Cas no 66497-42-5 (3-hydroxy-6-methylpyridine-2-carbaldehyde)

3-Hydroxy-6-methylpyridine-2-carbaldehyde is a heterocyclic organic compound featuring both hydroxyl and aldehyde functional groups on a pyridine backbone. This structure imparts reactivity suitable for use as an intermediate in pharmaceutical and agrochemical synthesis. The presence of the aldehyde group allows for further functionalization via condensation or nucleophilic addition reactions, while the hydroxyl group enhances solubility and offers additional sites for modification. Its methyl substitution at the 6-position contributes to steric and electronic effects, influencing regioselectivity in subsequent reactions. The compound is valued for its versatility in constructing complex molecular frameworks, particularly in the development of bioactive molecules and coordination chemistry applications.
3-hydroxy-6-methylpyridine-2-carbaldehyde structure
66497-42-5 structure
Product Name:3-hydroxy-6-methylpyridine-2-carbaldehyde
CAS No:66497-42-5
MF:C7H7NO2
MW:137.135981798172
MDL:MFCD11044356
CID:502273
PubChem ID:12421986
Update Time:2025-05-19

3-hydroxy-6-methylpyridine-2-carbaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-hydroxy-6-methyl-2-Pyridinecarboxaldehyde
    • 2-Pyridinecarboxaldehyde,3-hydroxy-6-methyl-
    • 3-hydroxy-6-methyl-2-pyridinecarbaldehyde(SALTDATA: FREE)
    • 3-hydroxy-6-methylpyridine-2-carbaldehyde
    • 2-formyl-3-hydroxy-6-methylpyridine
    • 3-hydroxy-6-methyl-2-pyridinecarbaldehyde
    • 3-hydroxy-6-methyl-2-pyridinecarboxyaldehyde
    • 3-hydroxy-6-methyl-pyridine-2-carbaldehyde
    • 3-Hydroxy-6-methylpyridine-2-carboxaldehyde
    • DTXSID30497500
    • EN300-69366
    • CS-0130306
    • 3-Hydroxy-6-methylpicolinaldehyde
    • A914224
    • SCHEMBL1390456
    • SY185839
    • AB62933
    • AS-65772
    • Z1104852896
    • 3-hydroxy-6-methyl-2-pyridine aldehyde
    • FT-0748808
    • AKOS005264543
    • RDQQJPSVWVFAJK-UHFFFAOYSA-N
    • 3-Hydroxy-6-methyl-2-pyridinecarbaldehyde, 95%
    • 2-Pyridinecarboxaldehyde, 3-hydroxy-6-methyl-
    • W11337
    • 66497-42-5
    • 3-Hydroxy-6-methyl-2-pyridine carbaldehyde
    • MFCD11044356
    • DB-082224
    • MDL: MFCD11044356
    • Inchi: 1S/C7H7NO2/c1-5-2-3-7(10)6(4-9)8-5/h2-4,10H,1H3
    • InChI Key: RDQQJPSVWVFAJK-UHFFFAOYSA-N
    • SMILES: OC1C=CC(C)=NC=1C=O

Computed Properties

  • Exact Mass: 137.04800
  • Monoisotopic Mass: 137.047678466g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 127
  • 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: 1.2
  • Topological Polar Surface Area: 50.2?2

Experimental Properties

  • Density: 1.258
  • Boiling Point: 283.596°C at 760 mmHg
  • Flash Point: 125.315°C
  • Refractive Index: 1.61
  • PSA: 50.19000
  • LogP: 0.90810

3-hydroxy-6-methylpyridine-2-carbaldehyde 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%

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3-hydroxy-6-methylpyridine-2-carbaldehyde Related Literature

Additional information on 3-hydroxy-6-methylpyridine-2-carbaldehyde

Comprehensive Overview of 3-hydroxy-6-methylpyridine-2-carbaldehyde (CAS No. 66497-42-5): Properties, Applications, and Innovations

3-hydroxy-6-methylpyridine-2-carbaldehyde (CAS No. 66497-42-5) is a versatile organic compound with a pyridine backbone, widely recognized for its unique chemical properties and broad applicability in pharmaceuticals, agrochemicals, and material science. This heterocyclic aldehyde features a hydroxyl group at the 3-position and a methyl group at the 6-position, making it a valuable intermediate in synthetic chemistry. Its molecular formula, C7H7NO2, and structural specificity have garnered significant attention from researchers exploring bioactive molecules and catalysis.

In recent years, the demand for 3-hydroxy-6-methylpyridine-2-carbaldehyde has surged due to its role in developing antioxidant agents and metal-chelating ligands. A growing trend in green chemistry has further highlighted its potential as a sustainable building block for biodegradable materials. Users frequently search for its synthesis methods, solubility data, and safety profiles, reflecting its relevance in both academic and industrial settings. Notably, its CAS No. 66497-42-5 serves as a critical identifier in regulatory and procurement databases.

The compound’s pharmaceutical applications are particularly noteworthy. Studies suggest its derivatives exhibit neuroprotective effects, aligning with the rising interest in neurodegenerative disease research. Additionally, its chelating properties are exploited in designing fluorescence probes for environmental monitoring, a hot topic in pollution detection. Researchers also explore its use in coordination polymers, addressing queries about advanced material design.

From a commercial perspective, 3-hydroxy-6-methylpyridine-2-carbaldehyde is often discussed alongside cost-effective synthesis routes and scalability challenges. Manufacturers emphasize its high purity grades (>98%) to meet the stringent requirements of drug formulation and catalysis. Analytical techniques like HPLC and NMR spectroscopy are routinely employed to verify its quality, a detail frequently sought by quality control professionals.

Innovations in catalytic oxidation have further expanded its utility. For instance, its incorporation into asymmetric synthesis protocols addresses the demand for chiral intermediates in API production. Environmental scientists also investigate its degradation pathways, responding to public concerns about chemical persistence in ecosystems. These interdisciplinary applications underscore its adaptability to emerging technologies.

In summary, 3-hydroxy-6-methylpyridine-2-carbaldehyde (CAS No. 66497-42-5) stands at the intersection of synthetic chemistry, pharmaceutical innovation, and environmental science. Its multifaceted roles and evolving applications make it a compound of enduring significance, poised to address future challenges in healthcare and sustainable industry.

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