Items 51 to 60 of 470 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Diethylenetriamine-pentaacetic acid calcium trisodium salt | 207226-35-5 | sc-227855 | 100 g | $218.00 | ||
Diethylenetriamine-pentaacetic acid calcium trisodium salt is a synthetic reagent characterized by its exceptional chelating ability, forming strong complexes with metal ions. Its multi-dentate structure enables effective binding, influencing solubility and stability in various environments. The compound exhibits unique reactivity patterns, facilitating ion exchange processes and enhancing selectivity in complexation reactions. Its distinct ionic properties contribute to its behavior in diverse chemical systems, impacting reaction dynamics and pathways. | ||||||
Tetrakis[N-phthaloyl-(R)-tert-leucinato]dirhodium Bis(ethyl Acetate) Adduct | 380375-05-3 | sc-296511 | 100 mg | $638.00 | ||
Tetrakis[N-phthaloyl-(R)-tert-leucinato]dirhodium Bis(ethyl Acetate) Adduct is a synthetic reagent notable for its unique coordination chemistry and ability to stabilize reactive intermediates. The compound exhibits distinct ligand interactions, promoting selective catalytic pathways. Its robust framework enhances reaction kinetics, allowing for efficient transformations in organometallic processes. Additionally, the adduct's solubility in ethyl acetate facilitates its application in diverse synthetic methodologies, influencing reactivity and product formation. | ||||||
Tetrakis[N-phthaloyl-(S)-tert-leucinato]dirhodium Bis(ethyl Acetate) Adduct | sc-296513 | 100 mg | $638.00 | |||
Tetrakis[N-phthaloyl-(S)-tert-leucinato]dirhodium Bis(ethyl Acetate) Adduct serves as a versatile synthetic reagent characterized by its intricate ligand architecture and ability to modulate electronic environments. This compound engages in unique metal-ligand interactions, which can fine-tune reaction selectivity and enhance catalytic efficiency. Its solvation properties in ethyl acetate further optimize reaction conditions, promoting diverse synthetic pathways and influencing mechanistic outcomes in various chemical transformations. | ||||||
Tetrabutylammonium tetrafluoroborate | 429-42-5 | sc-253658 sc-253658A | 5 g 25 g | $33.00 $90.00 | ||
Tetrabutylammonium tetrafluoroborate is a highly effective synthetic reagent known for its ionic nature and ability to stabilize charged intermediates. Its unique structure facilitates strong ion-pairing interactions, enhancing reaction rates and selectivity in various organic transformations. The compound's solubility in polar solvents allows for efficient phase transfer catalysis, while its low viscosity contributes to improved mass transfer during reactions, making it a valuable tool in synthetic chemistry. | ||||||
DCC | 538-75-0 | sc-239713 sc-239713A | 25 g 100 g | $71.00 $204.00 | 3 | |
Dicyclohexylcarbodiimide (DCC) is a prominent synthetic reagent recognized for its role in facilitating amide bond formation through its unique reactivity as a coupling agent. It promotes the activation of carboxylic acids, enabling efficient nucleophilic attack by amines. DCC's ability to form stable intermediates enhances reaction kinetics, while its hydrophobic nature aids in driving reactions to completion by minimizing side reactions in aqueous environments. | ||||||
Rubidium acetate | 563-67-7 | sc-281144 sc-281144A | 25 g 100 g | $157.00 $754.00 | ||
Rubidium acetate serves as a versatile synthetic reagent, notable for its role in facilitating various organic transformations. Its unique ionic character allows for effective solvation of polar substrates, enhancing reaction rates. The compound can participate in transesterification and acylation reactions, where it acts as a source of acetate ions. Additionally, its ability to stabilize charged intermediates contributes to improved selectivity and yields in complex synthetic pathways. | ||||||
4-Methylmorpholine N-oxide | 7529-22-8 | sc-252180 sc-252180A | 5 g 25 g | $33.00 $114.00 | ||
4-Methylmorpholine N-oxide is a distinctive synthetic reagent known for its role as an oxidizing agent in organic synthesis. Its unique structure allows for strong hydrogen bonding interactions, enhancing solubility in polar solvents. This compound can effectively activate substrates for oxidation reactions, promoting the formation of various functional groups. Its ability to stabilize transition states leads to increased reaction efficiency and selectivity in complex synthetic routes. | ||||||
Ammonium sodium phosphate dibasic tetrahydrate | 7783-13-3 | sc-239241 sc-239241A | 100 g 500 g | $41.00 $82.00 | ||
Ammonium sodium phosphate dibasic tetrahydrate serves as a versatile synthetic reagent, notable for its ability to act as a buffering agent in various chemical reactions. Its unique crystalline structure facilitates ionic interactions, enhancing solubility in aqueous environments. This compound can influence reaction kinetics by modulating pH levels, thereby affecting the stability of intermediates. Additionally, its hygroscopic nature allows it to maintain moisture, which can be crucial in certain synthetic pathways. | ||||||
N,N′-Bis(salicylidene)ethylenediamine Iron(II) | 14167-12-5 | sc-295818 sc-295818A | 1 g 5 g | $376.00 $1107.00 | ||
N,N'-Bis(salicylidene)ethylenediamine Iron(II) is a distinctive synthetic reagent characterized by its chelating properties, forming stable complexes with metal ions. Its bidentate ligand structure promotes specific molecular interactions, enhancing selectivity in coordination chemistry. The compound exhibits unique redox behavior, facilitating electron transfer processes. Additionally, its planar geometry contributes to effective π-π stacking interactions, influencing reaction pathways and kinetics in various synthetic applications. | ||||||
Ammonium phosphomolybdate hydrate | 54723-94-3 | sc-239240 | 50 g | $115.00 | ||
Ammonium phosphomolybdate hydrate is a versatile synthetic reagent known for its ability to form polyoxometalate structures, which exhibit unique catalytic properties. Its rich network of hydrogen bonding enhances solubility and stability in various solvents, facilitating diverse reaction environments. The compound's ability to act as a Lewis acid allows it to engage in electrophilic interactions, influencing reaction kinetics and selectivity in organic synthesis. Its distinct crystalline form also contributes to its reactivity and interaction with other chemical species. |