Items 431 to 440 of 470 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Sulfur trioxide trimethylamine complex | 3162-58-1 | sc-229350 sc-229350A | 5 g 100 g | $33.00 $107.00 | ||
Sulfur trioxide trimethylamine complex acts as a highly effective synthetic reagent, characterized by its strong electrophilic nature. The interaction between sulfur trioxide and trimethylamine creates a stable adduct that enhances nucleophilic attack in acylation reactions. This complex exhibits unique reactivity patterns, facilitating the formation of sulfonic acid derivatives. Its ability to engage in rapid reaction kinetics makes it a valuable tool for generating diverse functional groups in organic synthesis. | ||||||
Triethyloxonium hexachloroantimonate | 3264-67-3 | sc-229574 | 5 g | $73.00 | ||
Triethyloxonium hexachloroantimonate serves as a potent synthetic reagent, notable for its ability to generate highly reactive ethyl cation intermediates. This compound exhibits exceptional electrophilicity, enabling it to facilitate alkylation and acylation reactions with remarkable efficiency. Its unique interactions with nucleophiles lead to the formation of various ether and ester derivatives, while its stability under specific conditions allows for controlled reaction pathways, enhancing synthetic versatility in complex organic transformations. | ||||||
Didodecyldimethylammonium bromide | 3282-73-3 | sc-239715 sc-239715A | 2 g 10 g | $82.00 $255.00 | 1 | |
Didodecyldimethylammonium bromide is a versatile synthetic reagent characterized by its amphiphilic nature, which promotes unique interactions with both polar and nonpolar substrates. This compound exhibits significant surface activity, facilitating micelle formation and enhancing solubilization processes. Its quaternary ammonium structure allows for effective ion-pairing and stabilization of reactive intermediates, making it a valuable tool in various synthetic pathways and reaction mechanisms. | ||||||
Cesium formate | 3495-36-1 | sc-239490 | 25 g | $57.00 | ||
Cesium formate serves as a distinctive synthetic reagent, notable for its high ionic strength and ability to stabilize charged species in solution. Its unique properties enable it to act as a powerful polar solvent, enhancing reaction kinetics in various organic transformations. The compound's ability to form strong hydrogen bonds facilitates specific molecular interactions, promoting selectivity in reactions and improving yields. Additionally, its low viscosity aids in efficient mixing and heat transfer during synthesis. | ||||||
Tetrabutylammonium thiocyanate | 3674-54-2 | sc-251162 | 10 g | $62.00 | ||
Tetrabutylammonium thiocyanate is a versatile synthetic reagent characterized by its ability to solubilize a wide range of organic and inorganic compounds. Its quaternary ammonium structure enhances ion-pairing interactions, facilitating nucleophilic substitutions and other reaction pathways. The compound's unique ability to stabilize thiocyanate ions allows for selective reactions, while its low volatility and high solubility contribute to efficient reaction conditions and improved product yields. | ||||||
Triphenylphosphine Selenide | 3878-44-2 | sc-296644 | 5 g | $107.00 | ||
Triphenylphosphine selenide serves as a potent synthetic reagent, notable for its role in facilitating phosphine-mediated transformations. Its unique selenium atom enhances nucleophilicity, enabling efficient electrophilic attacks in various organic reactions. The compound exhibits strong coordination properties, allowing it to form stable complexes with metals, which can influence reaction kinetics and selectivity. Additionally, its distinct electronic properties contribute to its effectiveness in promoting diverse synthetic pathways. | ||||||
Triphenylphosphine sulfide | 3878-45-3 | sc-251384 | 5 g | $33.00 | ||
Triphenylphosphine sulfide is a versatile synthetic reagent, recognized for its ability to engage in nucleophilic substitution reactions. The sulfur atom in its structure imparts unique reactivity, allowing it to participate in the formation of thiophosphonium salts. This compound also demonstrates significant electron-donating capabilities, enhancing its interactions with electrophiles. Its stability and solubility in organic solvents further facilitate a range of synthetic applications, making it a valuable tool in organic chemistry. | ||||||
Trihexylphosphine | 4168-73-4 | sc-296621 | 25 ml | $444.00 | ||
Trihexylphosphine is a notable synthetic reagent characterized by its strong nucleophilic properties, which enable it to effectively coordinate with various metal centers. Its long hydrocarbon chains enhance solubility in nonpolar solvents, promoting efficient reaction kinetics in organometallic chemistry. This compound can facilitate the formation of phosphine oxides and phosphonium salts, showcasing its versatility in diverse synthetic pathways. Its unique steric and electronic properties make it an essential component in complex organic transformations. | ||||||
Trimethylphenylammonium tribromide | 4207-56-1 | sc-253766 | 25 g | $79.00 | ||
Trimethylphenylammonium tribromide serves as a versatile synthetic reagent, notable for its ability to act as a brominating agent in organic synthesis. Its quaternary ammonium structure enhances solubility in polar solvents, facilitating rapid ionic interactions. The compound exhibits distinct reactivity patterns, enabling selective bromination of aromatic compounds and alkenes. Its unique electronic configuration allows for efficient electron transfer, making it a valuable tool in various synthetic methodologies. | ||||||
1-Benzoyl-1H-benzotriazole | 4231-62-3 | sc-224532 | 1 g | $88.00 | ||
1-Benzoyl-1H-benzotriazole is a synthetic reagent recognized for its role as a UV-absorbing agent in polymer chemistry. Its unique structure allows for strong π-π stacking interactions, enhancing stability in photostabilization applications. The compound exhibits notable reactivity with electrophiles, facilitating the formation of stable adducts. Additionally, its ability to undergo intramolecular hydrogen bonding contributes to its effectiveness in controlling reaction pathways and kinetics in complex organic transformations. |