Items 381 to 384 of 384 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Josiphos SL-J216-1 | 849924-43-2 | sc-500924 | 100 mg | $420.00 | ||
Arsenobetaine | 64436-13-1 | sc-227279 | 50 mg | $440.00 | ||
Arsenobetaine is a unique organometallic compound characterized by its stable arsenic-carbon bond, which exhibits remarkable resistance to oxidation. This stability allows for distinct molecular interactions, particularly in biological systems, where it can influence metabolic pathways. Its solubility in polar solvents enhances its reactivity, enabling specific coordination with metal ions. The compound's behavior in various environments provides insights into arsenic biochemistry and its role in environmental processes. | ||||||
(3-Mercaptopropyl)trimethoxysilane | 4420-74-0 | sc-231786 | 25 g | $30.00 | ||
(3-Mercaptopropyl)trimethoxysilane is an organometallic compound notable for its thiol functional group, which facilitates strong interactions with metal surfaces through sulfur coordination. This compound exhibits unique reactivity patterns, particularly in silane coupling reactions, enhancing adhesion properties in composite materials. Its trimethoxysilane groups promote hydrolysis and condensation, leading to the formation of siloxane networks. The compound's ability to form stable bonds with both organic and inorganic substrates makes it a versatile agent in surface modification and material science. | ||||||
Trioctylaluminum solution | 1070-00-4 | sc-237355 sc-237355A | 100 ml 500 ml | $77.00 $214.00 | ||
Trioctylaluminum solution is a versatile organometallic compound characterized by its unique alkyl chain structure, which enhances its reactivity and solubility in organic solvents. The presence of aluminum facilitates Lewis acid behavior, promoting electrophilic interactions that can activate substrates for various reactions. Its ability to form stable complexes with ligands influences catalytic pathways, while the steric bulk of the octyl groups modulates reactivity, allowing for selective transformations in synthetic applications. | ||||||