Cas no 55163-71-8 (Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate))

Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) is a specialized organic compound featuring a benzeneethanol core substituted with a β-methoxy group and a 4-methylbenzenesulfonate ester. This structure imparts unique reactivity, making it valuable as an intermediate in organic synthesis, particularly for the preparation of protected alcohol derivatives or sulfonate esters. The 4-methylbenzenesulfonate (tosylate) group enhances its utility as a leaving group in nucleophilic substitution reactions, while the β-methoxy substitution can influence stereoelectronic properties. Its stability and well-defined reactivity profile make it suitable for controlled functionalization in pharmaceutical or fine chemical applications. Proper handling is required due to potential sensitivity to moisture and strong nucleophiles.
Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) structure
55163-71-8 structure
Product Name:Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate)
CAS No:55163-71-8
MF:C16H18O4S
MW:306.376723766327
CID:1592912
Update Time:2025-05-24

Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) Chemical and Physical Properties

Names and Identifiers

    • Benzeneethanol, b-methoxy-, 4-methylbenzenesulfonate
    • Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate)
    • Inchi: 1S/C16H18O4S/c1-13-8-10-15(11-9-13)21(17,18)20-12-16(19-2)14-6-4-3-5-7-14/h3-11,16H,12H2,1-2H3
    • InChI Key: SLGJXFGDRSSEBP-UHFFFAOYSA-N
    • SMILES: CC1C=CC(S(OCC(OC)C2C=CC=CC=2)(=O)=O)=CC=1

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Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) Related Literature

Additional information on Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate)

Comprehensive Overview of Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) (CAS No. 55163-71-8)

Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) (CAS No. 55163-71-8) is a specialized organic compound widely utilized in pharmaceutical intermediates, fragrance synthesis, and advanced material research. This compound, characterized by its unique methoxy and tosylate functional groups, has garnered significant attention in recent years due to its versatile applications in green chemistry and sustainable manufacturing processes. Researchers and industry professionals frequently search for terms like "β-methoxy benzeneethanol derivatives", "tosylate ester applications", and "CAS 55163-71-8 synthesis methods", reflecting its growing relevance in scientific and industrial domains.

The molecular structure of Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) combines a phenyl ring with an ethanol backbone, modified by a methoxy group at the β-position and a 4-methylbenzenesulfonate (tosylate) ester at the primary alcohol. This configuration enhances its reactivity in nucleophilic substitution reactions, making it a valuable precursor in the synthesis of complex molecules. Recent studies highlight its role in developing biodegradable polymers and non-toxic plasticizers, aligning with global trends toward eco-friendly materials. Keywords such as "green synthesis of tosylate esters" and "sustainable aromatic compounds" are increasingly associated with this compound in academic literature.

In the pharmaceutical sector, CAS 55163-71-8 serves as a key intermediate for designing drug delivery systems and prodrug formulations. Its tosylate group facilitates controlled release mechanisms, a feature highly sought after in precision medicine. Online queries like "benzeneethanol derivatives in drug development" and "methoxy-tosylate pharmacokinetics" underscore its therapeutic potential. Additionally, the compound’s stability under mild conditions makes it suitable for catalysis research, particularly in asymmetric synthesis—a hotspot in modern organic chemistry.

From an industrial perspective, Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) is employed in the production of high-performance lubricants and specialty coatings. Its ability to form stable thin films has led to innovations in nanotechnology applications, such as self-assembling monolayers (SAMs). Searches for "tosylate esters in material science" and "CAS 55163-71-8 industrial uses" reflect this demand. Furthermore, the compound’s compatibility with ionic liquids positions it as a candidate for energy storage solutions, a trending topic in renewable energy research.

Quality control and analytical methods for 55163-71-8 are critical discussion points. Techniques like HPLC, GC-MS, and NMR spectroscopy are commonly used to verify purity and structural integrity. Laboratories often search for "analytical standards for β-methoxy benzeneethanol" or "CAS 55163-71-8 spectral data", emphasizing the need for reliable characterization protocols. Regulatory compliance, particularly concerning REACH and FDA guidelines, is another frequent query, highlighting the compound’s adherence to international safety standards.

In conclusion, Benzeneethanol, β-methoxy-, 1-(4-methylbenzenesulfonate) (CAS No. 55163-71-8) represents a multifaceted compound with applications spanning pharmaceuticals, materials science, and sustainable chemistry. Its alignment with contemporary research trends—such as green synthesis, nanomaterials, and targeted therapeutics—ensures its continued prominence in scientific discourse. By addressing user-driven queries and integrating cutting-edge developments, this overview provides a holistic perspective on the compound’s significance and future potential.

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