Cas no 1849-54-3 (3-Hydroxypyridine-4-carboxaldehyde)

3-Hydroxypyridine-4-carboxaldehyde is a versatile heterocyclic compound featuring both hydroxyl and aldehyde functional groups on a pyridine scaffold. This structure makes it a valuable intermediate in organic synthesis, particularly for the preparation of pharmaceuticals, agrochemicals, and coordination complexes. The aldehyde group enables condensation reactions, while the hydroxyl group offers additional reactivity for derivatization or metal chelation. Its well-defined reactivity profile and stability under standard conditions facilitate precise modifications in multi-step syntheses. The compound is particularly useful in the development of bioactive molecules and ligands for catalytic systems. High purity grades are available to ensure consistent performance in research and industrial applications.
3-Hydroxypyridine-4-carboxaldehyde structure
1849-54-3 structure
Product Name:3-Hydroxypyridine-4-carboxaldehyde
CAS No:1849-54-3
MF:C6H5NO2
MW:123.109401464462
MDL:MFCD01318565
CID:42083
PubChem ID:192747
Update Time:2025-11-07

3-Hydroxypyridine-4-carboxaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-Hydroxypyridine-4-carboxaldehyde
    • 3-hydroxy-4-pyridinecarboxaldehyde
    • 3-Hydroxyisonicotinaldehyde
    • 3-HYDROXY-PYRIDINE-4-CARBALDEHYDE
    • 3-hydroxypyridine-4-carbaldehyde
    • 3-Hydroxy-4-formylpyridine
    • 3-hydroxy-4-pyridinaldehyde
    • 4-Formyl-3-hydroxypyridine
    • 3-HYDROXY-ISONICOTINALDEHYDE
    • 3-Hydroxypyridin-4-carbaldehyde
    • 4-Pyridinecarboxaldehyde, 3-hydroxy-
    • 4-Formyl-3-hydroxypyridine 3-Hydroxy-isonicotinaldehyde
    • 3-hydroxypyridine-4-aldehyde
    • 3-Hydroxy-4-pyridinecarbaldehyde
    • NVLPDIRQWJSXLZ-UHFFFAOYSA-N
    • EBD39347
    • KS-0
    • SY014482
    • 55780-71-7
    • AKOS002669574
    • AB08714
    • AM807039
    • MFCD01318565
    • 1849-54-3
    • SCHEMBL1043345
    • CS-W005203
    • DS-10463
    • J-512659
    • FT-0650299
    • TETRA-N-HEXYLAMMONIUMIODIDE
    • A15330
    • DTXSID50171673
    • pyridine, 4-formyl-3-hydroxy-
    • DB-017554
    • DTXCID4094164
    • MDL: MFCD01318565
    • Inchi: 1S/C6H5NO2/c8-4-5-1-2-7-3-6(5)9/h1-4,9H
    • InChI Key: NVLPDIRQWJSXLZ-UHFFFAOYSA-N
    • SMILES: OC1C=NC=CC=1C=O

Computed Properties

  • Exact Mass: 123.03200
  • Monoisotopic Mass: 123.032
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 105
  • 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: 0.5
  • Topological Polar Surface Area: 50.2

Experimental Properties

  • Density: 1.327
  • Boiling Point: 323.8℃ at 760 mmHg
  • Flash Point: 149.7 °C
  • Refractive Index: 1.629
  • PSA: 50.19000
  • LogP: 0.59970

3-Hydroxypyridine-4-carboxaldehyde Security Information

3-Hydroxypyridine-4-carboxaldehyde 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-Hydroxypyridine-4-carboxaldehyde Pricemore >>

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3-Hydroxypyridine-4-carboxaldehyde Related Literature

Additional information on 3-Hydroxypyridine-4-carboxaldehyde

3-Hydroxypyridine-4-carboxaldehyde (CAS No. 1849-54-3): An Overview of Its Properties, Applications, and Recent Research

3-Hydroxypyridine-4-carboxaldehyde (CAS No. 1849-54-3) is a versatile organic compound that has garnered significant attention in the fields of chemistry, biology, and pharmaceuticals due to its unique structural features and potential applications. This compound is characterized by a pyridine ring with a hydroxyl group at the 3-position and an aldehyde group at the 4-position. The combination of these functional groups imparts 3-Hydroxypyridine-4-carboxaldehyde with a range of chemical properties that make it valuable in various scientific and industrial contexts.

The chemical structure of 3-Hydroxypyridine-4-carboxaldehyde (C6H5NO2) is particularly noteworthy for its aromaticity and the presence of both electron-donating (hydroxyl) and electron-withdrawing (aldehyde) groups. These features contribute to its reactivity and stability, making it an attractive starting material for synthetic chemistry. The compound can be synthesized through various methods, including the condensation of pyridine derivatives with appropriate carbonyl compounds, followed by oxidation and hydroxylation steps.

In the realm of medicinal chemistry, 3-Hydroxypyridine-4-carboxaldehyde has been explored for its potential therapeutic applications. Recent studies have highlighted its role as a precursor in the synthesis of bioactive molecules, particularly those with anti-inflammatory and antioxidant properties. For instance, a study published in the Journal of Medicinal Chemistry in 2022 reported the synthesis of novel pyridine derivatives from 3-Hydroxypyridine-4-carboxaldehyde, which exhibited potent anti-inflammatory activity in vitro and in vivo models.

The aldehyde group in 3-Hydroxypyridine-4-carboxaldehyde makes it a valuable intermediate in the preparation of Schiff bases, which are known for their biological activities. Schiff bases derived from 3-Hydroxypyridine-4-carboxaldehyde have been investigated for their antimicrobial, antifungal, and anticancer properties. A 2021 study in the European Journal of Medicinal Chemistry demonstrated that certain Schiff bases synthesized from 3-Hydroxypyridine-4-carboxaldehyde showed significant cytotoxic activity against various cancer cell lines.

Beyond its medicinal applications, 3-Hydroxypyridine-4-carboxaldehyde has also found use in analytical chemistry. Its unique spectral properties make it suitable for various analytical techniques, including UV-Vis spectroscopy and high-performance liquid chromatography (HPLC). These methods are crucial for the quantitative analysis of 3-Hydroxypyridine-4-carboxaldehyde in complex mixtures, which is essential for quality control in pharmaceutical and chemical industries.

In environmental chemistry, 3-Hydroxypyridine-4-carboxaldehyde has been studied for its potential as a biomarker for environmental pollutants. Research published in Environmental Science & Technology in 2020 indicated that 3-Hydroxypyridine-4-carboxaldehyde-derived compounds can be used to monitor the presence of certain pollutants in water and soil samples. This application highlights the compound's versatility and its importance in environmental monitoring and remediation efforts.

The safety profile of 3-Hydroxypyridine-4-carboxaldehyde is another critical aspect that has been extensively studied. While it is generally considered safe for laboratory use when proper handling protocols are followed, it is important to note that exposure to high concentrations or prolonged exposure may pose health risks. Therefore, appropriate personal protective equipment (PPE) and ventilation systems should be used when handling this compound.

In conclusion, 3-Hydroxypyridine-4-carboxaldehyde (CAS No. 1849-54-3) is a multifaceted compound with a wide range of applications in chemistry, biology, and pharmaceuticals. Its unique chemical structure and reactivity make it an invaluable intermediate in synthetic chemistry, while its biological activities offer promising avenues for drug discovery and development. Ongoing research continues to uncover new possibilities for this compound, further solidifying its importance in various scientific disciplines.

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