Items 11 to 20 of 387 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Bis(tributyltin) oxide | 56-35-9 | sc-252470B sc-252470C sc-252470 sc-252470A | 1 g 25 g 100 g 500 g | $30.00 $60.00 $150.00 $390.00 | ||
Bis(tributyltin) oxide is a notable organometallic compound distinguished by its ability to act as a Lewis acid, facilitating the formation of organotin intermediates. Its unique tin-oxygen bonding imparts significant stability, allowing for selective interactions with various substrates. The compound exhibits unique reactivity patterns, particularly in transmetalation processes, which can influence the kinetics of organometallic reactions and enable the synthesis of diverse organotin derivatives. | ||||||
Dibutyltin dilaurate | 77-58-7 | sc-239690 | 5 g | $37.00 | ||
Dibutyltin dilaurate is an organometallic compound characterized by its dual role as a catalyst and a reagent in polymerization reactions. Its structure allows for effective coordination with functional groups, enhancing reaction rates and selectivity. The compound exhibits unique reactivity through the formation of tin-alkyl bonds, which can facilitate the activation of electrophiles. This behavior contributes to its effectiveness in promoting various synthetic pathways, particularly in the production of polyurethanes. | ||||||
Triethoxyvinylsilane | 78-08-0 | sc-251318 | 100 ml | $33.00 | ||
Triethoxyvinylsilane is an organometallic compound notable for its ability to form siloxane bonds through hydrolysis and condensation reactions. Its vinyl group enables unique polymerization pathways, facilitating the creation of silane-terminated polymers. The compound's reactivity is influenced by the presence of ethoxy groups, which enhance its compatibility with various substrates. This versatility allows for tailored surface modifications and improved adhesion properties in composite materials. | ||||||
Trimethyltin hydroxide | 56-24-6 | sc-280157 | 1 g | $90.00 | ||
Trimethyltin hydroxide is an organometallic compound characterized by its strong Lewis acid properties, enabling it to engage in nucleophilic substitution reactions. Its trimethyl tin moiety enhances its reactivity, allowing for the formation of organotin derivatives through transmetalation processes. The compound exhibits unique solubility characteristics, facilitating interactions with polar and nonpolar solvents, which can influence reaction kinetics and pathways in organometallic synthesis. | ||||||
Triethoxy(ethyl)silane | 78-07-9 | sc-251316 | 50 ml | $62.00 | ||
Triethoxy(ethyl)silane is an organosilicon compound notable for its ability to form siloxane bonds through hydrolysis and condensation reactions. Its ethoxy groups enhance its reactivity, allowing for efficient grafting onto various substrates. The compound exhibits unique surface-active properties, promoting adhesion and compatibility with organic materials. Additionally, its molecular structure facilitates the formation of silane networks, influencing the mechanical and thermal stability of composite materials. | ||||||
Decamethyltetrasiloxane | 141-62-8 | sc-239653 | 25 g | $38.00 | ||
Decamethyltetrasiloxane is a siloxane compound characterized by its unique chain flexibility and low surface tension, which contribute to its exceptional wetting properties. Its molecular structure allows for effective interaction with both polar and non-polar surfaces, enhancing compatibility in diverse formulations. The compound's ability to undergo dynamic equilibrium in siloxane linkages facilitates unique reaction pathways, influencing polymerization kinetics and the formation of complex siloxane architectures. | ||||||
Propylmagnesium Bromide (ca. 27% in Tetrahydrofuran, ca. 2mol/L) | 927-77-5 | sc-301616 | 250 g | $213.00 | ||
Propylmagnesium Bromide is a Grignard reagent known for its strong nucleophilic character, enabling it to engage in rapid carbon-carbon bond formation. Its reactivity is influenced by the presence of the bromide ion, which enhances the electrophilic attack on carbonyl compounds. The organometallic nature allows for unique interactions with various substrates, leading to diverse synthetic pathways. Additionally, its solubility in tetrahydrofuran promotes efficient reaction kinetics, making it a versatile tool in organic synthesis. | ||||||
Tetravinylsilane | 1112-55-6 | sc-237082 | 5 g | $83.00 | ||
Tetravinylsilane is a versatile organosilicon compound characterized by its unique ability to undergo cross-coupling reactions, facilitating the formation of complex siloxane networks. Its multiple vinyl groups enhance reactivity, allowing for selective polymerization and functionalization. The compound exhibits interesting coordination chemistry, interacting with transition metals to form stable complexes. This behavior enables diverse synthetic routes and contributes to its role in advanced materials science. | ||||||
[3-(2-Aminoethylamino)propyl]trimethoxysilane | 1760-24-3 | sc-238452 | 100 ml | $63.00 | ||
[3-(2-Aminoethylamino)propyl]trimethoxysilane is a multifunctional organosilane that exhibits remarkable reactivity due to its amino and methoxy groups. It can engage in hydrolysis, leading to the formation of silanol species that promote siloxane bond formation. This compound also demonstrates unique ligand properties, facilitating metal coordination and enhancing catalytic pathways. Its ability to form stable silane networks underpins its significance in surface modification and adhesion applications. | ||||||
Vinylmagnesium bromide solution | 1826-67-1 | sc-301970 | 100 ml | $51.00 | ||
Vinylmagnesium bromide solution is a highly reactive organometallic compound characterized by its ability to participate in nucleophilic addition reactions. The presence of the vinyl group allows for unique interactions with electrophiles, facilitating the formation of carbon-carbon bonds. Its reactivity is influenced by the Grignard nature of the magnesium center, which enhances its role in various synthetic pathways. This compound also exhibits notable stability in solution, making it a versatile reagent in organic synthesis. |