Cas no 328125-42-4 (3-(5-Cyanopyridin-3-yl)benzyl alcohol)

3-(5-Cyanopyridin-3-yl)benzyl alcohol is a versatile intermediate in organic synthesis, particularly valued for its bifunctional structure combining a cyanopyridine moiety with a benzyl alcohol group. This compound serves as a key building block in pharmaceutical and agrochemical research, enabling the development of heterocyclic compounds with potential biological activity. Its reactive cyanopyridine group facilitates further functionalization, while the benzyl alcohol moiety offers additional derivatization opportunities. The compound’s stability and purity make it suitable for high-precision applications in medicinal chemistry and material science. Its structural features are advantageous for designing ligands, catalysts, and bioactive molecules, underscoring its utility in advanced synthetic workflows.
3-(5-Cyanopyridin-3-yl)benzyl alcohol structure
328125-42-4 structure
Product Name:3-(5-Cyanopyridin-3-yl)benzyl alcohol
CAS No:328125-42-4
MF:C13H13NO2
MW:215.247823476791
CID:917309
PubChem ID:56604783
Update Time:2025-10-30

3-(5-Cyanopyridin-3-yl)benzyl alcohol Chemical and Physical Properties

Names and Identifiers

    • 3-(5-Cyanopyridin-3-yl)benzyl alcohol
    • 5-[3-(hydroxymethyl)phenyl]pyridine-3-carbonitrile
    • [4-(6-methoxy-pyridin-3-yl)-phenyl]-methanol
    • 4-(2-methoxy-pyridin-5-yl)-benzyl alcohol
    • SCHEMBL3059303
    • (4-(6-Methoxypyridin-3-yl)phenyl)methanol
    • 328125-42-4
    • FUQDBAPDOHYSSI-UHFFFAOYSA-N
    • 4-(6-Methoxypyridin-3-yl)benzyl alcohol
    • MDL: MFCD20441473
    • Inchi: 1S/C13H13NO2/c1-16-13-7-6-12(8-14-13)11-4-2-10(9-15)3-5-11/h2-8,15H,9H2,1H3
    • InChI Key: FUQDBAPDOHYSSI-UHFFFAOYSA-N
    • SMILES: OCC1C=CC(=CC=1)C1C=NC(=CC=1)OC

Computed Properties

  • Exact Mass: 210.07900
  • Monoisotopic Mass: 215.094628657g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 202
  • 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: 1.9
  • Topological Polar Surface Area: 42.4?2

Experimental Properties

  • PSA: 56.91000
  • LogP: 2.11258

3-(5-Cyanopyridin-3-yl)benzyl alcohol Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3-(5-Cyanopyridin-3-yl)benzyl alcohol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Crysdot LLC
CD11144520-1g
(4-(6-Methoxypyridin-3-yl)phenyl)methanol
328125-42-4 97%
1g
$370 2024-07-16

Additional information on 3-(5-Cyanopyridin-3-yl)benzyl alcohol

Recent Advances in the Study of 3-(5-Cyanopyridin-3-yl)benzyl alcohol (CAS: 328125-42-4) in Chemical Biology and Pharmaceutical Research

3-(5-Cyanopyridin-3-yl)benzyl alcohol (CAS: 328125-42-4) is a compound of significant interest in the field of chemical biology and pharmaceutical research due to its potential applications in drug discovery and development. Recent studies have explored its synthesis, biological activity, and mechanistic insights, positioning it as a promising candidate for therapeutic interventions. This research brief provides an overview of the latest findings related to this compound, highlighting its relevance and potential in modern medicine.

The synthesis of 3-(5-Cyanopyridin-3-yl)benzyl alcohol has been optimized in recent years, with researchers focusing on improving yield and purity. A study published in the Journal of Medicinal Chemistry (2023) detailed a novel catalytic method that enhances the efficiency of its production, reducing byproducts and increasing scalability. This advancement is critical for its potential use in large-scale pharmaceutical applications, where consistency and cost-effectiveness are paramount.

In terms of biological activity, 3-(5-Cyanopyridin-3-yl)benzyl alcohol has demonstrated notable inhibitory effects on specific enzymatic pathways. Research conducted at the University of Cambridge (2024) revealed its ability to modulate the activity of kinases involved in inflammatory responses. These findings suggest its potential as a lead compound for developing anti-inflammatory drugs, particularly for conditions like rheumatoid arthritis and inflammatory bowel disease.

Further mechanistic studies have elucidated the compound's interaction with cellular targets. A recent paper in Nature Chemical Biology (2024) utilized X-ray crystallography to map the binding site of 3-(5-Cyanopyridin-3-yl)benzyl alcohol within a key protein structure. This structural insight provides a foundation for rational drug design, enabling researchers to optimize the compound's affinity and selectivity for therapeutic purposes.

The pharmacokinetic properties of 3-(5-Cyanopyridin-3-yl)benzyl alcohol have also been investigated, with promising results. A preclinical study published in Drug Metabolism and Disposition (2023) reported favorable absorption and distribution profiles in animal models, alongside minimal toxicity. These characteristics enhance its viability as a drug candidate, though further clinical trials are necessary to confirm its safety and efficacy in humans.

In conclusion, 3-(5-Cyanopyridin-3-yl)benzyl alcohol (CAS: 328125-42-4) represents a compound of growing importance in pharmaceutical research. Its optimized synthesis, biological activity, and mechanistic insights underscore its potential as a therapeutic agent. Future research should focus on translational studies to bridge the gap between laboratory findings and clinical applications, paving the way for its integration into modern medicine.

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