Items 321 to 330 of 377 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Vinylphosphonic acid | 1746-03-8 | sc-237411 | 250 g | $739.00 | ||
Vinylphosphonic acid is a phosphorus compound notable for its vinyl group, which facilitates unique polymerization reactions and enhances its reactivity in various chemical processes. The presence of the phosphonic acid moiety allows for strong hydrogen bonding and ionic interactions, promoting its role in forming stable complexes with metal ions. Additionally, its ability to participate in Michael additions and other nucleophilic reactions underscores its versatility in organic synthesis and materials science. | ||||||
Phenylphosphinic acid | 1779-48-2 | sc-236377 sc-236377A | 5 g 100 g | $22.00 $30.00 | ||
Phenylphosphinic acid is a phosphorus compound characterized by its phenyl group, which influences its electronic properties and steric effects. This structure enhances its ability to engage in electrophilic aromatic substitution reactions, making it a key player in various synthetic pathways. The acid exhibits strong acidity due to the presence of the phosphinic group, facilitating proton transfer and enabling it to act as a catalyst in diverse chemical transformations. Its unique interactions with nucleophiles further expand its reactivity profile. | ||||||
Dibutyl phosphite | 1809-19-4 | sc-252686 | 100 ml | $31.00 | ||
Dibutyl phosphite is a phosphorus compound notable for its role as a versatile ligand in coordination chemistry. Its alkyl groups enhance solubility and steric hindrance, influencing its reactivity with metal ions. The compound participates in nucleophilic substitution reactions, where the phosphite moiety can act as a nucleophile, facilitating the formation of phosphonate esters. Additionally, its ability to stabilize reactive intermediates makes it significant in various organic synthesis pathways. | ||||||
Chloromethylphosphonic acid dichloride | 1983-26-2 | sc-234339 | 10 g | $80.00 | ||
Chloromethylphosphonic acid dichloride is a phosphorus compound characterized by its reactivity as an acid halide, particularly in acylation reactions. The presence of chloromethyl and dichloride groups enhances its electrophilic nature, allowing it to readily engage in nucleophilic attack. This compound exhibits unique behavior in forming stable intermediates, which can lead to diverse phosphorus-containing derivatives. Its distinct molecular interactions facilitate the synthesis of complex organophosphorus compounds, showcasing its utility in various chemical transformations. | ||||||
2-Aminoethylphosphonic acid | 2041-14-7 | sc-225161 | 250 mg | $86.00 | ||
2-Aminoethylphosphonic acid is a phosphorus compound notable for its dual functionality as both an amine and a phosphonic acid. This unique structure allows it to participate in hydrogen bonding and chelation, influencing its reactivity in condensation and substitution reactions. The presence of the amino group enhances its nucleophilicity, enabling it to form stable complexes with metal ions. Its distinct molecular interactions contribute to its role in various biochemical pathways, showcasing its versatility in synthetic chemistry. | ||||||
Bis(diphenylphosphino)methane | 2071-20-7 | sc-252460 | 5 g | $37.00 | ||
Bis(diphenylphosphino)methane is a phosphorus compound characterized by its bidentate ligand properties, enabling it to form stable chelates with transition metals. The sterically bulky diphenylphosphino groups enhance its ability to stabilize low oxidation states, facilitating unique catalytic pathways in cross-coupling reactions. Its robust electron-donating ability and distinctive steric profile contribute to its effectiveness in promoting reaction kinetics, making it a key player in organometallic chemistry. | ||||||
4-(Diphenylphosphino)benzoic acid | 2129-31-9 | sc-226411 | 1 g | $80.00 | ||
4-(Diphenylphosphino)benzoic acid is a phosphorus compound notable for its ability to act as a versatile ligand in coordination chemistry. The presence of the diphenylphosphino group allows for strong π-π stacking interactions and hydrogen bonding, enhancing its reactivity in various catalytic processes. Its unique structural features facilitate the formation of stable complexes with metals, influencing reaction mechanisms and selectivity in organometallic transformations. | ||||||
Methyldiphenylphosphine oxide | 2129-89-7 | sc-228590 | 5 g | $51.00 | ||
Methyldiphenylphosphine oxide is a phosphorus compound characterized by its strong electron-donating properties, which enhance its role in various chemical reactions. The presence of the phosphine oxide functional group allows for significant dipole interactions, promoting solubility in polar solvents. Its unique steric and electronic properties facilitate selective coordination with transition metals, influencing reaction pathways and kinetics in organometallic chemistry. This compound also exhibits notable stability under various conditions, making it a key player in synthetic applications. | ||||||
Diphenylvinylphosphine | 2155-96-6 | sc-227926 | 5 g | $110.00 | ||
Diphenylvinylphosphine is a phosphorus compound distinguished by its unique vinyl group, which introduces reactivity through conjugation and enhances its ability to participate in various coupling reactions. The compound exhibits significant π-π stacking interactions due to its aromatic rings, influencing its behavior in complexation and catalysis. Its sterically hindered structure allows for selective reactivity, making it a versatile intermediate in organic synthesis and materials science. | ||||||
1-Naphthyl phosphate, disodium salt | 2183-17-7 | sc-206185 sc-206185A | 100 mg 1 g | $52.00 $113.00 | ||
1-Naphthyl phosphate, disodium salt, is a phosphorus compound characterized by its naphthalene moiety, which facilitates strong π-π interactions and enhances solubility in polar solvents. This compound exhibits unique reactivity patterns, particularly in nucleophilic substitution reactions, due to the presence of the phosphate group. Its ionic nature contributes to its stability in aqueous environments, allowing for efficient ion exchange processes and influencing its behavior in various chemical pathways. | ||||||