Cas no 85553-55-5 (4-3-(Hydroxymethyl)phenylpyridine)

4-3-(Hydroxymethyl)phenylpyridine is a versatile organic compound featuring a hydroxymethylphenyl group attached to a pyridine ring. This structure imparts unique reactivity, making it valuable as an intermediate in pharmaceutical synthesis and material science applications. The hydroxymethyl group enhances solubility and provides a reactive site for further functionalization, while the pyridine moiety contributes to coordination properties, useful in ligand design. Its balanced hydrophilicity and lipophilicity improve processability in organic reactions. The compound’s stability under standard conditions ensures reliable handling and storage. Its structural motifs are particularly relevant in developing bioactive molecules and advanced polymers, offering flexibility for tailored modifications in research and industrial settings.
4-3-(Hydroxymethyl)phenylpyridine structure
85553-55-5 structure
Product Name:4-3-(Hydroxymethyl)phenylpyridine
CAS No:85553-55-5
MF:C12H11NO
MW:185.221843004227
CID:719989
PubChem ID:2795564
Update Time:2025-07-01

4-3-(Hydroxymethyl)phenylpyridine Chemical and Physical Properties

Names and Identifiers

    • (3-(Pyridin-4-yl)phenyl)methanol
    • (3-Pyrid-4-ylphenyl)methanol
    • (3-pyridin-4-ylphenyl)methanol
    • Benzenemethanol,3-(4-pyridinyl)-
    • 3-(Pyridin-4-yl)benzyl alcohol
    • 4-[3-(Hydroxymethyl)phenyl]pyridine
    • 4-[3-(Hydroxymethyl)phenyl]pyridine 97%
    • (3-PYRIDIN-4YLPHENYL)METHANOL
    • 4-(3-HYDROXYMETHYLPHENYL)PYRIDINE
    • [3-(Pyridin-4-yl)phenyl]methanol 97%
    • 4-[3-(Hydroxymethyl)phenyl]pyridine, 3-(Pyridin-4-yl)benzyl alcohol
    • [3-(Pyridin-4-yl)phenyl]methanol97%
    • Benzenemethanol, 3-(4-pyridinyl)-
    • (3-pyrid-4-ylphenyl)methanol, AldrichCPR
    • CHEMBL4211034
    • 85553-55-5
    • MS-22260
    • SCHEMBL12641314
    • MFCD06659083
    • [3-(pyridin-4-yl)phenyl]methanol
    • CS-0330889
    • J-501087
    • BDBM50455613
    • SB54420
    • DTXSID00383784
    • AKOS006345972
    • 4-3-(Hydroxymethyl)phenylpyridine
    • MDL: MFCD06659083
    • Inchi: 1S/C12H11NO/c14-9-10-2-1-3-12(8-10)11-4-6-13-7-5-11/h1-8,14H,9H2
    • InChI Key: ZORHPGKUTIFODF-UHFFFAOYSA-N
    • SMILES: C1(CO)=CC=CC(C2C=CN=CC=2)=C1

Computed Properties

  • Exact Mass: 185.08400
  • Monoisotopic Mass: 185.084063974g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 166
  • 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: 1.7
  • Topological Polar Surface Area: 33.1?2

Experimental Properties

  • Density: 1.145
  • Boiling Point: 344.7°C at 760 mmHg
  • Flash Point: 162.3°C
  • Refractive Index: 1.6
  • PSA: 33.12000
  • LogP: 2.24090

4-3-(Hydroxymethyl)phenylpyridine Security Information

  • Hazard Statement: Harmful
  • Hazard Category Code: 22
  • Hazardous Material Identification: Xn

4-3-(Hydroxymethyl)phenylpyridine 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%

4-3-(Hydroxymethyl)phenylpyridine Pricemore >>

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Additional information on 4-3-(Hydroxymethyl)phenylpyridine

4-3-(Hydroxymethyl)phenylpyridine (CAS No. 85553-55-5)

4-3-(Hydroxymethyl)phenylpyridine, also known by its CAS registry number 85553-55-5, is a compound of significant interest in the fields of organic chemistry and materials science. This compound, with its unique structural features, has been the subject of extensive research in recent years. Its structure comprises a pyridine ring substituted at the 4-position with a hydroxymethyl group attached to a phenyl ring. This configuration imparts distinctive electronic and steric properties, making it a valuable molecule for various applications.

The synthesis of 4-3-(Hydroxymethyl)phenylpyridine typically involves multi-step organic reactions, often utilizing coupling reactions or substitution mechanisms. Recent advancements in catalytic methods have enabled more efficient and selective syntheses, reducing production costs and enhancing purity. The compound's ability to act as both an electron donor and acceptor makes it particularly useful in electronic materials, such as organic semiconductors and light-emitting diodes (LEDs). Researchers have explored its potential in creating flexible electronics due to its excellent charge transport properties.

In the realm of pharmacology, 4-3-(Hydroxymethyl)phenylpyridine has shown promise as a lead compound for drug development. Its hydroxymethyl group facilitates hydrogen bonding, which is crucial for bioavailability and target binding affinity. Studies have demonstrated its potential as an inhibitor of certain enzymes involved in metabolic disorders, offering new avenues for therapeutic interventions. The phenylpyridine moiety also exhibits anti-inflammatory properties, making it a candidate for anti-inflammatory drug design.

The environmental impact of 4-3-(Hydroxymethyl)phenylpyridine has also been a focus of recent research. Its biodegradability and toxicity profiles are being evaluated to ensure sustainable use in industrial applications. Green chemistry approaches are being employed to minimize waste and energy consumption during its synthesis, aligning with global efforts to promote eco-friendly chemical processes.

In conclusion, 4-3-(Hydroxymethyl)phenylpyridine (CAS No. 85553-55-5) stands out as a versatile compound with diverse applications across multiple disciplines. Its unique chemical structure, combined with cutting-edge synthetic methods and functional properties, positions it as a key player in advancing modern materials science and pharmacology.

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