Sulfur Compounds
Items 251 to 255 of 255 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-Cyanophenyl isothiocyanate | 81431-98-3 | sc-283114 sc-283114A | 1 g 5 g | $51.00 $77.00 | ||
2-Cyanophenyl isothiocyanate is notable for its strong electrophilic nature, allowing it to readily participate in nucleophilic addition reactions. The presence of the isothiocyanate group facilitates the formation of thiourea derivatives through reaction with amines, showcasing its reactivity in forming stable covalent bonds. Additionally, its aromatic structure contributes to unique π-π stacking interactions, influencing its behavior in complexation and material science applications. | ||||||
2,3-Dichlorobenzenesulfonyl chloride | 82417-45-6 | sc-256278 | 5 g | $79.00 | ||
2,3-Dichlorobenzenesulfonyl chloride is a highly reactive acid chloride characterized by its dual chlorinated aromatic structure, which enhances its electrophilicity. This compound exhibits selective reactivity towards nucleophiles, particularly amines and alcohols, leading to the formation of sulfonamide linkages. The presence of the sulfonyl group not only stabilizes reaction intermediates but also influences the kinetics of acylation processes, making it a key player in synthetic organic chemistry. Its distinct polar nature allows for effective solvation in various organic solvents, further modulating its reactivity profile. | ||||||
2-(Trimethylsilyl)ethanesulfonamide | 125486-96-6 | sc-251681 | 1 g | $160.00 | ||
2-(Trimethylsilyl)ethanesulfonamide is characterized by its unique trimethylsilyl group, which enhances its nucleophilicity and facilitates various chemical transformations. This compound exhibits strong interactions with electrophiles, promoting rapid reaction kinetics in sulfonamide formation. Its sulfonamide moiety contributes to its stability and solubility in polar solvents, allowing for efficient participation in diverse synthetic pathways. The compound's ability to stabilize reactive intermediates further enhances its utility in organic synthesis. | ||||||
Methyl-2-isothiocyanatothiophene-3-carboxylate | 126637-07-8 | sc-286306 sc-286306A | 1 g 5 g | $155.00 $352.00 | ||
Methyl-2-isothiocyanatothiophene-3-carboxylate is a sulfur-containing compound notable for its isothiocyanate functional group, which enhances its electrophilic character. This compound engages in unique molecular interactions, particularly with nucleophiles, leading to diverse reaction pathways. Its thiophene ring contributes to aromatic stability, while the carboxylate moiety can participate in various chemical transformations, influencing reaction rates and selectivity in synthetic applications. | ||||||
S-Acetylthioglycolic acid pentafluorophenyl ester | 129815-48-1 | sc-253446 | 500 mg | $90.00 | ||
S-Acetylthioglycolic acid pentafluorophenyl ester is a versatile sulfur compound known for its reactivity as an acid halide. Its unique pentafluorophenyl ester moiety enhances electrophilicity, facilitating nucleophilic attack in various organic transformations. The compound exhibits rapid reaction kinetics, particularly in acylation processes, and its strong electron-withdrawing fluorine atoms contribute to distinctive molecular interactions, influencing solubility and stability in diverse chemical environments. | ||||||