Items 21 to 30 of 72 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Selenium Sulfide | 7488-56-4 | sc-296376 sc-296376A | 5 g 25 g | $50.00 $84.00 | ||
Selenium sulfide is a unique selenium compound characterized by its ability to undergo oxidation-reduction reactions, which can significantly alter its electronic properties. The compound's molecular structure allows for interactions with various substrates, enhancing its reactivity in diverse chemical environments. Its distinct physical properties, such as solubility in organic solvents, facilitate its participation in complexation reactions, potentially leading to the formation of novel selenium-based materials. | ||||||
Molybdenum(IV) selenide | 12058-18-3 | sc-269613 | 5 g | $126.00 | ||
Molybdenum(IV) selenide exhibits intriguing electronic and optical properties due to its layered structure, which allows for strong interlayer interactions. This compound can participate in charge transfer processes, enhancing its conductivity and making it a subject of interest in materials science. Its unique bonding characteristics enable it to form stable complexes with other elements, influencing reaction kinetics and pathways in various chemical systems. | ||||||
Benzeneseleninic acid anhydride | 17697-12-0 | sc-252414 | 1 g | $26.00 | ||
Benzeneseleninic acid anhydride is a notable selenium compound characterized by its reactivity as an acid halide. It readily undergoes nucleophilic acyl substitution, facilitating the formation of selenoesters and other derivatives. The compound's electrophilic nature allows it to engage in selective reactions with amines and alcohols, leading to diverse synthetic pathways. Its unique molecular structure contributes to distinct steric and electronic effects, influencing reaction rates and product distributions in organic synthesis. | ||||||
5-[2-(Ethylseleno)ethyl]hydantoin | sc-217107 | 100 mg | $300.00 | |||
5-[2-(Ethylseleno)ethyl]hydantoin is a distinctive selenium compound that exhibits unique reactivity patterns due to its hydantoin framework. This compound can participate in redox reactions, showcasing its ability to act as both an electron donor and acceptor. Its ethylseleno group enhances its nucleophilicity, allowing for selective interactions with electrophiles. Additionally, the compound's structural features promote specific conformational dynamics, influencing its stability and reactivity in various chemical environments. | ||||||
Boc-DL-selenomethionine | sc-326452 sc-326452A | 500 mg 1 g | $595.00 $982.00 | |||
Boc-DL-selenomethionine is a notable selenium compound characterized by its Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility in organic solvents. This compound exhibits unique coordination chemistry, allowing it to form stable complexes with metal ions. Its selenium atom can participate in diverse oxidation states, facilitating intriguing electron transfer processes. The presence of the Boc group also influences its steric hindrance, affecting reaction kinetics and selectivity in various chemical transformations. | ||||||
Boc-L-selenomethionine | sc-326466 sc-326466A | 500 mg 1 g | $490.00 $885.00 | |||
Boc-L-selenomethionine is a distinctive selenium compound featuring a Boc protecting group that imparts enhanced stability and solubility. This compound engages in unique molecular interactions due to the presence of selenium, which can adopt multiple oxidation states, enabling it to participate in redox reactions. The steric effects of the Boc group also play a crucial role in modulating reaction pathways and selectivity, influencing the kinetics of various chemical processes. | ||||||
Fmoc-DL-selenomethionine | sc-327782 sc-327782A | 500 mg 1 g | $584.00 $982.00 | |||
Fmoc-DL-selenomethionine is a notable selenium compound characterized by its Fmoc protecting group, which enhances its stability and solubility in organic solvents. The selenium atom introduces unique electronic properties, allowing for diverse coordination chemistry and interactions with metal ions. Its structure facilitates specific hydrogen bonding and π-π stacking interactions, influencing reaction dynamics and selectivity in synthetic pathways. The compound's distinct stereochemistry also affects its reactivity and molecular recognition processes. | ||||||
4-amino-2,1,3-benzoselenadiazol hydrochloride | sc-349067 sc-349067A | 250 mg 1 g | $188.00 $380.00 | |||
4-amino-2,1,3-benzoselenadiazol hydrochloride is a distinctive selenium compound featuring a selenadiazole core that imparts unique electronic characteristics. Its nitrogen and selenium atoms enable intriguing charge transfer interactions, enhancing its reactivity in various chemical environments. The compound exhibits notable photophysical properties, including fluorescence, which can be influenced by solvent polarity. Additionally, its ability to form stable complexes with transition metals opens avenues for exploring catalytic pathways and material science applications. | ||||||
Cobalt(II) selenide | 1307-99-9 | sc-268759 | 50 g | $285.00 | ||
Cobalt(II) selenide is a fascinating selenium compound characterized by its layered crystal structure, which facilitates unique electronic and optical properties. The interaction between cobalt and selenium atoms leads to distinct magnetic behavior, making it a subject of interest in materials science. Its semiconductor nature allows for intriguing charge carrier dynamics, while its reactivity with acids can yield various cobalt selenide derivatives, expanding its potential in diverse chemical reactions. | ||||||
Manganese(II) selenide | 1313-22-0 | sc-269380 | 1 g | $74.00 | ||
Manganese(II) selenide exhibits intriguing properties as a selenium compound, featuring a unique cubic crystal lattice that influences its electronic characteristics. The strong bonding interactions between manganese and selenium contribute to its notable photoluminescence and thermoelectric behavior. Additionally, its reactivity with halogens can lead to the formation of various manganese selenide complexes, enhancing its role in solid-state chemistry and materials research. | ||||||