Items 281 to 290 of 468 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tetraoctadecyl Orthotitanate | 5128-29-0 | sc-296520 sc-296520A | 25 g 500 g | $84.00 $599.00 | ||
Tetraoctadecyl Orthotitanate is a notable synthetic reagent characterized by its ability to form stable complexes with various ligands, enhancing its reactivity in coordination chemistry. Its long hydrocarbon chains contribute to unique solubility properties, allowing for selective interactions in non-polar environments. This compound exhibits distinct pathways in polymerization processes, where it acts as a catalyst, influencing reaction rates and product distribution through its metal-centered coordination dynamics. | ||||||
Ethylenediamine-N,N′-diacetic acid | 5657-17-0 | sc-239968 | 1 g | $71.00 | ||
Ethylenediamine-N,N'-diacetic acid is a versatile synthetic reagent known for its chelating properties, effectively binding metal ions through multiple coordination sites. This compound facilitates intricate reaction pathways, enhancing selectivity in complexation reactions. Its unique ability to stabilize transition states can significantly influence reaction kinetics, making it a valuable tool in various synthetic applications. Additionally, its solubility in polar solvents allows for efficient interaction with a range of substrates. | ||||||
3-Phenyl-2,4-pentanedione | 5910-25-8 | sc-289229 sc-289229A | 1 g 5 g | $242.00 $785.00 | ||
3-Phenyl-2,4-pentanedione serves as a notable synthetic reagent, characterized by its ability to participate in enolization and tautomerization, leading to diverse reactivity patterns. Its diketone structure enables strong hydrogen bonding and π-π stacking interactions, which can stabilize reactive intermediates. This compound also exhibits unique electrophilic properties, facilitating Michael additions and condensation reactions, thus expanding its utility in synthetic organic chemistry. | ||||||
1,1′-Thiocarbonyldiimidazole | 6160-65-2 | sc-255887 | 5 g | $123.00 | ||
1,1'-Thiocarbonyldiimidazole is a versatile synthetic reagent known for its unique ability to activate nucleophiles through thiocarbonyl group interactions. This compound promotes the formation of thiourea derivatives via efficient nucleophilic substitution pathways. Its distinct reactivity allows for the generation of stable intermediates, enhancing reaction kinetics in various coupling reactions. Additionally, its polar nature aids in solvation, influencing reaction dynamics in organic synthesis. | ||||||
Strontium | 7440-24-6 | sc-253606 | 5 g | $53.00 | ||
Strontium serves as a potent synthetic reagent, particularly in the formation of organometallic compounds. Its ability to engage in electron transfer processes facilitates the generation of reactive intermediates, which can enhance reaction rates in cross-coupling reactions. Strontium's metallic character contributes to its unique interactions with ligands, promoting the formation of stable complexes. This reactivity is further influenced by its propensity to stabilize anions, making it a valuable tool in synthetic organic chemistry. | ||||||
Barium | 7440-39-3 | sc-252400 | 10 g | $63.00 | ||
Barium acts as a versatile synthetic reagent, particularly in the synthesis of various organometallic compounds. Its high reactivity allows it to readily form barium salts, which can participate in nucleophilic substitution reactions. The metal's ability to stabilize certain anions enhances its role in facilitating complexation reactions. Additionally, barium's unique electron configuration contributes to its effectiveness in catalyzing diverse chemical transformations, making it a key player in synthetic pathways. | ||||||
Lithium hydride | 7580-67-8 | sc-250259 sc-250259A | 5 g 10 g | $51.00 $92.00 | ||
Lithium hydride serves as a potent synthetic reagent, particularly noted for its strong reducing properties. It readily donates hydride ions, facilitating reductions in organic synthesis. Its high ionic character promotes rapid reaction kinetics, enabling swift interactions with electrophiles. The compound's ability to form stable complexes with various substrates enhances its utility in generating lithium-based intermediates, making it essential for diverse synthetic routes and transformations. | ||||||
Titanium(II) hydride | 7704-98-5 | sc-251252 | 100 g | $107.00 | ||
Titanium(II) hydride is a versatile synthetic reagent characterized by its unique ability to engage in metal-hydride transfer reactions. Its low oxidation state allows for effective coordination with various ligands, promoting the formation of titanium complexes that can catalyze a range of organic transformations. The compound exhibits notable stability under inert conditions, facilitating controlled reactions and enabling selective reductions, which are crucial in synthetic organic chemistry. | ||||||
Barium sulfate | 7727-43-7 | sc-239277 sc-239277A | 1 kg 5 kg | $224.00 $326.00 | ||
Barium sulfate serves as a unique synthetic reagent, notable for its high density and low solubility in water, which influences its behavior in various chemical environments. Its ability to act as a sulfate source allows for specific ionic interactions, facilitating precipitation reactions. The compound's inert nature under a wide range of conditions makes it an excellent choice for applications requiring stability, while its crystalline structure contributes to distinct scattering properties in analytical techniques. | ||||||
Nitrosylsulfuric acid solution | 7782-78-7 | sc-236182 | 250 ml | $122.00 | ||
Nitrosylsulfuric acid solution is a distinctive synthetic reagent characterized by its ability to engage in electrophilic aromatic substitution reactions, making it effective in introducing nitro and sulfonyl groups into organic compounds. Its unique molecular interactions enable the formation of stable intermediates, enhancing reaction kinetics. The solution's strong oxidizing properties facilitate the transformation of various substrates, while its viscosity and density influence mixing and reaction dynamics in synthetic pathways. | ||||||