Items 71 to 80 of 387 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Octamethyltrisiloxane | 107-51-7 | sc-250611 | 5 ml | $35.00 | ||
Octamethyltrisiloxane is an organometallic compound characterized by its extended siloxane framework, which enables unique conformational flexibility and enhanced molecular interactions. This flexibility allows for effective solvation and stabilization of reactive intermediates, influencing reaction kinetics. Its low viscosity and high thermal stability facilitate the formation of complex siloxane networks, while its ability to engage in hydrophobic interactions enhances compatibility with various substrates, promoting diverse chemical pathways. | ||||||
Triethyl borate | 150-46-9 | sc-251319 | 100 ml | $65.00 | ||
Triethyl borate is an organometallic compound notable for its ability to form strong Lewis acid interactions due to the presence of boron. This property allows it to effectively coordinate with nucleophiles, facilitating various reaction pathways. Its volatility and low viscosity contribute to rapid diffusion in reaction mixtures, enhancing kinetic rates. Additionally, the compound exhibits unique reactivity with alcohols, leading to the formation of esters and influencing polymerization processes. | ||||||
Decamethylcyclopentasiloxane | 541-02-6 | sc-239652 | 50 ml | $24.00 | ||
Decamethylcyclopentasiloxane is an organometallic compound characterized by its unique siloxane backbone, which imparts flexibility and low surface tension. This structure enables it to engage in distinctive molecular interactions, particularly with polar solvents, enhancing solubility and compatibility in various systems. Its low viscosity promotes efficient mass transfer, while its ability to form stable complexes with metal ions can influence catalytic processes and reaction kinetics, making it a versatile component in synthetic pathways. | ||||||
Tetrapropyl orthosilicate | 682-01-9 | sc-251212 | 25 g | $39.00 | ||
Tetrapropyl orthosilicate is an organometallic compound notable for its tetrahedral geometry, which facilitates unique coordination interactions with metal centers. This structure enhances its reactivity in sol-gel processes, promoting the formation of silicate networks. Its ability to hydrolyze in the presence of moisture leads to the generation of silanol groups, influencing polymerization kinetics and network formation. Additionally, its low volatility and high reactivity make it a key player in surface modification and material synthesis. | ||||||
Trimethyl(phenyl)silane | 768-32-1 | sc-251355 | 25 g | $112.00 | ||
Trimethyl(phenyl)silane is an organometallic compound characterized by its unique silane structure, which allows for versatile bonding interactions with various substrates. Its sterically hindered nature influences reaction pathways, promoting selective reactivity in cross-coupling reactions. The compound exhibits distinct electronic properties due to the presence of the phenyl group, enhancing its role in catalysis and facilitating the formation of stable intermediates. Its hydrophobic characteristics also contribute to its behavior in organic synthesis, affecting solubility and reactivity profiles. | ||||||
Methylmagnesium iodide solution | 917-64-6 | sc-295478 | 100 g | $238.00 | ||
Methylmagnesium iodide solution is a highly reactive organometallic compound known for its strong nucleophilic properties. It readily engages in Grignard reactions, facilitating the formation of carbon-carbon bonds through its ability to donate a methyl group. The presence of iodine enhances its reactivity, allowing for rapid interactions with electrophiles. Its polar nature influences solubility in organic solvents, while its reactivity with moisture underscores the importance of anhydrous conditions in synthetic applications. | ||||||
n-Butyltrimethoxysilane | 1067-57-8 | sc-286396 sc-286396A | 5 g 25 g | $135.00 $175.00 | ||
n-Butyltrimethoxysilane is a versatile organosilane that exhibits unique reactivity due to its trimethoxy functional groups. These groups can undergo hydrolysis, leading to the formation of silanol species that promote siloxane bond formation. This compound demonstrates significant surface adhesion properties, enhancing the compatibility of organic materials with inorganic substrates. Its ability to form stable siloxane networks contributes to its utility in modifying surface characteristics and improving material durability. | ||||||
Triethoxymethylsilane | 2031-67-6 | sc-251317 | 50 g | $29.00 | ||
Triethoxymethylsilane is an organosilane characterized by its triethoxy groups, which facilitate hydrolysis and subsequent condensation reactions. This process generates reactive silanol intermediates, enabling the formation of robust siloxane linkages. The compound's unique reactivity allows for tailored surface modifications, enhancing interfacial adhesion and promoting the integration of organic and inorganic materials. Its ability to create cross-linked networks contributes to improved mechanical properties and environmental resistance in various applications. | ||||||
2,4,6,8-Tetramethylcyclotetrasiloxane | 2370-88-9 | sc-251856 sc-251856A sc-251856B sc-251856C | 25 ml 100 ml 500 ml 1 L | $187.00 $300.00 $900.00 $1800.00 | ||
2,4,6,8-Tetramethylcyclotetrasiloxane is a cyclic siloxane that exhibits unique molecular interactions due to its tetrahedral symmetry and flexible structure. This compound can undergo ring-opening polymerization, leading to the formation of siloxane polymers with tunable properties. Its low viscosity and high thermal stability facilitate efficient processing, while its distinct reactivity allows for the incorporation of various functional groups, enhancing compatibility with diverse substrates and applications. | ||||||
Vinyltrimethoxysilane | 2768-02-7 | sc-251431 sc-251431A | 100 ml 500 ml | $57.00 $161.00 | ||
Vinyltrimethoxysilane is an organosilane that showcases remarkable reactivity through its vinyl group, enabling it to participate in various polymerization processes. Its ability to form siloxane bonds enhances adhesion to inorganic surfaces, promoting cross-linking in composite materials. The compound's unique structure allows for selective interactions with moisture, facilitating hydrolysis and subsequent condensation reactions, which contribute to the formation of robust silane networks. |