Items 101 to 110 of 112 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Niobium(V) oxide | 1313-96-8 | sc-253190 sc-253190A | 10 g 50 g | $35.00 $108.00 | ||
Niobium(V) oxide exhibits unique electronic properties, making it a key material in advanced capacitors and superconductors. Its high dielectric constant enhances energy storage capabilities, while its layered structure allows for effective charge separation and transport. The compound's ability to form niobate structures facilitates electron mobility, contributing to its performance in high-frequency applications. Additionally, its chemical stability under varying conditions ensures reliable operation in electronic circuits. | ||||||
D-149 Dye | 786643-20-7 | sc-214800 | 100 mg | $349.00 | ||
D-149 Dye is a specialized compound known for its exceptional light absorption and photoconductive properties, making it ideal for electronic applications. Its unique molecular structure allows for efficient charge transfer, enhancing the performance of organic photodetectors. The dye's strong π-π stacking interactions contribute to its stability and facilitate exciton migration, while its tunable electronic properties enable customization for specific wavelengths, optimizing device efficiency. | ||||||
Astrophloxine | 14696-39-0 | sc-210842 sc-210842A | 5 mg 50 mg | $155.00 $1040.00 | ||
Astrophloxine is an innovative acid halide characterized by its unique electron-withdrawing properties, which enhance charge transfer in electronic systems. Its molecular structure facilitates rapid reaction kinetics, allowing for efficient cross-linking in polymer matrices. The compound's distinctive dipole interactions contribute to improved dielectric constants, making it suitable for high-performance capacitors and insulating layers. Additionally, its reactivity with various substrates promotes robust bonding, enhancing overall device stability. | ||||||
Trichloro(1H,1H,2H,2H-perfluorooctyl)silane | 78560-45-9 | sc-251303B sc-251303 sc-251303A | 1 g 10 g 50 g | $38.00 $100.00 $443.00 | ||
Trichloro(1H,1H,2H,2H-perfluorooctyl)silane is a specialized silane compound that exhibits remarkable hydrophobicity and low surface energy due to its perfluorinated tail. This unique structure promotes strong siloxane bond formation with substrates, enhancing adhesion and durability in electronic applications. Its ability to modify surface properties leads to improved dielectric performance and reduced friction, making it ideal for advanced electronic coatings and insulation materials. | ||||||
7-Ketocholesterol | 566-28-9 | sc-210630 | 5 mg | $99.00 | 5 | |
7-Ketocholesterol is a notable compound in electronics due to its unique ability to modulate electron mobility through specific molecular interactions. Its structural features enable effective charge transport, enhancing conductivity in organic semiconductors. The compound exhibits distinct photophysical properties, allowing for efficient light absorption and emission, which can be harnessed in optoelectronic applications. Furthermore, its reactivity with metal ions can facilitate the formation of conductive pathways, improving device performance. | ||||||
Trimethoxyphenylsilane | 2996-92-1 | sc-251346 sc-251346A | 50 ml 250 ml | $39.00 $91.00 | ||
Trimethoxyphenylsilane is a versatile compound in electronics, characterized by its ability to form robust siloxane networks that enhance adhesion and stability in various substrates. Its trimethoxy groups facilitate hydrolysis, leading to silanol formation, which promotes cross-linking and improved mechanical properties. The compound's unique surface chemistry allows for effective modification of electronic interfaces, optimizing charge transfer and reducing energy loss in devices. Additionally, its hydrophobic nature aids in moisture resistance, crucial for long-term performance. | ||||||
o-Carborane | 16872-09-6 | sc-228855 | 1 g | $112.00 | ||
o-Carborane is a unique compound in electronics, notable for its exceptional thermal stability and resistance to radiation. Its cage-like structure allows for strong molecular interactions, enhancing dielectric properties and minimizing leakage currents in electronic components. The compound's ability to form stable bonds with various substrates facilitates the development of advanced materials with tailored electrical characteristics. Furthermore, its low reactivity contributes to the longevity and reliability of electronic devices. | ||||||
Bromotris(triphenylphosphine)copper(I) | 15709-74-7 | sc-227535 | 5 g | $67.00 | ||
Bromotris(triphenylphosphine)copper(I) is a notable compound in electronics, recognized for its role as a catalyst in various organic reactions. Its unique coordination chemistry allows for efficient electron transfer processes, enhancing reaction kinetics in coupling reactions. The presence of triphenylphosphine ligands stabilizes the copper center, promoting selective reactivity. This compound's ability to facilitate complex molecular transformations makes it essential in the synthesis of advanced electronic materials. | ||||||
Gallium(II) telluride | 12024-14-5 | sc-279178 | 1 g | $176.00 | ||
Gallium(II) telluride is a semiconductor with intriguing electronic properties, characterized by its narrow bandgap and high carrier mobility. Its unique crystal structure enables efficient charge transport, making it suitable for optoelectronic applications. The compound exhibits strong light absorption and photoconductivity, facilitating the generation of excitons. Additionally, its anisotropic electrical properties allow for tailored device performance in advanced electronic systems. | ||||||
3,5-Bis(4-tert-butylphenyl)-4-phenyl-4H-1,2,4-triazole | 203799-76-2 | sc-252049 | 1 g | $151.00 | ||
3,5-Bis(4-tert-butylphenyl)-4-phenyl-4H-1,2,4-triazole is a notable compound in electronics due to its exceptional charge transfer capabilities and robust thermal stability. Its unique molecular architecture promotes effective π-π stacking interactions, enhancing electron mobility. The compound's ability to form stable radical cations under light exposure contributes to its photostability, making it ideal for organic electronic devices. Its tailored energy levels facilitate efficient exciton management, optimizing performance in various applications. | ||||||