Cas no 351410-62-3 (5-fluoro-2-methoxypyridine-3-carbaldehyde)

5-Fluoro-2-methoxypyridine-3-carbaldehyde is a versatile heterocyclic building block used in organic synthesis and pharmaceutical research. Its structure features a fluorine substituent at the 5-position and a methoxy group at the 2-position, enhancing its reactivity and selectivity in cross-coupling reactions, nucleophilic additions, and condensation processes. The aldehyde functional group at the 3-position makes it a valuable intermediate for constructing more complex molecules, such as ligands, agrochemicals, and active pharmaceutical ingredients (APIs). The electron-withdrawing fluorine atom improves metabolic stability in drug development, while the methoxy group can influence regioselectivity. This compound is particularly useful in medicinal chemistry for designing fluorinated analogs with optimized pharmacokinetic properties.
5-fluoro-2-methoxypyridine-3-carbaldehyde structure
351410-62-3 structure
Product Name:5-fluoro-2-methoxypyridine-3-carbaldehyde
CAS No:351410-62-3
MF:C7H6FNO2
MW:155.126445293427
MDL:MFCD04972398
CID:67797
PubChem ID:22678323
Update Time:2025-05-21

5-fluoro-2-methoxypyridine-3-carbaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-Fluoro-2-methoxy-6-methylpyridine
    • 5-fluoro-2-methoxy-3-pyridinecarboxaldehyde
    • 5-Fluoro-2-methoxynicotinaldehyde
    • 5-fluoro-2-methoxypyridine-3-carbaldehyde
    • 5-Fluoro-2-methoxypyridine-3-carboxaldehyde
    • 2-Methoxy-5-fluoropyridine-3-carbaldehyde
    • 5-fluoro-2-methoxy-pyridine-3-carbaldehyde
    • 5-Fluoro-3-formyl-2-methoxypyridine
    • 3-PYRIDINECARBOXALDEHYDE, 5-FLUORO-2-METHOXY-
    • 5-Fluoro-2-methoxy-3-pyridine carboxaldehyde
    • 3-Pyridinecarboxaldehyde,5-fluoro-2-methoxy-
    • PubChem16100
    • YAGPZRLCMRMSFP-UHFFFAOYSA-N
    • BCP2460
    • MFCD04972398
    • BCP24605
    • AB20973
    • AC-33363
    • AM62421
    • J-517516
    • A6170
    • SY065663
    • AKOS005063679
    • 351410-62-3
    • DTXSID80627552
    • SCHEMBL1116679
    • FT-0648109
    • CS-0062015
    • DS-12753
    • 5-fluoro-2-methoxynicotinaldehyde, AldrichCPR
    • Pyridine5-fluoro-2-methoxy-3-carboxaldehyde
    • DB-025156
    • MDL: MFCD04972398
    • Inchi: 1S/C7H6FNO2/c1-11-7-5(4-10)2-6(8)3-9-7/h2-4H,1H3
    • InChI Key: YAGPZRLCMRMSFP-UHFFFAOYSA-N
    • SMILES: FC1=CN=C(C(C=O)=C1)OC

Computed Properties

  • Exact Mass: 155.03800
  • Monoisotopic Mass: 155.038
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 142
  • 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
  • Topological Polar Surface Area: 39.2
  • XLogP3: 0.7

Experimental Properties

  • Color/Form: No data available
  • Density: 1.3
  • Melting Point: No data available
  • Boiling Point: 233.2 oC at 760 mmHg
  • Flash Point: 94.8 oC
  • Refractive Index: 1.52
  • PSA: 39.19000
  • LogP: 1.04180
  • Sensitiveness: Air & Moisture Sensitive

5-fluoro-2-methoxypyridine-3-carbaldehyde Security Information

5-fluoro-2-methoxypyridine-3-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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Additional information on 5-fluoro-2-methoxypyridine-3-carbaldehyde

5-Fluoro-2-methoxypyridine-3-carbaldehyde: A Comprehensive Overview

5-fluoro-2-methoxypyridine-3-carbaldehyde (CAS No. 351410-62-3) is a chemically synthesized compound that has garnered significant attention in the fields of organic chemistry, pharmacology, and materials science. This compound is characterized by its unique structure, which includes a pyridine ring substituted with a fluoro group at the 5-position, a methoxy group at the 2-position, and a formyl (carbaldehyde) group at the 3-position. The combination of these substituents imparts distinctive electronic and steric properties to the molecule, making it a valuable compound for various applications.

The synthesis of 5-fluoro-2-methoxypyridine-3-carbaldehyde involves a series of well-established organic reactions. Typically, the synthesis begins with the preparation of a pyridine derivative, followed by selective substitution reactions to introduce the fluoro and methoxy groups. The final step involves the introduction of the aldehyde group through oxidation or direct alkylation methods. Recent advancements in catalytic systems and green chemistry have enabled more efficient and environmentally friendly routes for its synthesis, which aligns with current trends in sustainable chemical manufacturing.

One of the most notable applications of 5-fluoro-2-methoxypyridine-3-carbaldehyde is in drug discovery. The compound serves as a valuable building block for constructing bioactive molecules with potential therapeutic applications. For instance, studies have shown that this compound exhibits moderate inhibitory activity against certain enzymes involved in cancer progression. Additionally, its ability to act as a ligand in metalloenzyme models has opened new avenues for exploring its role in catalytic processes relevant to drug metabolism.

In materials science, 5-fluoro-2-methoxypyridine-3-carbaldehyde has been investigated for its potential as a precursor in the synthesis of advanced materials such as coordination polymers and metal-organic frameworks (MOFs). The aldehyde group facilitates coordination with metal ions, while the electron-withdrawing fluoro and methoxy groups influence the overall electronic properties of the resulting materials. Recent research has demonstrated that MOFs derived from this compound exhibit exceptional gas adsorption capabilities, making them promising candidates for environmental remediation applications.

From an analytical standpoint, 5-fluoro-2-methoxypyridine-3-carbaldehyde has been extensively studied using modern spectroscopic techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. These studies have provided critical insights into its molecular structure, stability, and reactivity under various conditions. Furthermore, computational chemistry approaches have been employed to predict its electronic properties and reactivity trends, which have been validated through experimental studies.

Recent breakthroughs in medicinal chemistry have highlighted the potential of 5-fluoro-2-methoxypyridine-3-carbaldehyde as a lead compound for developing novel antibiotics. Its unique structure allows for interactions with bacterial enzymes that are critical for cell wall synthesis, making it a promising candidate for combating antibiotic-resistant pathogens. Collaborative efforts between academic institutions and pharmaceutical companies are currently underway to explore its therapeutic potential further.

In conclusion, 5-fluoro-2-methoxypyridine-3-carbaldehyde (CAS No. 351410-62-3) stands out as a versatile compound with diverse applications across multiple scientific disciplines. Its distinctive chemical properties, coupled with advancements in synthetic methodologies and analytical techniques, continue to drive innovative research into its potential uses. As ongoing studies uncover new insights into its biological and materials-related properties, this compound is poised to play an increasingly important role in advancing scientific knowledge and technological applications.

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