• 1. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
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• 2. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
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• 5. Enabling non-flammable Li-metal batteries via electrolyte functionalization and interface engineering?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzenesulfonamides

Comprehensive Guide to 2-(Morpholinosulfonyl)phenylmethanol (CAS No. 937796-15-1): Properties, Applications, and Market Insights

2-(Morpholinosulfonyl)phenylmethanol (CAS No. 937796-15-1) is a specialized organic compound with a unique molecular structure combining a phenyl ring, a sulfonyl group, and a morpholine moiety. This compound has garnered significant attention in pharmaceutical and chemical research due to its versatile properties. Researchers often search for "2-(Morpholinosulfonyl)phenylmethanol uses" or "CAS 937796-15-1 applications" to understand its potential in drug development and material science.

The molecular formula of 2-(Morpholinosulfonyl)phenylmethanol is C₁₁H₁₅NO₄S, with a molecular weight of 257.31 g/mol. Its structure features a hydroxymethyl group attached to a benzene ring, which is further substituted with a morpholinosulfonyl group. This configuration contributes to its solubility in polar organic solvents, making it valuable for synthetic chemistry applications. Common queries like "2-(Morpholinosulfonyl)phenylmethanol solubility" reflect the compound's practical utility in laboratory settings.

In pharmaceutical research, 2-(Morpholinosulfonyl)phenylmethanol serves as a key intermediate in the synthesis of biologically active molecules. Its structural motifs are particularly relevant in developing kinase inhibitors and other therapeutic agents. Recent trends show increased searches for "2-(Morpholinosulfonyl)phenylmethanol in drug discovery" as researchers explore its potential in targeted therapies. The compound's ability to modulate protein-protein interactions makes it valuable for studying signal transduction pathways.

The synthesis of 2-(Morpholinosulfonyl)phenylmethanol typically involves the reaction of appropriate phenyl precursors with morpholine derivatives under controlled conditions. Process optimization questions such as "synthesis of CAS 937796-15-1" frequently appear in chemical forums, indicating the compound's importance in synthetic methodology development. Advanced techniques like column chromatography are often employed for purification to achieve high purity grades required for research applications.

From a commercial perspective, the global market for 2-(Morpholinosulfonyl)phenylmethanol has shown steady growth, driven by increasing demand from pharmaceutical and biotechnology sectors. Market analysis queries like "2-(Morpholinosulfonyl)phenylmethanol suppliers" and "CAS 937796-15-1 price trends" reflect the compound's economic significance. Major chemical suppliers typically offer this compound in research quantities, with purity specifications ranging from 95% to 99% for different application requirements.

Recent scientific literature highlights novel applications of 2-(Morpholinosulfonyl)phenylmethanol in materials science, particularly in the development of functional polymers and coatings. Researchers investigating "2-(Morpholinosulfonyl)phenylmethanol in polymer chemistry" have discovered its potential as a modifying agent for surface properties. The compound's dual functionality allows for interesting material modifications while maintaining biocompatibility, making it suitable for medical device applications.

Quality control of 2-(Morpholinosulfonyl)phenylmethanol involves rigorous analytical techniques including HPLC, NMR spectroscopy, and mass spectrometry. Laboratory professionals often search for "CAS 937796-15-1 analytical methods" to ensure proper characterization of the compound. Standard reference spectra are available in major chemical databases, facilitating identification and purity assessment in research settings.

Environmental and safety considerations for handling 2-(Morpholinosulfonyl)phenylmethanol follow standard laboratory protocols for organic compounds. While not classified as hazardous under normal conditions, proper storage in cool, dry environments is recommended to maintain stability. Safety data sheets provide comprehensive information for researchers querying "2-(Morpholinosulfonyl)phenylmethanol safety" or "CAS 937796-15-1 handling".

The future research directions for 2-(Morpholinosulfonyl)phenylmethanol include exploration of its catalytic properties and potential in green chemistry applications. Emerging search trends like "2-(Morpholinosulfonyl)phenylmethanol in sustainable chemistry" indicate growing interest in environmentally friendly applications. Its structural features suggest possible utility in organocatalysis and as a building block for biodegradable materials.

For researchers and industry professionals, understanding the patent landscape surrounding 2-(Morpholinosulfonyl)phenylmethanol is crucial. Recent patent filings reveal innovative applications in electronic materials and specialty chemicals. Intellectual property searches for "CAS 937796-15-1 patents" have increased as companies explore proprietary uses of this versatile compound in advanced technologies.

• 941717-06-2(4-((2-(Bromomethyl)phenyl)sulfonyl)morpholine)
• 52601-77-1(1,7-Dioxa-4,10-diazacyclododecane,4,10-bis[(4-methylphenyl)sulfonyl]-)
• 646071-55-8([3-(morpholine-4-sulfonyl)phenyl]methanol)
• 852399-79-2((4-morpholinosulfonylphenyl)methanamine)
• 74461-33-9(1,4,10-Trioxa-7,13-diazacyclopentadecane,7,13-bis[(4-methylphenyl)sulfonyl]-)
• 96563-15-4(1,7-Dioxa-4,10-diazacyclododecane, 4-[(4-methylphenyl)sulfonyl]-)
• 300383-08-8(4-METHYL-3-(MORPHOLINE-4-SULFONYL)BENZOIC ACID)
• 862500-24-1(2-(morpholine-4-sulfonyl)benzaldehyde)
• 6339-26-0(4-Tosylmorpholine)
• 87223-34-5(2-(morpholine-4-sulfonyl)benzoic acid)