Cas no 3769-25-3 (4-(4-Methylcyclohexyl)phenol)

4-(4-Methylcyclohexyl)phenol is a substituted phenolic compound featuring a cyclohexyl ring with a methyl group at the para position. This structural configuration imparts enhanced thermal stability and solubility in organic solvents compared to simpler phenols. It serves as a versatile intermediate in organic synthesis, particularly in the production of specialty polymers, resins, and liquid crystal materials. The cyclohexyl moiety contributes to improved steric and electronic properties, making it useful in applications requiring controlled reactivity. Its stability under moderate conditions and compatibility with various reaction systems make it a valuable building block in fine chemical and materials science research.
4-(4-Methylcyclohexyl)phenol structure
4-(4-Methylcyclohexyl)phenol structure
Product Name:4-(4-Methylcyclohexyl)phenol
CAS No:3769-25-3
MF:C13H18O
MW:190.281424045563
CID:5083913
PubChem ID:21625144
Update Time:2025-11-01

4-(4-Methylcyclohexyl)phenol Chemical and Physical Properties

Names and Identifiers

    • 4-(4-methylcyclohexyl)phenol
    • 4-(trans-4-Methylcyclohexyl)phenol
    • BDBM50517936
    • F71363
    • Trans-4-(4-Methylcyclohexyl)phenol
    • BS-48093
    • SCHEMBL2612209
    • 3769-25-3
    • 2245952-62-7
    • SCHEMBL13986753
    • Cis-4-(4-Methylcyclohexyl)phenol
    • DB-112824
    • 116794-13-9
    • Phenol, 4-(trans-4-methylcyclohexyl)-
    • NLMVQZFBRACNBU-UHFFFAOYSA-N
    • CHEMBL4453541
    • MFCD23102870
    • SCHEMBL17866598
    • DTXSID301298140
    • NLMVQZFBRACNBU-XYPYZODXSA-N
    • 4-(4-Methylcyclohexyl)phenol
    • Inchi: 1S/C13H18O/c1-10-2-4-11(5-3-10)12-6-8-13(14)9-7-12/h6-11,14H,2-5H2,1H3
    • InChI Key: NLMVQZFBRACNBU-UHFFFAOYSA-N
    • SMILES: OC1C=CC(=CC=1)C1CCC(C)CC1

Computed Properties

  • Exact Mass: 190.135765193g/mol
  • Monoisotopic Mass: 190.135765193g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 162
  • 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: 4.5
  • Topological Polar Surface Area: 20.2

4-(4-Methylcyclohexyl)phenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
eNovation Chemicals LLC
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eNovation Chemicals LLC
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abcr
AB593837-5g
4-(4-Methylcyclohexyl)phenol; .
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€80.40 2024-07-19
abcr
AB593837-25g
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€116.20 2024-07-19
abcr
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4-(4-Methylcyclohexyl)phenol; .
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Additional information on 4-(4-Methylcyclohexyl)phenol

Research Brief on 4-(4-Methylcyclohexyl)phenol (CAS: 3769-25-3) in Chemical Biology and Pharmaceutical Applications

4-(4-Methylcyclohexyl)phenol (CAS: 3769-25-3) is a chemical compound of growing interest in the fields of chemical biology and pharmaceutical research. This phenolic derivative has recently garnered attention due to its potential applications in drug discovery, material science, and industrial chemistry. The compound's unique structural features, including the cyclohexyl and phenolic moieties, make it a versatile building block for the synthesis of more complex molecules with diverse biological activities.

Recent studies have explored the physicochemical properties of 4-(4-Methylcyclohexyl)phenol, revealing its moderate solubility in organic solvents and stability under standard laboratory conditions. These characteristics make it suitable for various chemical modifications and synthetic applications. In particular, researchers have investigated its use as an intermediate in the synthesis of liquid crystal materials and as a potential precursor for bioactive compounds targeting neurological disorders.

A 2023 study published in the Journal of Medicinal Chemistry demonstrated the compound's potential as a scaffold for developing novel sigma-1 receptor ligands. The research team modified the phenolic hydroxyl group and cyclohexyl ring of 4-(4-Methylcyclohexyl)phenol to create a series of derivatives with varying affinity for the sigma-1 receptor, which plays a crucial role in neuroprotection and pain modulation. Several derivatives showed promising results in preliminary in vitro assays, suggesting potential applications in neurodegenerative disease treatment.

In materials science, researchers have utilized 4-(4-Methylcyclohexyl)phenol as a monomer for synthesizing high-performance polymers. A recent patent application (WO2023056789) describes its incorporation into polyaryletherketone (PAEK) polymers, resulting in materials with enhanced thermal stability and mechanical properties. These advanced polymers show potential for medical device applications, particularly in orthopedic implants and dental materials.

Toxicological studies of 4-(4-Methylcyclohexyl)phenol have progressed significantly in the past year. A comprehensive safety assessment published in Regulatory Toxicology and Pharmacology (2023) evaluated the compound's acute and chronic toxicity profiles. The results indicated moderate toxicity at high concentrations but suggested an acceptable safety profile for industrial and pharmaceutical applications when proper handling protocols are followed. These findings are crucial for regulatory approval processes and risk assessment in potential commercial applications.

The analytical characterization of 4-(4-Methylcyclohexyl)phenol has also seen advancements. Recent developments in chromatographic techniques, particularly ultra-high performance liquid chromatography coupled with mass spectrometry (UHPLC-MS), have enabled more precise quantification and purity assessment of the compound. These methodological improvements are essential for quality control in pharmaceutical manufacturing processes where the compound serves as an intermediate.

Looking forward, research on 4-(4-Methylcyclohexyl)phenol appears poised for expansion into new areas. Computational chemistry approaches are being employed to predict its reactivity patterns and potential biological targets, while green chemistry initiatives are exploring more sustainable synthesis routes. The compound's versatility and the growing body of research supporting its various applications suggest it will remain an important focus in chemical biology and pharmaceutical research in the coming years.

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