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Comprehensive Overview of 4-(Benzylsulfanyl)benzoic Acid (CAS No. 22855-95-4): Properties, Applications, and Research Insights

4-(Benzylsulfanyl)benzoic Acid (CAS No. 22855-95-4) is a sulfur-containing aromatic carboxylic acid derivative that has garnered significant attention in pharmaceutical and materials science research. This compound, characterized by its benzylsulfanyl and benzoic acid functional groups, exhibits unique chemical properties that make it valuable for diverse applications. With the growing interest in sulfur-containing compounds and their role in drug discovery, this molecule is frequently searched in academic and industrial databases.

The molecular structure of 4-(Benzylsulfanyl)benzoic Acid features a thioether linkage (-S-CH₂-), which contributes to its stability and reactivity. Researchers often explore its potential as a building block for synthesizing more complex molecules, particularly in the development of bioactive compounds. Recent studies highlight its utility in peptide modification and polymer chemistry, aligning with the trending focus on sustainable and functional materials.

In the context of green chemistry, 4-(Benzylsulfanyl)benzoic Acid is investigated for its role in catalysis and organic transformations. Its compatibility with microwave-assisted synthesis and solvent-free reactions addresses the demand for eco-friendly protocols. Additionally, its photophysical properties are of interest for optoelectronic applications, a hot topic in materials science.

From a commercial perspective, suppliers often list this compound under keywords like "high-purity 4-(Benzylsulfanyl)benzoic Acid" or "CAS 22855-95-4 for research." FAQs in scientific forums frequently inquire about its solubility (e.g., in DMSO or ethanol), storage conditions, and handling precautions, reflecting practical user concerns. Analytical techniques such as HPLC, NMR, and mass spectrometry are typically employed for quality verification.

Emerging trends also link 4-(Benzylsulfanyl)benzoic Acid to metal-organic frameworks (MOFs) and coordination polymers, where its carboxylate group facilitates metal binding. This aligns with the surge in nanotechnology searches. Furthermore, its potential as a ligand in transition-metal catalysis is a subject of ongoing exploration, catering to the industrial demand for efficient catalytic systems.

In summary, 4-(Benzylsulfanyl)benzoic Acid (CAS No. 22855-95-4) bridges multiple disciplines, from medicinal chemistry to advanced materials. Its versatility and relevance to contemporary research themes ensure its continued prominence in scientific literature and commercial catalogs.

• 85654-13-3(Benzoic acid, 4-[[(3,4-dimethylphenyl)thio]methyl]-)
• 104351-51-1(2-(4-Methylbenzyl)sulfanylbenzenecarboxylic Acid)
• 88382-50-7(Benzoic acid, 4-[[(4-methylphenyl)thio]methyl]-)
• 1531-80-2(2-(benzylsulfanyl)benzoic acid)
• 13205-49-7(4-(Ethylthio)benzoic Acid)
• 88382-49-4(4-(Phenylsulfanyl)methylbenzoic Acid)
• 88393-07-1(Benzoic acid,4-[(phenylthio)methyl]-, methyl ester)
• 1699-03-2(2-(Phenylsulfanyl)methylbenzenecarboxylic Acid)
• 5537-74-6(3-(ethylsulfanyl)benzoic acid)
• 88382-51-8(4-(4-Chloro-phenylsulfanylmethyl)-benzoic acid)