Items 81 to 90 of 381 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane | 69304-37-6 | sc-251584 | 1 g | $58.00 | ||
1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane is a silicon compound notable for its dual chlorinated siloxane structure, which enhances its reactivity in condensation and substitution reactions. The presence of isopropyl groups contributes to steric hindrance, influencing reaction kinetics and selectivity. Its unique molecular configuration allows for versatile interactions with various nucleophiles, facilitating the formation of siloxane linkages and promoting the development of advanced materials with tailored properties. | ||||||
Methoxy(dimethyl)octylsilane | 93804-29-6 | sc-235619 | 5 g | $62.00 | ||
Methoxy(dimethyl)octylsilane is a silicon compound characterized by its unique silane structure, which features a long hydrophobic octyl chain. This configuration enhances its compatibility with organic materials, promoting strong interfacial adhesion. The methoxy and dimethyl groups facilitate hydrolysis, leading to the formation of silanol species that can engage in further polymerization. Its distinct molecular interactions enable the creation of robust siloxane networks, enhancing material durability and performance in various applications. | ||||||
1H,1H,2H,2H-Perfluorodecyltriethoxysilane | 101947-16-4 | sc-259052 sc-259052A | 1 g 5 g | $61.00 $127.00 | ||
1H,1H,2H,2H-Perfluorodecyltriethoxysilane is a silicon compound distinguished by its perfluorinated alkyl chain, which imparts exceptional hydrophobicity and oleophobicity. This unique structure promotes strong surface modification, enhancing resistance to moisture and chemical attack. The triethoxysilane groups facilitate rapid hydrolysis, forming reactive silanol intermediates that can bond with various substrates, leading to durable siloxane linkages and improved surface properties. | ||||||
Bis(methyldifluorosilyl)ethane | 170381-99-4 | sc-357421 sc-357421A | 1 g 5 g | $130.00 $96.00 | ||
Bis(methyldifluorosilyl)ethane is a silicon compound characterized by its unique difluorosilyl groups, which enhance its reactivity and interaction with various substrates. The presence of methyldifluorosilyl moieties allows for selective bonding and modification of surfaces, promoting unique chemical pathways. Its ability to form stable siloxane networks through condensation reactions contributes to its effectiveness in creating robust coatings, while its distinct molecular structure influences reaction kinetics and compatibility with diverse materials. | ||||||
1,1,3,3,5,5-Hexamethyl-1,5-bis[2-(5-norbornen-2-yl)ethyl]trisiloxane | 307496-39-5 | sc-224867 | 1 ml | $50.00 | ||
1,1,3,3,5,5-Hexamethyl-1,5-bis[2-(5-norbornen-2-yl)ethyl]trisiloxane is a silicon compound notable for its intricate trisiloxane framework, which facilitates unique molecular interactions. The presence of norbornene groups enables efficient cross-linking and polymerization, enhancing material properties. Its distinctive siloxane bonds contribute to thermal stability and flexibility, while the steric effects of the hexamethyl substituents influence reactivity and compatibility with various chemical environments. | ||||||
Sodium dimethylphenylsilanolate | sc-301817 | 1 g | $80.00 | |||
Sodium dimethylphenylsilanolate is a silicon compound characterized by its unique silanol functionality, which promotes strong hydrogen bonding and enhances reactivity with various substrates. The dimethyl and phenyl groups provide steric hindrance, influencing the compound's interaction dynamics and solubility in organic solvents. Its ability to act as a nucleophile allows for diverse reaction pathways, facilitating the formation of siloxane linkages and contributing to the development of advanced materials with tailored properties. | ||||||
Dodecamethylpentasiloxane | 141-63-9 | sc-227958 | 10 ml | $55.00 | ||
Dodecamethylpentasiloxane is a silicon compound notable for its extensive siloxane backbone, which imparts flexibility and low surface energy. This structure enables unique molecular interactions, such as van der Waals forces, enhancing its compatibility with various materials. Its high degree of methyl substitution contributes to hydrophobicity and thermal stability, while also influencing its viscosity and flow characteristics. These properties facilitate its role in modifying surface characteristics and improving material performance. | ||||||
Dimethoxy-methyl(3,3,3-trifluoropropyl)silane | 358-67-8 | sc-234714 | 5 g | $77.00 | ||
Dimethoxy-methyl(3,3,3-trifluoropropyl)silane is a silicon compound characterized by its trifluoropropyl group, which introduces significant polarity and enhances surface adhesion. The presence of methoxy groups allows for versatile reactivity, facilitating hydrolysis and condensation reactions. This compound exhibits unique interaction dynamics, promoting strong bonding with substrates while maintaining a low viscosity. Its distinct molecular architecture contributes to enhanced thermal stability and chemical resistance, making it suitable for various applications in material science. | ||||||
Diethylsilane | 542-91-6 | sc-257346 | 5 ml | $77.00 | ||
Diethylsilane is a silicon compound notable for its unique chain structure, which enhances its reactivity in hydrosilylation and cross-coupling reactions. The presence of ethyl groups contributes to its hydrophobic characteristics, influencing its interaction with organic substrates. This compound exhibits rapid reaction kinetics, facilitating the formation of siloxane bonds. Its low surface tension and ability to form stable emulsions make it an interesting candidate for applications requiring effective surface modification and enhanced material properties. | ||||||
Dimethylethylsilane | 758-21-4 | sc-257365 | 5 g | $102.00 | ||
Dimethylethylsilane is a silicon compound characterized by its branched structure, which promotes unique steric effects and influences its reactivity in various chemical processes. The presence of both methyl and ethyl groups enhances its compatibility with diverse organic molecules, facilitating selective reactions. This compound demonstrates significant volatility and low viscosity, which can affect its diffusion rates in reactions. Its ability to form stable siloxane networks underpins its utility in polymer synthesis and material science. |