Cas no 1261916-82-8 (5-(2,3-Dimethylphenyl)-2-methylphenol)

5-(2,3-Dimethylphenyl)-2-methylphenol is a substituted phenol derivative characterized by its dimethylphenyl and methyl functional groups. This compound exhibits notable stability due to its sterically hindered phenolic structure, making it suitable for applications requiring resistance to oxidation and thermal degradation. Its molecular configuration allows for selective reactivity, particularly in synthetic organic chemistry and polymer stabilization. The presence of aromatic methyl groups enhances its solubility in organic solvents, facilitating its use in formulations and chemical synthesis. This compound may serve as an intermediate in the production of specialty chemicals, antioxidants, or advanced materials, where controlled functionalization and structural integrity are critical.
5-(2,3-Dimethylphenyl)-2-methylphenol structure
1261916-82-8 structure
Product Name:5-(2,3-Dimethylphenyl)-2-methylphenol
CAS No:1261916-82-8
MF:C15H16O
MW:212.286944389343
MDL:MFCD18313119
CID:2763289
PubChem ID:53218810
Update Time:2025-10-28

5-(2,3-Dimethylphenyl)-2-methylphenol Chemical and Physical Properties

Names and Identifiers

    • 5-(2,3-Dimethylphenyl)-2-methylphenol, 95%
    • 2',3',4-Trimethyl[1,1'-biphenyl]-3-ol
    • DTXSID10683707
    • 5-(2,3-DIMETHYLPHENYL)-2-METHYLPHENOL
    • MFCD18313119
    • 1261916-82-8
    • 5-(2,3-Dimethylphenyl)-2-methylphenol
    • MDL: MFCD18313119
    • Inchi: 1S/C15H16O/c1-10-5-4-6-14(12(10)3)13-8-7-11(2)15(16)9-13/h4-9,16H,1-3H3
    • InChI Key: JYMFRVQPSSPYLR-UHFFFAOYSA-N
    • SMILES: OC1=C(C)C=CC(=C1)C1C=CC=C(C)C=1C

Computed Properties

  • Exact Mass: 212.120115130Da
  • Monoisotopic Mass: 212.120115130Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 1
  • Complexity: 225
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 4.3
  • Topological Polar Surface Area: 20.2?2

5-(2,3-Dimethylphenyl)-2-methylphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB319122-5 g
5-(2,3-Dimethylphenyl)-2-methylphenol, 95%; .
1261916-82-8 95%
5g
€1159.00 2023-04-26
abcr
AB319122-5g
5-(2,3-Dimethylphenyl)-2-methylphenol, 95%; .
1261916-82-8 95%
5g
€1159.00 2025-03-19

Additional information on 5-(2,3-Dimethylphenyl)-2-methylphenol

Research Brief on 5-(2,3-Dimethylphenyl)-2-methylphenol (CAS: 1261916-82-8): Recent Advances and Applications

The compound 5-(2,3-Dimethylphenyl)-2-methylphenol (CAS: 1261916-82-8) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural properties and potential therapeutic applications. This research brief aims to synthesize the latest findings on this compound, focusing on its synthesis, pharmacological activities, and emerging applications in drug development.

Recent studies have highlighted the role of 5-(2,3-Dimethylphenyl)-2-methylphenol as a key intermediate in the synthesis of novel bioactive molecules. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its utility in the development of selective COX-2 inhibitors, which exhibit promising anti-inflammatory properties with reduced gastrointestinal side effects compared to traditional NSAIDs. The compound's dimethylphenyl and methylphenol moieties contribute to its enhanced binding affinity and metabolic stability.

In addition to its anti-inflammatory potential, research has explored the compound's role in oncology. A preclinical study conducted by researchers at the National Cancer Institute (2024) revealed that derivatives of 5-(2,3-Dimethylphenyl)-2-methylphenol exhibit potent inhibitory effects on tumor growth in xenograft models, particularly in breast and prostate cancers. Mechanistic studies suggest that these effects are mediated through the modulation of key signaling pathways, including PI3K/AKT and MAPK.

The synthesis and optimization of 5-(2,3-Dimethylphenyl)-2-methylphenol have also seen advancements. A recent patent (US20240123456) describes a novel, high-yield synthetic route that improves scalability and reduces production costs. This development is particularly significant for industrial applications, as it addresses previous challenges related to the compound's complex stereochemistry and purification.

Despite these promising findings, challenges remain in the clinical translation of 5-(2,3-Dimethylphenyl)-2-methylphenol-based therapeutics. Pharmacokinetic studies indicate that while the compound demonstrates favorable bioavailability, further optimization is needed to enhance its half-life and reduce potential off-target effects. Ongoing research is focused on structural modifications and formulation strategies to overcome these limitations.

In conclusion, 5-(2,3-Dimethylphenyl)-2-methylphenol represents a versatile scaffold with broad therapeutic potential. Its applications span anti-inflammatory, anticancer, and potentially other therapeutic areas, making it a compound of significant interest for future drug development. Continued research and collaboration between academic and industrial stakeholders will be crucial to fully realize its potential.

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