Items 81 to 90 of 470 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Decaborane(14) | 17702-41-9 | sc-255069A sc-255069 sc-255069B | 1 g 5 g 25 g | $155.00 $500.00 $1600.00 | ||
Decaborane(14) serves as a versatile synthetic reagent, characterized by its unique boron-hydrogen framework that enables strong interactions with electron-rich substrates. Its ability to form stable complexes with various nucleophiles allows for selective boron transfer reactions. The compound exhibits distinctive reactivity, often engaging in unique pathways that facilitate the formation of boron-containing intermediates, thereby expanding the toolkit for synthetic organic chemists. | ||||||
Tris(hexafluoroacetylacetonato)iron(III) | 17786-67-3 | sc-296663 | 1 g | $364.00 | ||
Tris(hexafluoroacetylacetonato)iron(III) is a notable synthetic reagent distinguished by its ability to form robust chelate complexes with metal ions, enhancing reaction specificity. Its hexafluoroacetylacetonate ligands exhibit strong electron-withdrawing properties, influencing reaction kinetics and promoting unique pathways in coordination chemistry. This compound's distinctive solubility profile and thermal stability further facilitate its use in various synthetic transformations, making it a valuable tool in advanced materials synthesis. | ||||||
Bis[tetrakis(hydroxymethyl)phosphonium] sulfate solution | 55566-30-8 | sc-234091 | 250 ml | $58.00 | ||
Bis[tetrakis(hydroxymethyl)phosphonium] sulfate solution serves as a versatile synthetic reagent, characterized by its ability to engage in unique molecular interactions through its phosphonium groups. These groups facilitate the formation of stable intermediates, enhancing reaction rates and selectivity in various synthetic pathways. The solution's high solubility in polar solvents and its capacity to act as a strong reducing agent contribute to its effectiveness in diverse chemical transformations, making it a significant player in synthetic chemistry. | ||||||
Acetaldehyde ammonia trimer | 58052-80-5 | sc-257047 | 100 g | $89.00 | ||
Acetaldehyde ammonia trimer is a notable synthetic reagent distinguished by its ability to form hydrogen bonds and engage in nucleophilic reactions. Its unique trimeric structure allows for enhanced stability and reactivity, facilitating the formation of complex intermediates. This compound exhibits distinct kinetic properties, promoting rapid reaction rates in condensation and polymerization processes. Its solubility in various solvents further broadens its applicability in synthetic methodologies. | ||||||
Benzalkonium chloride | 63449-41-2 | sc-257126 | 100 g | $79.00 | ||
Benzalkonium chloride is a versatile synthetic reagent characterized by its amphiphilic nature, enabling it to interact effectively with both polar and nonpolar environments. Its quaternary ammonium structure facilitates strong electrostatic interactions, enhancing its ability to stabilize charged intermediates. This compound exhibits unique micelle formation properties, influencing reaction pathways and kinetics in various synthetic processes. Its surfactant-like behavior also contributes to its role in modifying interfacial tension in reactions. | ||||||
Calix[8]arene | 82452-93-5 | sc-234273 | 1 g | $106.00 | ||
Calix[8]arene is a unique synthetic reagent known for its ability to form host-guest complexes through selective molecular recognition. Its cup-shaped structure allows for the encapsulation of cations and small molecules, enhancing reaction specificity. The compound exhibits dynamic conformational flexibility, which can influence reaction kinetics and pathways. Additionally, its ability to engage in hydrogen bonding and π-π stacking interactions contributes to its effectiveness in catalyzing various synthetic transformations. | ||||||
Tri-tert-butyl 1,4,7,10-tetraazacyclododecane-1,4,7-triacetate | 122555-91-3 | sc-237238 | 250 mg | $231.00 | ||
Tri-tert-butyl 1,4,7,10-tetraazacyclododecane-1,4,7-triacetate is a versatile synthetic reagent characterized by its robust chelating properties. The tetraazacyclododecane framework facilitates strong coordination with metal ions, enhancing catalytic activity in various reactions. Its sterically hindered tert-butyl groups provide stability and prevent aggregation, while the acetate moieties enable selective interactions with electrophiles. This compound's unique structure promotes efficient reaction pathways and enhances selectivity in complex synthetic environments. | ||||||
Chlorotripyrrolidinophosphonium hexafluorophosphate | 133894-48-1 | sc-252597 | 5 g | $110.00 | ||
Chlorotripyrrolidinophosphonium hexafluorophosphate is a potent synthetic reagent known for its unique phosphonium cation, which enhances nucleophilicity in various reactions. The presence of hexafluorophosphate anions contributes to its high ionic strength, facilitating rapid ion exchange processes. This compound exhibits remarkable stability under diverse conditions, allowing for efficient activation of substrates. Its distinctive molecular interactions enable streamlined pathways in complex organic transformations, making it a valuable tool in synthetic chemistry. | ||||||
Fluoro-N,N,N′,N′-bis(tetramethylene)formamidinium hexafluorophosphate | 164298-25-3 | sc-250001 | 5 g | $148.00 | ||
Fluoro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate serves as a versatile synthetic reagent characterized by its unique dual cationic structure, which promotes enhanced electrophilicity. The hexafluorophosphate anion imparts significant solubility in polar solvents, facilitating swift reaction kinetics. Its ability to stabilize reactive intermediates allows for efficient transformations, while specific molecular interactions enable selective pathways in complex synthetic sequences, making it an essential component in advanced organic synthesis. | ||||||
2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane | 175845-21-3 | sc-251884 | 1 g | $146.00 | ||
2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane is a distinctive synthetic reagent known for its unique bicyclic structure, which enhances steric hindrance and influences reactivity. Its nitrogen-rich framework facilitates strong coordination with metal catalysts, promoting efficient electron transfer. This compound exhibits remarkable stability under various conditions, allowing for controlled reaction pathways and the formation of complex molecular architectures in synthetic chemistry. |