Items 41 to 50 of 468 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tetrakis(dimethylamino)ethylene | 996-70-3 | sc-253676 sc-253676A sc-253676B | 1 g 10 g 50 g | $109.00 $520.00 $2081.00 | ||
Tetrakis(dimethylamino)ethylene is a versatile synthetic reagent known for its unique electron-rich structure, which enhances its nucleophilicity. This compound exhibits remarkable stability under various conditions, allowing it to participate in diverse reaction pathways, including cycloadditions and polymerizations. Its ability to stabilize radical intermediates contributes to its effectiveness in facilitating complex transformations, making it a significant player in synthetic methodologies. | ||||||
Strontium peroxide | 1314-18-7 | sc-229334 | 100 g | $42.00 | ||
Strontium peroxide serves as a potent synthetic reagent characterized by its strong oxidizing properties. It readily decomposes to release oxygen, facilitating oxidation reactions in various organic substrates. The compound's ability to generate reactive oxygen species enhances its role in promoting radical reactions and initiating polymerization processes. Additionally, its solid-state structure allows for unique interactions with other reagents, influencing reaction kinetics and pathways in synthetic applications. | ||||||
2-(2-Hydroxy-5-methylphenyl)benzotriazole | 2440-22-4 | sc-225040 | 25 g | $65.00 | ||
2-(2-Hydroxy-5-methylphenyl)benzotriazole is a versatile synthetic reagent known for its exceptional UV-absorbing properties, which stem from its unique molecular structure. This compound exhibits strong π-π stacking interactions, enhancing its stability and reactivity in various chemical environments. Its ability to form hydrogen bonds facilitates selective reactions, while its distinct electronic properties allow for efficient energy transfer in photochemical processes, making it a valuable tool in synthetic chemistry. | ||||||
Brucine Hydrochloride Monohydrate | 5786-96-9 | sc-293962 | 5 g | $120.00 | ||
Brucine Hydrochloride Monohydrate is a notable synthetic reagent characterized by its chiral nature, which enables it to participate in asymmetric synthesis. Its unique molecular interactions, particularly through hydrogen bonding and steric effects, influence reaction pathways and kinetics. The compound's solubility in polar solvents enhances its reactivity, allowing for efficient participation in nucleophilic substitutions and other transformations, making it a significant player in organic synthesis. | ||||||
Aluminum chloride anhydrous | 7446-70-0 | sc-214528 sc-214528B sc-214528A | 250 g 500 g 1 kg | $94.00 $99.00 $136.00 | ||
Aluminum chloride anhydrous is a versatile synthetic reagent known for its Lewis acid properties, facilitating electrophilic aromatic substitutions and Friedel-Crafts reactions. Its ability to form complexes with various substrates enhances reaction rates and selectivity. The compound's hygroscopic nature allows it to readily absorb moisture, influencing its reactivity in anhydrous conditions. Additionally, its high surface area promotes catalytic activity, making it essential in various synthetic pathways. | ||||||
Magnesium bromide | 7789-48-2 | sc-250274 sc-250274A | 10 g 50 g | $39.00 $116.00 | ||
Magnesium bromide serves as a potent synthetic reagent, exhibiting unique coordination chemistry that enables it to act as a Lewis acid in various reactions. Its ability to form stable complexes with organic substrates enhances reaction efficiency and selectivity. The compound's ionic nature contributes to its solubility in polar solvents, facilitating diverse reaction pathways. Furthermore, its role in facilitating nucleophilic substitutions and coupling reactions underscores its significance in synthetic organic chemistry. | ||||||
Calcium phosphate monobasic monohydrate | 10031-30-8 | sc-223856 sc-223856A | 100 g 500 g | $57.00 $99.00 | ||
Calcium phosphate monobasic monohydrate is a versatile synthetic reagent known for its role in facilitating precipitation reactions and ion exchange processes. Its unique ability to interact with various cations and anions allows for the formation of stable complexes, enhancing reaction kinetics. The compound's hygroscopic nature aids in maintaining moisture levels in reactions, while its crystalline structure contributes to its solubility in aqueous environments, promoting effective synthesis pathways. | ||||||
Sodium phosphite dibasic pentahydrate | 13517-23-2 | sc-229314 | 250 g | $51.00 | ||
Sodium phosphite dibasic pentahydrate serves as a crucial synthetic reagent, notable for its capacity to act as a reducing agent in various chemical transformations. Its dual basicity enables it to engage in complexation with metal ions, influencing reaction pathways and enhancing selectivity. The compound's high solubility in water facilitates rapid dissolution, promoting efficient mass transfer during reactions. Additionally, its stability under diverse conditions makes it a reliable choice for synthetic applications. | ||||||
Nitrosyl tetrafluoroborate | 14635-75-7 | sc-250572 sc-250572A | 5 g 25 g | $64.00 $250.00 | ||
Nitrosyl tetrafluoroborate is a distinctive synthetic reagent characterized by its ability to facilitate unique molecular interactions through the release of nitrosyl groups. This compound exhibits strong electrophilic properties, allowing it to engage in selective reactions with nucleophiles. Its high reactivity and stability under specific conditions enable it to serve as a versatile intermediate in various synthetic pathways, influencing reaction kinetics and product formation. The compound's unique coordination chemistry further enhances its utility in complex synthesis. | ||||||
1,3,4,6-Tetrachloro-3α,6α-diphenylglycouril | 51592-06-4 | sc-251587 | 250 mg | $228.00 | ||
1,3,4,6-Tetrachloro-3α,6α-diphenylglycouril is a synthetic reagent notable for its ability to form stable complexes with various metal ions, enhancing its role in coordination chemistry. Its unique structure allows for selective interactions with nucleophiles, promoting specific reaction pathways. The compound's robust chlorinated framework contributes to its reactivity, facilitating diverse synthetic transformations while influencing the kinetics of reactions through steric and electronic effects. | ||||||