands, promoting selective pathways in cross-coupling reactions. Additionally, the compound exhibits notable stability under ambient conditions, while its electrophilic nature enables efficient participation in nucleophilic attack mechanisms, enhancing its utility in synthetic transformations. | ||||||
1,7-Dichloro-octamethyltetrasiloxane | 2474-02-4 | sc-229834 | 25 g | $129.00 | ||
1,7-Dichloro-octamethyltetrasiloxane is a distinctive organometallic compound known for its unique siloxane backbone, which imparts flexibility and enhances molecular interactions. Its chlorinated structure facilitates specific electrophilic reactions, allowing for selective functionalization. The compound's ability to form stable complexes with various substrates promotes unique reaction pathways, while its low viscosity and high thermal stability contribute to its versatility in diverse chemical environments. | ||||||
4-Bromo-N,N-bis(trimethylsilyl)aniline | 5089-33-8 | sc-232494 | 5 ml | $68.00 | ||
4-Bromo-N,N-bis(trimethylsilyl)aniline is an intriguing organometallic compound characterized by its robust silyl groups, which enhance its nucleophilicity and facilitate unique coordination with metal centers. The presence of the bromine atom introduces distinct electrophilic properties, enabling selective substitution reactions. Its steric bulk and electronic effects influence reaction kinetics, promoting efficient pathways in cross-coupling and other transformations, while its solubility in organic solvents enhances its reactivity in diverse chemical systems. | ||||||
Ferrocenium hexafluorophosphate | 11077-24-0 | sc-257528 | 5 g | $240.00 | ||
Ferrocenium hexafluorophosphate is a notable organometallic compound distinguished by its stable cationic structure, which arises from the oxidation of ferrocene. This compound exhibits strong electrochemical properties, facilitating rapid electron transfer processes. Its unique interactions with various anions can lead to distinct reactivity patterns, influencing reaction mechanisms. Additionally, the compound's high solubility in polar solvents enhances its utility in redox chemistry and catalysis, showcasing its dynamic behavior in diverse chemical environments. | ||||||
Diphenyl(trimethylsilyl)phosphine | 17154-34-6 | sc-227922 | 1 g | $43.00 | ||
Diphenyl(trimethylsilyl)phosphine is an intriguing organometallic compound characterized by its unique phosphine functionality, which enhances its nucleophilicity and reactivity in various coupling reactions. The presence of trimethylsilyl groups significantly influences steric and electronic properties, allowing for selective interactions with electrophiles. Its ability to stabilize transition states and intermediates makes it a valuable participant in organophosphorus chemistry, facilitating diverse synthetic pathways and enhancing reaction kinetics. |