Items 11 to 20 of 255 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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3-(5-Chloro-2,4-dimethoxy-phenylsulfamoyl)-4-methoxy-benzoic acid | sc-345700 sc-345700A | 1 g 5 g | $266.00 $800.00 | |||
3-(5-Chloro-2,4-dimethoxy-phenylsulfamoyl)-4-methoxy-benzoic acid showcases distinctive behavior as a sulfur compound, particularly through its capacity for electrophilic aromatic substitution. The sulfonamide group enhances electron-withdrawing effects, promoting reactivity in nucleophilic attack scenarios. Its methoxy substituents contribute to solubility and polarity, influencing intermolecular interactions. The chloro group adds a layer of steric hindrance, potentially altering reaction kinetics and selectivity in synthetic transformations. | ||||||
2-[(2-methylpropane)sulfonyl]acetic acid | sc-340595 sc-340595A | 250 mg 1 g | $248.00 $510.00 | |||
2-[(2-methylpropane)sulfonyl]acetic acid features a sulfonyl group that enhances its reactivity, allowing for unique electrophilic interactions in various chemical environments. The compound's acidic nature facilitates proton transfer, influencing reaction kinetics and equilibrium. Its branched structure contributes to steric hindrance, which can modulate reactivity and selectivity in nucleophilic attacks. Additionally, the sulfonyl moiety can engage in dipole-dipole interactions, further affecting solubility and reactivity profiles in diverse chemical systems. | ||||||
3-[(trifluoromethyl)thio]propanoic acid | sc-344837 sc-344837A | 250 mg 1 g | $248.00 $510.00 | |||
3-[(Trifluoromethyl)thio]propanoic acid is characterized by its trifluoromethyl group, which significantly influences its electronic properties and enhances its acidity. The sulfur atom introduces unique polarizability, facilitating strong intermolecular interactions. This compound can engage in electrophilic substitution reactions, and its distinct steric effects can modulate reaction pathways. Additionally, the presence of the trifluoromethyl group can stabilize reactive intermediates, impacting overall reaction kinetics. | ||||||
5-(4-Phenoxy-phenylamino)-[1,3,4]thiadiazole-2-thiol | sc-350142 sc-350142A | 1 g 5 g | $266.00 $800.00 | |||
5-(4-Phenoxy-phenylamino)-[1,3,4]thiadiazole-2-thiol features a distinctive thiadiazole framework that contributes to its rich electronic properties, enabling effective charge transfer. The compound's sulfur atom plays a pivotal role in forming strong hydrogen bonds, enhancing its solubility in polar solvents. Additionally, the interplay between the thiol and aromatic substituents allows for diverse coordination chemistry, potentially leading to unique complexation behaviors with metal ions. | ||||||
2-(3-Chloro-phenyl)-ethanesulfonyl chloride | 728919-59-3 | sc-320567 | 1 g | $745.00 | ||
2-(3-Chloro-phenyl)-ethanesulfonyl chloride is a versatile acid halide characterized by its strong electrophilic nature, enabling rapid acylation reactions with nucleophiles. The presence of the sulfonyl chloride group enhances its reactivity, facilitating the formation of sulfonamides and other derivatives. Its chlorophenyl substituent can engage in π-stacking interactions, influencing reaction kinetics and selectivity. This compound's unique electronic properties allow for tailored reactivity in various synthetic pathways. | ||||||
MTSL | 81213-52-7 | sc-208677 sc-208677A | 10 mg 50 mg | $167.00 $653.00 | 56 | |
MTSL is a versatile sulfur compound known for its unique electron-donating properties, which enhance its reactivity in various chemical environments. Its ability to form stable adducts with transition metals facilitates diverse coordination chemistry. MTSL exhibits distinct pathways in redox reactions, often participating in electron transfer processes that influence reaction kinetics. Additionally, its molecular structure allows for specific interactions with nucleophiles, making it a key player in sulfur-based transformations. | ||||||
β-Mercaptoethanol | 60-24-2 | sc-202966A sc-202966 | 100 ml 250 ml | $88.00 $118.00 | 10 | |
β-Mercaptoethanol is a thiol compound characterized by its strong nucleophilic properties, enabling it to readily participate in redox reactions. The presence of the thiol group allows for the formation of disulfide bonds, which play a crucial role in protein folding and stabilization. Its ability to donate protons makes it a versatile reducing agent, while its polar nature enhances solubility in aqueous environments, facilitating interactions with various biomolecules. | ||||||
Sulfosuccinimidyl oleate sodium | 135661-44-8 | sc-208408B sc-208408 sc-208408A sc-208408C | 10 mg 25 mg 50 mg 250 mg | $240.00 $410.00 $720.00 $2856.00 | 17 | |
Sulfosuccinimidyl oleate sodium is a sulfonate compound characterized by its amphiphilic nature, which facilitates unique interactions with lipid membranes. Its structure promotes self-assembly into micelles, enhancing its ability to modulate surface tension. The compound exhibits distinct reaction kinetics, particularly in nucleophilic substitution reactions, where its sulfonate group can act as a leaving group, influencing the rate and pathway of chemical transformations. | ||||||
(±)-S-Nitroso-N-acetylpenicillamine | 79032-48-7 | sc-200319B sc-200319 sc-200319A | 10 mg 20 mg 100 mg | $73.00 $112.00 $367.00 | 18 | |
(±)-S-Nitroso-N-acetylpenicillamine, a sulfur compound, showcases intriguing redox properties stemming from its nitroso and thiol functionalities. The compound participates in unique electron transfer processes, allowing it to act as a versatile signaling molecule. Its ability to form stable adducts with metal ions enhances its reactivity, while the presence of the acetyl group influences steric hindrance, affecting reaction pathways and selectivity in various chemical transformations. | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | $150.00 $286.00 $479.00 $1299.00 $8299.00 $915.00 | 22 | |
D,L-Sulforaphane is a sulfur-containing compound notable for its electrophilic nature, which enables it to interact with various biological nucleophiles. Its unique structure allows for the formation of covalent bonds with proteins, influencing cellular signaling pathways. The compound exhibits a high reactivity profile, particularly in Michael addition reactions, and its stability is enhanced by the presence of a thiol group, which can participate in redox reactions, further modulating its biological activity. |