Silicon Compounds
Items 91 to 100 of 379 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Allyltrimethylsilane | 762-72-1 | sc-233844 | 10 g | $88.00 | ||
Allyltrimethylsilane is a silicon compound characterized by its unique allyl group, which enhances its reactivity in nucleophilic substitution reactions. The presence of trimethylsilyl groups provides steric protection, allowing for selective functionalization. Its ability to form stable silane intermediates plays a crucial role in facilitating cross-coupling reactions. Furthermore, the compound exhibits notable volatility and low viscosity, promoting efficient mixing in various chemical processes. | ||||||
Diethoxy(methyl)phenylsilane | 775-56-4 | sc-234623 | 10 ml | $41.00 | ||
Diethoxy(methyl)phenylsilane is a silicon compound distinguished by its diethoxy and methyl groups, which enhance its solubility and reactivity in condensation reactions. The phenyl group contributes to its electronic properties, allowing for unique π-π interactions that can stabilize transition states. This compound exhibits a propensity for hydrolysis, forming silanol derivatives, which can further engage in siloxane bond formation, influencing polymerization pathways and material properties. | ||||||
Methyldiphenylsilane | 776-76-1 | sc-295474 | 25 ml | $139.00 | ||
Methyldiphenylsilane is a silicon compound characterized by its unique diphenyl structure, which facilitates strong π-π stacking interactions, enhancing its stability in various chemical environments. Its methyl group contributes to steric hindrance, influencing reaction kinetics and selectivity in cross-coupling reactions. The compound's reactivity with electrophiles is notable, allowing for diverse functionalization pathways, while its hydrophobic nature aids in phase separation in complex mixtures. | ||||||
Dimethyldiphenylsilane | 778-24-5 | sc-234755 | 5 g | $68.00 | ||
Dimethyldiphenylsilane is a silicon compound distinguished by its dual methyl substituents, which enhance its solubility and reactivity in organic solvents. The presence of diphenyl groups promotes significant steric effects, influencing molecular interactions and reactivity profiles. This compound exhibits unique coordination behavior with metal catalysts, facilitating efficient pathways in organometallic reactions. Its hydrophobic characteristics also contribute to its role in modifying surface properties in various applications. | ||||||
Tripropylsilane | 998-29-8 | sc-229620 | 5 g | $43.00 | ||
Tripropylsilane is a silicon compound characterized by its three propyl groups, which impart notable hydrophobicity and enhance its compatibility with non-polar solvents. The branched structure leads to unique steric hindrance, affecting its reactivity in nucleophilic substitution reactions. Additionally, its ability to form stable siloxane linkages allows for versatile interactions in polymer synthesis, while its low volatility aids in maintaining reaction conditions in various chemical processes. | ||||||
Tributylsilane | 998-41-4 | sc-229553 | 10 g | $177.00 | ||
Tributylsilane is a silicon compound distinguished by its four butyl groups, which contribute to its significant hydrophobic character and enhance solubility in organic solvents. The compound exhibits unique reactivity due to its sterically hindered structure, influencing its behavior in cross-coupling reactions. Its capacity to form robust siloxane bonds facilitates the creation of complex silicate networks, while its low surface energy promotes effective adhesion in various applications. | ||||||
3-Cyanopropyltriethoxysilane | 1067-47-6 | sc-223536 sc-223536A | 25 g 100 g | $55.00 $135.00 | 1 | |
3-Cyanopropyltriethoxysilane is a silicon compound characterized by its triethoxysilane backbone and a cyanopropyl functional group, which introduces polar characteristics that enhance its reactivity. This compound exhibits unique interactions with moisture, leading to hydrolysis and subsequent silanol formation, which can promote siloxane bond creation. Its ability to form stable silicate networks and modify surface properties makes it a versatile agent in various chemical processes. | ||||||
Tris(trimethylsilyl)methane | 1068-69-5 | sc-258320 | 5 g | $304.00 | ||
Tris(trimethylsilyl)methane is a silicon compound notable for its unique steric and electronic properties, arising from the presence of three trimethylsilyl groups. This configuration imparts significant hydrophobicity and enhances its reactivity in nucleophilic substitution reactions. The compound can stabilize reactive intermediates, facilitating various synthetic pathways. Its ability to form robust siloxane linkages contributes to the development of complex silicate structures, making it a key player in materials science. | ||||||
Hexylsilane | 1072-14-6 | sc-224016 | 5 ml | $126.00 | ||
Hexylsilane is a silicon compound characterized by its linear alkyl chain, which influences its solubility and surface activity. The presence of the hexyl group enhances its ability to interact with organic substrates, promoting adhesion and compatibility in various systems. Its reactivity is marked by the formation of siloxane bonds, enabling the creation of diverse polymeric networks. Additionally, Hexylsilane exhibits unique thermal stability, making it suitable for high-performance applications. | ||||||
Triethylvinylsilane | 1112-54-5 | sc-229575 | 5 g | $181.00 | ||
Triethylvinylsilane is a silicon compound distinguished by its vinyl group, which facilitates unique polymerization pathways, particularly in the formation of siloxane networks. This compound exhibits notable reactivity due to its ability to undergo hydrosilylation and cross-linking reactions, enhancing material properties. Its triethyl groups contribute to its hydrophobic character, influencing interactions with various substrates and enhancing compatibility in silicone-based formulations. | ||||||