Items 301 to 310 of 381 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Silica Gel, 40-63 Micron Particles | 112926-00-8 | sc-220103 | 500 g | $305.00 | ||
Silica gel, featuring 40-63 micron particles, is a versatile silicon compound characterized by its extensive porosity and high surface area. This amorphous material exhibits unique adsorption dynamics, allowing it to selectively interact with a wide range of polar and non-polar substances. Its robust framework enhances mechanical strength, while the intricate pore structure facilitates rapid diffusion of gases and liquids, making it an effective medium for various physical processes. | ||||||
N,O-Bis(trimethylsilyl)carbamate | 35342-88-2 | sc-255384 | 10 g | $80.00 | ||
N,O-Bis(trimethylsilyl)carbamate is a silicon compound notable for its ability to form stable siloxane linkages, which enhances its reactivity in condensation reactions. Its trimethylsilyl groups provide steric hindrance, influencing reaction kinetics and selectivity in synthetic pathways. This compound exhibits unique solubility characteristics, allowing it to interact favorably with both polar and non-polar solvents, thus facilitating diverse chemical transformations. | ||||||
3-(Trimethylsilyl)-1-propanesulfonic acid sodium salt | 2039-96-5 | sc-238479 | 1 g | $77.00 | ||
3-(Trimethylsilyl)-1-propanesulfonic acid sodium salt is a silicon compound characterized by its strong acidity and unique ability to stabilize reactive intermediates through its trimethylsilyl groups. These groups enhance the compound's solubility in various solvents, promoting efficient ionization and facilitating nucleophilic attacks. Its distinct molecular structure allows for effective interactions with metal ions, influencing catalytic processes and reaction dynamics in synthetic chemistry. | ||||||
1-{3-Bromo-propyl)-4-[2-(tert-butyl-diphenyl-silanyloxy)ethyl]-piperazine | sc-333682 | 1 g | $638.00 | |||
1-{3-Bromo-propyl)-4-[2-(tert-butyl-diphenyl-silanyloxy)ethyl]-piperazine is a silicon compound notable for its robust siloxy linkage, which enhances its thermal stability and reactivity. The presence of the bromopropyl group introduces electrophilic characteristics, facilitating nucleophilic substitution reactions. Its unique piperazine framework contributes to conformational flexibility, allowing for diverse molecular interactions, which can influence reaction pathways and kinetics in various chemical environments. | ||||||
Chlorotribenzylsilane | 18740-59-5 | sc-239535 | 5 g | $403.00 | ||
Chlorotribenzylsilane is a silicon compound characterized by its triaryl silane structure, which imparts significant steric hindrance and electronic effects. The chlorinated silane exhibits strong reactivity due to the presence of the chlorobenzyl groups, promoting nucleophilic attack and facilitating cross-coupling reactions. Its unique molecular architecture allows for selective interactions with various substrates, influencing reaction kinetics and pathways in organosilicon chemistry. | ||||||
Trichloro(octyl)silane | 5283-66-9 | sc-237274 | 100 g | $60.00 | ||
Trichloro(octyl)silane is a silicon compound distinguished by its octyl chain, which enhances hydrophobicity and influences surface interactions. The presence of three chlorine atoms contributes to its reactivity, enabling it to participate in hydrolysis and condensation reactions. This compound's unique structure facilitates the formation of siloxane bonds, promoting the development of silane networks. Its behavior in polymerization processes showcases its potential for modifying surface properties and enhancing adhesion in various applications. | ||||||
Chlorotrihexylsilane | 3634-67-1 | sc-234348 | 5 g | $50.00 | ||
Chlorotrihexylsilane is a silicon compound characterized by its hexyl chains, which impart unique hydrophobic properties and alter molecular interactions at interfaces. The three chlorine substituents enhance its reactivity, allowing for rapid hydrolysis and subsequent siloxane bond formation. This compound exhibits distinct reaction kinetics, facilitating the creation of robust silane networks. Its structural attributes enable effective surface modification, influencing adhesion and compatibility in diverse chemical environments. | ||||||
Trimethylsilyl-L-(+)-rhamnose | 108392-01-4 | sc-281178 | 500 mg | $57.00 | ||
Trimethylsilyl-L-(+)-rhamnose is a silicon compound notable for its unique stereochemistry and the presence of a trimethylsilyl group, which enhances its solubility in organic solvents. This compound exhibits interesting molecular interactions due to its sugar moiety, allowing for specific hydrogen bonding and steric effects. Its reactivity is influenced by the silicon atom, promoting efficient nucleophilic substitutions and facilitating the formation of siloxane linkages, which can lead to diverse polymeric structures. | ||||||
Tetrabutyl orthosilicate | 4766-57-8 | sc-474629 | 100 g | $106.00 | ||
Tetrabutyl orthosilicate is a silicon compound characterized by its four butyl groups, which enhance its hydrophobic properties and solubility in organic solvents. This compound exhibits unique reactivity, particularly in sol-gel processes, where it hydrolyzes to form siloxane networks. Its molecular structure allows for significant steric hindrance, influencing reaction kinetics and promoting selective interactions with various substrates, making it a versatile precursor in materials science. | ||||||
(Triphenylsilyl)acetylene | 6229-00-1 | sc-237366 | 5 g | $156.00 | ||
Triphenylsilylacetylene is a silicon compound distinguished by its triphenylsilyl group, which imparts notable electronic properties and steric effects. This compound engages in unique π-π stacking interactions due to its acetylenic structure, facilitating distinct pathways in cross-coupling reactions. Its reactivity is influenced by the presence of the silyl group, enhancing nucleophilicity and enabling selective functionalization, making it an intriguing subject for studies in organosilicon chemistry. |