Items 61 to 70 of 381 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
2,2,4,4,6,6-Hexamethylcyclotrisilazane | 1009-93-4 | sc-223462 sc-223462A | 1 ml 10 ml | $27.00 $141.00 | ||
2,2,4,4,6,6-Hexamethylcyclotrisilazane is a silicon compound notable for its cyclic structure, which imparts unique conformational flexibility. The presence of bulky methyl groups enhances steric hindrance, influencing its reactivity and interaction with other molecules. This compound exhibits interesting coordination chemistry, allowing it to form stable complexes with various ligands. Its thermal stability and resistance to oxidation make it a significant player in silicone polymerization processes. | ||||||
Tetraallyl orthosilicate | 1067-43-2 | sc-229387 sc-229387A | 10 g 50 g | $153.00 $607.00 | ||
Tetraallyl orthosilicate is a silicon compound characterized by its unique tetrafunctional structure, which facilitates diverse polymerization pathways. The presence of allyl groups enhances its reactivity, enabling rapid cross-linking and network formation. This compound exhibits interesting solubility properties, allowing it to interact effectively with various solvents. Its ability to undergo selective reactions under mild conditions makes it a versatile building block in silicon-based materials. | ||||||
Tris(trimethylsilyl)amine | 1586-73-8 | sc-229652 | 5 g | $51.00 | ||
Tris(trimethylsilyl)amine is a silicon compound notable for its unique ability to stabilize reactive intermediates through strong Si-N interactions. This compound exhibits a high degree of steric hindrance due to its bulky trimethylsilyl groups, which influences its reactivity and selectivity in nucleophilic substitution reactions. Its distinctive electronic properties allow it to act as a strong base, facilitating the formation of silicon-nitrogen bonds in various synthetic pathways. | ||||||
Methoxytrimethylsilane | 1825-61-2 | sc-255269 sc-255269A | 10 g 50 g | $64.00 $190.00 | ||
Methoxytrimethylsilane is a silicon compound characterized by its ability to enhance the reactivity of silanol groups through methoxy substitution. This compound exhibits unique hydrolytic stability, allowing it to participate in condensation reactions without rapid degradation. Its trimethylsilyl groups provide significant steric protection, influencing the kinetics of reactions involving siloxane formation. Additionally, the presence of the methoxy group enhances its compatibility with various organic solvents, broadening its utility in silicon-based chemistry. | ||||||
Hexaphenyldisiloxane | 1829-40-9 | sc-228298 | 5 g | $70.00 | ||
Hexaphenyldisiloxane is a silicon compound notable for its unique siloxane backbone, which features a high degree of phenyl substitution. This structure imparts exceptional thermal stability and low surface energy, making it resistant to oxidation and degradation. The compound exhibits interesting molecular interactions due to π-π stacking between phenyl groups, influencing its reactivity in polymerization processes. Its distinct viscosity and refractive index also make it a subject of interest in material science and nanotechnology. | ||||||
(3-Glycidyloxypropyl)triethoxysilane | 2602-34-8 | sc-231735 | 50 ml | $494.00 | ||
(3-Glycidyloxypropyl)triethoxysilane is a silicon compound characterized by its epoxy-functionalized silane structure, which facilitates strong covalent bonding with various substrates. This compound exhibits unique reactivity through its epoxy group, enabling cross-linking and enhancing adhesion properties in composite materials. Its triethoxy groups promote hydrolysis and condensation reactions, leading to the formation of robust siloxane networks. Additionally, its ability to modify surface properties makes it valuable in enhancing the durability and performance of coatings and adhesives. | ||||||
Trihexylsilane | 2929-52-4 | sc-237317 | 25 g | $208.00 | ||
Trihexylsilane is a silicon compound notable for its long hydrocarbon chains, which enhance its hydrophobic characteristics and promote unique interactions with organic materials. Its structure allows for effective silanization, improving surface energy and compatibility with various substrates. The compound exhibits interesting reaction kinetics, particularly in hydrolysis, leading to the formation of siloxane bonds that contribute to the stability and integrity of silane-modified surfaces. | ||||||
Tetrakis(trimethylsilyloxy)silane | 3555-47-3 | sc-237058 | 5 ml | $90.00 | ||
Tetrakis(trimethylsilyloxy)silane is a silicon compound characterized by its unique siloxy groups, which facilitate robust interactions with silicate surfaces. This compound exhibits remarkable reactivity, particularly in condensation reactions, leading to the formation of siloxane networks. Its high degree of silylation enhances thermal stability and promotes effective adhesion in various applications. The presence of multiple trimethylsilyloxy groups also contributes to its low surface energy, making it an effective modifier for diverse materials. | ||||||
N,N-Diethyl-1,1-dimethylsilylamine | 13686-66-3 | sc-228753 | 1 g | $111.00 | ||
N,N-Diethyl-1,1-dimethylsilylamine is a silicon compound notable for its unique amine-silicon interactions, which enhance its reactivity in nucleophilic substitution reactions. The presence of both ethyl and dimethyl groups contributes to its steric properties, influencing reaction kinetics and selectivity. This compound exhibits significant solubility in organic solvents, facilitating its use in various chemical syntheses. Its ability to form stable complexes with metal ions further underscores its versatility in coordination chemistry. | ||||||
(3-Mercaptopropyl)triethoxysilane | 14814-09-6 | sc-231785 | 25 ml | $198.00 | ||
(3-Mercaptopropyl)triethoxysilane is a silicon compound characterized by its thiol functional group, which enables strong interactions with metal surfaces and enhances adhesion properties. Its triethoxy groups facilitate hydrolysis, leading to silanol formation that promotes bonding with silicate substrates. The compound's unique structure allows for the formation of cross-linked networks, enhancing mechanical strength and durability in composite materials. Its reactivity with various substrates makes it a key player in surface modification processes. |