Items 21 to 30 of 381 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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1-Trimethylsilyl-1,2,4-triazole | 18293-54-4 | sc-264976 | 5 g | $95.00 | ||
1-Trimethylsilyl-1,2,4-triazole is a silicon compound notable for its ability to enhance the stability of reactive intermediates through unique silicon-nitrogen interactions. Its trimethylsilyl group provides steric protection, influencing reaction kinetics and selectivity in various chemical transformations. This compound exhibits a propensity for forming stable complexes with metal ions, which can alter catalytic pathways and improve reaction efficiencies in synthetic applications. | ||||||
Octadecylsilane | 18623-11-5 | sc-228872 | 25 g | $123.00 | ||
Octadecylsilane is a silicon compound characterized by its long hydrophobic alkyl chain, which significantly influences surface properties and molecular interactions. This compound forms self-assembled monolayers, enhancing surface hydrophobicity and reducing surface energy. Its unique silane functionality allows for strong covalent bonding to various substrates, facilitating tailored surface modifications. Additionally, the compound exhibits distinct thermal stability, making it suitable for diverse applications in material science. | ||||||
Chlorotrimethylsilane | 75-77-4 | sc-294014 sc-294014A | 250 ml 1 L | $41.00 $102.00 | ||
Chlorotrimethylsilane is a silicon compound notable for its reactivity as a silylating agent. It readily participates in nucleophilic substitution reactions, enabling the introduction of trimethylsilyl groups into organic molecules. This compound exhibits a high degree of volatility and low viscosity, which can influence reaction kinetics and facilitate rapid silylation processes. Its ability to form stable siloxane bonds enhances the durability of modified materials, making it a key player in organosilicon chemistry. | ||||||
Fluorotriphenylsilane | 379-50-0 | sc-263335 | 5 g | $116.00 | ||
Fluorotriphenylsilane is a silicon compound distinguished by its unique fluorinated structure, which enhances its electrophilic character. This compound engages in selective reactions with nucleophiles, leading to the formation of stable silane derivatives. Its bulky triphenyl groups contribute to steric hindrance, influencing reaction pathways and kinetics. Additionally, the presence of fluorine atoms imparts distinctive physical properties, such as increased thermal stability and altered solubility profiles, making it a versatile reagent in silicon chemistry. | ||||||
Trimethoxy(3,3,3-trifluoropropyl)silane | 429-60-7 | sc-237333 | 5 g | $100.00 | ||
Trimethoxy(3,3,3-trifluoropropyl)silane is a silicon compound characterized by its trifluoropropyl group, which significantly enhances its reactivity and surface adhesion properties. The presence of three methoxy groups facilitates hydrolysis, promoting the formation of silanol species that can bond with various substrates. This compound exhibits unique interaction dynamics due to the electronegative fluorine atoms, which influence its polarity and compatibility with organic materials, making it a noteworthy candidate in surface modification and polymer chemistry. | ||||||
Hexamethylcyclotrisiloxane | 541-05-9 | sc-235302 | 25 g | $23.00 | ||
Hexamethylcyclotrisiloxane is a cyclic siloxane featuring a unique arrangement of silicon and oxygen atoms that imparts distinct properties. Its structure allows for flexible molecular interactions, enabling it to act as a versatile intermediate in polymer synthesis. The compound exhibits low viscosity and high thermal stability, facilitating its use in various chemical processes. Additionally, its ability to undergo ring-opening polymerization highlights its significance in creating siloxane-based materials with tailored characteristics. | ||||||
Methyltriphenylsilane | 791-29-7 | sc-269605 | 1 g | $33.00 | ||
Methyltriphenylsilane is a silane compound characterized by its triphenylsilane backbone, which enhances its reactivity and solubility in organic solvents. This compound exhibits unique steric effects due to the bulky phenyl groups, influencing its interaction with nucleophiles and electrophiles. Its ability to participate in hydrosilylation reactions and form stable siloxane linkages makes it a key player in the synthesis of advanced materials, showcasing its role in modifying surface properties and enhancing adhesion. | ||||||
1,1,2,2-Tetramethyldisilane | 814-98-2 | sc-224861 | 1 g | $146.00 | ||
1,1,2,2-Tetramethyldisilane is a silicon compound notable for its unique structural arrangement, featuring two silicon atoms bonded to four methyl groups. This configuration imparts significant steric hindrance, affecting its reactivity and interaction with other chemical species. The compound exhibits a propensity for forming siloxane bonds, facilitating cross-linking in polymer matrices. Its low viscosity and high volatility enhance its utility in chemical vapor deposition processes, promoting uniform film formation on substrates. | ||||||
Trimethylhydroxysilane | 1066-40-6 | sc-264473 sc-264473A | 1 g 5 g | $31.00 $84.00 | ||
Trimethylhydroxysilane is a silicon compound characterized by its hydroxyl functional group attached to a trimethylsilane structure. This configuration allows for strong hydrogen bonding interactions, enhancing its reactivity in condensation reactions. The presence of the hydroxyl group facilitates the formation of siloxane linkages, promoting network formation in silicate materials. Additionally, its unique molecular geometry contributes to its role as a versatile precursor in the synthesis of siloxane polymers and coatings. | ||||||
1,1,2,2-Tetramethyl-1,2-diphenyldisilane | 1145-98-8 | sc-264995 | 1 g | $106.00 | ||
1,1,2,2-Tetramethyl-1,2-diphenyldisilane is a silicon compound notable for its unique silane structure, which features bulky tetramethyl and diphenyl groups. This configuration imparts steric hindrance, influencing its reactivity and stability in various chemical environments. The compound exhibits interesting coordination chemistry, allowing it to form stable complexes with metal catalysts. Its distinct molecular interactions facilitate selective reactions, making it a valuable intermediate in silicon-based material synthesis. |