Items 61 to 70 of 377 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Fosinoprilat Disodium Salt | 95399-71-6 | sc-207700 | 5 mg | $380.00 | ||
Fosinoprilat Disodium Salt is a phosphorus compound characterized by its unique phosphonate structure, which facilitates strong coordination with metal ions. This compound exhibits distinctive reactivity in hydrolysis reactions, leading to the formation of stable phosphonic acid derivatives. Its ionic nature enhances solubility in polar solvents, promoting efficient interactions in various chemical environments. The compound's ability to engage in specific electrostatic interactions further influences its reactivity and stability in diverse applications. | ||||||
SR 12813 | 126411-39-0 | sc-204296 sc-204296A | 10 mg 50 mg | $91.00 $345.00 | ||
SR 12813 is a phosphorus compound notable for its unique reactivity as an acid halide, which allows it to participate in acylation reactions with nucleophiles. Its structure promotes selective interactions with amines and alcohols, leading to the formation of stable esters and amides. The compound's electrophilic nature enhances its reactivity, making it a key player in synthetic pathways. Additionally, its ability to form transient intermediates can influence reaction kinetics, providing insights into mechanistic studies. | ||||||
(+)-1,2-Bis[(2S,5S)-2,5-dimethylphospholano]benzene | 136735-95-0 | sc-237667 | 100 mg | $68.00 | ||
(+)-1,2-Bis[(2S,5S)-2,5-dimethylphospholano]benzene is a phosphorus compound distinguished by its chiral phospholane framework, which facilitates unique stereochemical interactions. This compound exhibits remarkable selectivity in coordination with transition metals, enhancing catalytic activity in various reactions. Its dual phospholane groups contribute to a dynamic electronic environment, influencing reactivity patterns and enabling the formation of diverse organophosphorus derivatives. The compound's structural intricacies also allow for intriguing conformational flexibility, impacting its behavior in complexation and ligand exchange processes. | ||||||
4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene | 161265-03-8 | sc-238986 sc-238986A | 1 g 5 g | $62.00 $260.00 | ||
4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene is a phosphorus compound characterized by its unique xanthene backbone, which provides a rigid yet flexible structure. This compound exhibits strong chelating properties due to its diphenylphosphino groups, facilitating effective metal coordination. Its distinct electronic properties enhance reactivity in cross-coupling reactions, while the spatial arrangement of its ligands allows for selective interactions, influencing reaction pathways and kinetics in organometallic chemistry. | ||||||
Tris(2-ethylhexyl) phosphate | 78-42-2 | sc-251393 | 25 ml | $32.00 | 9 | |
Tris(2-ethylhexyl) phosphate is a phosphorus compound notable for its ability to act as a plasticizer and flame retardant. Its branched alkyl chains enhance solubility and compatibility with various polymers, promoting molecular mobility. The compound exhibits strong hydrogen bonding capabilities, influencing its interactions with polar solvents. Additionally, its unique steric configuration allows for effective dispersion in formulations, impacting thermal stability and mechanical properties of materials. | ||||||
Tris(2-butoxyethyl) phosphate | 78-51-3 | sc-237373 | 100 g | $52.00 | 10 | |
Tris(2-butoxyethyl) phosphate is a phosphorus compound characterized by its unique molecular structure, which facilitates strong dipole-dipole interactions. This compound exhibits excellent compatibility with a range of organic solvents, enhancing its utility in various formulations. Its ability to form stable complexes with metal ions can influence reaction kinetics, while its viscosity and surface tension properties contribute to its effectiveness in modifying the physical characteristics of mixtures. | ||||||
Dibutyl phosphate | 107-66-4 | sc-257325 | 250 ml | $52.00 | ||
Dibutyl phosphate is a phosphorus compound notable for its ability to form hydrogen bonds, which enhances its solubility in polar solvents. This compound exhibits unique reactivity patterns, particularly in esterification and transesterification reactions, where it can act as a nucleophile. Its low volatility and moderate viscosity make it an effective medium for facilitating molecular interactions, while its surface-active properties can influence the stability of emulsions and dispersions. | ||||||
Tris(2-chloroethyl) phosphate | 115-96-8 | sc-229621 | 25 g | $26.00 | 8 | |
Tris(2-chloroethyl) phosphate is a phosphorus compound characterized by its ability to engage in electrophilic substitution reactions due to the presence of chlorine atoms. This compound exhibits significant dipole moments, enhancing its interactions with polar molecules. Its high density and low vapor pressure contribute to its stability in various environments, while its capacity to form complexes with metal ions can influence catalytic processes. Additionally, it demonstrates unique thermal stability, making it resistant to degradation under heat. | ||||||
Triisopropyl phosphate | 513-02-0 | sc-229581 | 100 g | $40.00 | ||
Triisopropyl phosphate is a phosphorus compound notable for its role as a versatile solvent and plasticizer. Its branched isopropyl groups enhance solubility in organic solvents, facilitating interactions with various substrates. The compound exhibits strong hydrogen bonding capabilities, which can influence reaction kinetics and enhance the stability of formulations. Additionally, its low volatility and high flash point contribute to its safety in handling, while its ability to form stable complexes with metal ions can modify catalytic activity in chemical processes. | ||||||
Phenylphosphonic dichloride | 824-72-6 | sc-250705 | 100 ml | $59.00 | ||
Phenylphosphonic dichloride is a phosphorus compound characterized by its reactivity as an acid chloride, enabling it to participate in acylation reactions. Its electrophilic nature allows for efficient nucleophilic attack by amines and alcohols, leading to the formation of phosphonates and phosphonic esters. The presence of chlorine atoms enhances its ability to form stable intermediates, influencing reaction pathways and kinetics. Additionally, its aromatic structure contributes to unique π-π stacking interactions, which can affect solubility and reactivity in various chemical environments. | ||||||