Items 91 to 100 of 377 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Uridine-5′-triphosphate trisodium salt dihydrate | 116295-90-0 | sc-286856 sc-286856A | 1 g 5 g | $62.00 $228.00 | 1 | |
Uridine-5'-triphosphate trisodium salt dihydrate is a phosphorus compound characterized by its triphosphate structure, which facilitates high-energy phosphate transfer. This compound exhibits unique interactions with enzymes, enhancing catalytic efficiency in biochemical pathways. Its hydration state contributes to solubility and stability, while the presence of multiple phosphate groups allows for intricate regulatory mechanisms in cellular processes. The compound's reactivity is influenced by its ability to form stable complexes with metal ions, impacting reaction dynamics. | ||||||
WIN 64338 hydrochloride | 163727-74-0 | sc-204398 sc-204398A | 1 mg 5 mg | $209.00 $852.00 | 1 | |
WIN 64338 hydrochloride is a phosphorus compound notable for its role in modulating biochemical pathways through specific molecular interactions. Its structure allows for the formation of transient intermediates, which can influence reaction kinetics and enhance selectivity in enzymatic processes. The compound's unique ability to engage in hydrogen bonding and coordinate with various substrates contributes to its reactivity profile, making it a key player in complex biochemical networks. | ||||||
Diethyl (4-Iodobenzyl)phosphonate | 173443-43-1 | sc-294316 sc-294316A | 5 g 25 g | $205.00 $667.00 | ||
Diethyl (4-Iodobenzyl)phosphonate is a phosphorus compound characterized by its ability to participate in nucleophilic substitution reactions, driven by the presence of the iodobenzyl group. This compound exhibits unique reactivity due to its phosphonate moiety, which can stabilize negative charges during reaction pathways. Its steric and electronic properties facilitate interactions with electrophiles, enhancing its role in organic synthesis and catalysis. The compound's versatility in forming stable complexes further underscores its significance in various chemical transformations. | ||||||
TPMPA | 182485-36-5 | sc-204352 sc-204352A | 10 mg 50 mg | $301.00 $847.00 | 1 | |
TPMPA is a phosphorus compound notable for its role as a versatile ligand in coordination chemistry. Its unique structure allows for strong interactions with metal ions, forming stable complexes that can influence reaction pathways. The presence of multiple functional groups enhances its reactivity, enabling it to participate in diverse chemical transformations. Additionally, TPMPA exhibits distinct solubility characteristics, which can affect its behavior in various solvent systems, making it a valuable tool in synthetic methodologies. | ||||||
(+)-1,2-Bis((2S,5S)-2,5-diphenylphospholano)ethane | 824395-67-7 | sc-222785 sc-222785A sc-222785B | 100 mg 500 mg 2 g | $104.00 $406.00 $1533.00 | ||
(+)-1,2-Bis((2S,5S)-2,5-diphenylphospholano)ethane is a phosphorus compound distinguished by its chiral phospholane framework, which facilitates selective metal coordination. This compound exhibits unique stereoelectronic properties, allowing for tailored reactivity in asymmetric synthesis. Its ability to stabilize transition states enhances reaction kinetics, while its solvation dynamics can significantly influence catalytic efficiency. The compound's robust ligand field strength further contributes to its effectiveness in metal-mediated transformations. | ||||||
(S,S)-1-Naphthyl-DIPAMP | sc-301725 | 100 mg | $120.00 | |||
(S,S)-1-Naphthyl-DIPAMP is a chiral phosphorus compound characterized by its unique naphthyl substituents, which enhance π-π stacking interactions and steric hindrance. This structure promotes selective coordination with transition metals, facilitating enantioselective catalysis. Its distinct electronic properties allow for fine-tuning of reaction pathways, while the compound's ability to stabilize reactive intermediates plays a crucial role in optimizing reaction rates and selectivity in various catalytic processes. | ||||||
Dichlorvos | 62-73-7 | sc-207557 | 250 mg | $41.00 | 1 | |
Dichlorvos is a phosphorus compound notable for its unique reactivity profile, particularly its ability to undergo nucleophilic substitution reactions. The presence of two chlorine atoms enhances its electrophilic character, allowing it to interact readily with nucleophiles. This compound exhibits significant stability under ambient conditions, yet can rapidly hydrolyze in the presence of water, leading to the formation of less toxic byproducts. Its molecular structure facilitates specific interactions with biological systems, influencing its kinetic behavior in various chemical environments. | ||||||
Tritolyl phosphate, mixture of isomers | 78-30-8 | sc-237406 | 500 ml | $39.00 | ||
Tritolyl phosphate, a mixture of isomers, is characterized by its complex molecular interactions and unique steric effects due to its bulky trityl groups. This compound exhibits distinct reactivity patterns, particularly in esterification and phosphorylation reactions, where it can act as a versatile electrophile. Its diverse isomeric forms contribute to varied solubility and viscosity, influencing its behavior in different chemical environments. Additionally, Tritolyl phosphate demonstrates interesting thermal stability, making it a subject of study in reaction kinetics and mechanistic pathways. | ||||||
Methyl dichlorophosphate | 677-24-7 | sc-235818 | 25 g | $152.00 | ||
Methyl dichlorophosphate is a reactive phosphorus compound known for its electrophilic nature, particularly in nucleophilic substitution reactions. Its structure allows for significant molecular interactions, facilitating the formation of stable intermediates. The compound exhibits unique reactivity as an acid halide, engaging in acylation processes that can lead to diverse products. Its distinct polar characteristics influence solubility and reactivity in various solvents, making it a subject of interest in synthetic chemistry. | ||||||
N,N-Bis(phosphonomethyl)glycine | 2439-99-8 | sc-253134 | 10 g | $115.00 | ||
N,N-Bis(phosphonomethyl)glycine is a versatile phosphorus compound characterized by its dual phosphonate groups, which enhance its ability to form chelates with metal ions. This chelation can significantly alter reaction kinetics, promoting unique pathways in various chemical processes. The compound's polar nature contributes to its solubility in aqueous environments, facilitating interactions with biological systems and influencing its behavior in complexation reactions. Its structural features enable it to participate in diverse coordination chemistry applications. | ||||||