Sulfur Compounds
Items 251 to 255 of 255 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Allyl phenyl sulfone | 16212-05-8 | sc-252362 | 5 g | $140.00 | ||
Allyl phenyl sulfone is a notable sulfur compound characterized by its sulfone functional group, which enhances its polarity and solubility in organic solvents. This compound exhibits unique reactivity in electrophilic aromatic substitution due to the electron-withdrawing nature of the sulfone, facilitating the formation of sulfonyl derivatives. Its ability to engage in Michael additions and participate in radical reactions highlights its versatility in synthetic pathways, making it an intriguing subject for further exploration in organic chemistry. | ||||||
Dimethylthiocarbamoyl chloride | 16420-13-6 | sc-252743 sc-252743A | 25 g 1 kg | $84.00 $450.00 | ||
Dimethylthiocarbamoyl chloride is a distinctive sulfur compound known for its highly reactive thiocarbamoyl group, which acts as a potent electrophile. This compound readily participates in acylation reactions, enabling the formation of thiocarbamoyl derivatives through nucleophilic substitution. Its unique electronic properties promote rapid reaction kinetics, while its polar nature enhances solubility in various organic solvents, making it an effective reagent in synthetic organic chemistry. | ||||||
Nitromethyl phenyl sulfone | 21272-85-5 | sc-253195 | 1 g | $96.00 | ||
Nitromethyl phenyl sulfone is a notable sulfur compound characterized by its nitro and sulfone functional groups, which impart unique electronic properties. The electron-withdrawing nitro group enhances the electrophilicity of the sulfone, facilitating nucleophilic attack in various reactions. Its polar nature contributes to strong intermolecular interactions, influencing solubility and reactivity in polar solvents. This compound exhibits distinct pathways in oxidation and reduction processes, showcasing its versatility in synthetic applications. | ||||||
1,2-Ethanedithiobis(trimethylsilane) | 51048-29-4 | sc-251559 | 5 ml | $79.00 | ||
1,2-Ethanedithiobis(trimethylsilane) is a distinctive sulfur compound featuring two thiol groups linked by a dithiobis structure. This configuration enables robust disulfide bond formation, influencing its reactivity in redox processes. The presence of trimethylsilyl groups enhances its stability and solubility in organic solvents, facilitating nucleophilic substitution reactions. Its unique electronic properties allow for selective interactions with electrophiles, making it a versatile reagent in synthetic chemistry. | ||||||
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. | ||||||