Items 201 to 210 of 377 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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1,1′-Bis(di-tert-butylphosphino)ferrocene | 84680-95-5 | sc-224876 | 250 mg | $31.00 | ||
1,1'-Bis(di-tert-butylphosphino)ferrocene is a phosphorus compound characterized by its unique bimetallic structure, which facilitates strong metal-ligand interactions. The bulky di-tert-butylphosphino groups impart significant steric hindrance, influencing its coordination chemistry and reactivity. This compound exhibits remarkable stability and selectivity in catalytic processes, with its ferrocene core enhancing electron transfer capabilities, making it a key player in organometallic chemistry. | ||||||
N,N-Diisopropylmethylphosphonamidic chloride | 86030-43-5 | sc-253138 | 1 g | $74.00 | ||
N,N-Diisopropylmethylphosphonamidic chloride is a phosphorus compound notable for its reactivity as an acid halide. It features a phosphonamidic structure that allows for unique nucleophilic attack pathways, facilitating the formation of various derivatives. The presence of isopropyl groups enhances steric effects, influencing reaction kinetics and selectivity. This compound's ability to engage in diverse molecular interactions makes it a versatile building block in synthetic chemistry. | ||||||
(±)-Z-α-Phosphonoglycine trimethyl ester | 88568-95-0 | sc-255722 | 5 g | $199.00 | ||
(±)-Z-α-Phosphonoglycine trimethyl ester is a phosphorus compound characterized by its unique phosphonate structure, which enables specific interactions with nucleophiles. Its trimethyl ester groups enhance solubility and reactivity, allowing for efficient esterification and hydrolysis reactions. The compound exhibits distinct stereochemical properties that can influence reaction pathways, making it a valuable intermediate in various synthetic processes. Its behavior as a phosphorus compound is marked by its ability to participate in diverse chemical transformations. | ||||||
[1,1′-Bis(diphenylphosphino)ferrocene]palladium(II) Dichloride Dichloromethane Adduct | 95464-05-4 | sc-287201 sc-287201A | 1 g 5 g | $88.00 $287.00 | ||
[1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) dichloride dichloromethane adduct is a notable phosphorus compound distinguished by its bimetallic structure, which facilitates unique coordination chemistry. The ferrocene moiety enhances electron donation, promoting catalytic activity in cross-coupling reactions. Its dichloromethane adduct formation influences solubility and stability, while the phosphine ligands provide steric and electronic effects that modulate reaction kinetics and selectivity in various organometallic transformations. | ||||||
Naphthol AS-MX phosphate disodium salt | 96189-12-7 | sc-215539 sc-215539A sc-215539B | 100 mg 500 mg 1 g | $57.00 $130.00 $217.00 | 1 | |
Naphthol AS-MX phosphate disodium salt is a distinctive phosphorus compound characterized by its ability to form strong hydrogen bonds and engage in complexation with metal ions. This compound exhibits unique solubility properties in various solvents, enhancing its reactivity in nucleophilic substitution reactions. Its phosphate group contributes to significant electron delocalization, influencing reaction pathways and kinetics, while its structural features allow for versatile interactions in diverse chemical environments. | ||||||
(R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl | 99646-28-3 | sc-250868 | 250 mg | $44.00 | ||
(R)-(+)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl is a chiral phosphorus compound notable for its ability to facilitate asymmetric catalysis through its unique bidentate ligand structure. The sterically demanding di-p-tolylphosphino groups enhance selectivity in metal coordination, promoting distinct reaction pathways. Its rigid binaphthyl backbone contributes to pronounced stereoelectronic effects, influencing reactivity and enabling efficient chiral induction in various catalytic processes. | ||||||
Bis(4-trifluoromethylphenyl)phosphine | 99665-68-6 | sc-227376 | 250 mg | $200.00 | ||
Bis(4-trifluoromethylphenyl)phosphine is a phosphorus compound characterized by its strong electron-withdrawing trifluoromethyl groups, which significantly enhance its reactivity. This compound exhibits unique molecular interactions, particularly in coordination chemistry, where it can stabilize metal complexes through robust σ-donation and π-acceptance. Its distinctive electronic properties facilitate rapid reaction kinetics, making it a key player in various organophosphorus transformations and catalytic cycles. | ||||||
D-myo-Inositol-1,4,5-trisphosphate hexapotassium salt | 103476-24-0 | sc-201521 | 1 mg | $302.00 | 12 | |
D-myo-Inositol-1,4,5-trisphosphate hexapotassium salt is a phosphorus compound notable for its role in cellular signaling pathways. It acts as a secondary messenger, engaging in specific interactions with protein kinases and phosphatases, thereby influencing intracellular calcium levels. The compound's unique structure allows for effective binding to target proteins, facilitating rapid signal transduction. Its solubility in aqueous environments enhances its bioavailability, promoting dynamic cellular responses. | ||||||
Manganese(III) phosphate | 104663-56-1 | sc-269386 | 10 g | $70.00 | ||
Manganese(III) phosphate is a phosphorus compound characterized by its unique redox properties and ability to form stable complexes with various ligands. Its distinct oxidation state allows for versatile interactions in catalytic processes, particularly in oxidation reactions. The compound exhibits interesting thermal stability and can participate in electron transfer mechanisms, influencing reaction kinetics. Additionally, its crystalline structure contributes to its reactivity and solubility in specific solvents, enhancing its role in various chemical environments. | ||||||
Pamidronate, Disodium Salt | 109552-15-0 | sc-203178 | 10 mg | $76.00 | ||
Pamidronate, Disodium Salt is a phosphorus compound notable for its ability to chelate metal ions, forming stable complexes that influence various chemical equilibria. Its unique structure allows for selective interactions with calcium and magnesium, affecting mineralization processes. The compound exhibits significant solubility in aqueous environments, facilitating its participation in ion exchange reactions. Additionally, its anionic nature contributes to its reactivity in complexation and precipitation reactions, enhancing its versatility in diverse chemical systems. |