Cas no 85259-48-9 (6-Propoxy-3-pyridinecarboxaldehyde)

6-Propoxy-3-pyridinecarboxaldehyde is a versatile pyridine derivative characterized by its aldehyde functional group and propoxy substitution at the 6-position. This compound serves as a valuable intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its reactive aldehyde group enables facile derivatization, while the propoxy moiety enhances solubility and influences electronic properties, making it useful in cross-coupling reactions and heterocyclic scaffold construction. The compound exhibits stability under standard handling conditions and is compatible with a range of synthetic methodologies. Its structural features make it a practical choice for researchers developing novel bioactive molecules or functional materials.
6-Propoxy-3-pyridinecarboxaldehyde structure
85259-48-9 structure
Product Name:6-Propoxy-3-pyridinecarboxaldehyde
CAS No:85259-48-9
MF:C9H11NO2
MW:165.189142465591
CID:1835725
PubChem ID:79002144
Update Time:2025-10-23

6-Propoxy-3-pyridinecarboxaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-Pyridinecarboxaldehyde, 6-propoxy-
    • DB-207806
    • AKOS017515584
    • 2-propoxy-5-pyridinecarbaldehyde
    • 85259-48-9
    • SCHEMBL20489821
    • 6-Propoxy-3-pyridinecarboxaldehyde
    • 6-propoxypyridine-3-carbaldehyde
    • Inchi: 1S/C9H11NO2/c1-2-5-12-9-4-3-8(7-11)6-10-9/h3-4,6-7H,2,5H2,1H3
    • InChI Key: MFIYHHBEGFWQNX-UHFFFAOYSA-N
    • SMILES: O(C1C=CC(C=O)=CN=1)CCC

Computed Properties

  • Exact Mass: 165.078978594g/mol
  • Monoisotopic Mass: 165.078978594g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 4
  • Complexity: 139
  • 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: 1.5
  • Topological Polar Surface Area: 39.2?2

6-Propoxy-3-pyridinecarboxaldehyde Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
P993728-10mg
6-Propoxy-3-pyridinecarboxaldehyde
85259-48-9
10mg
$ 50.00 2022-06-03
TRC
P993728-50mg
6-Propoxy-3-pyridinecarboxaldehyde
85259-48-9
50mg
$ 160.00 2022-06-03
TRC
P993728-100mg
6-Propoxy-3-pyridinecarboxaldehyde
85259-48-9
100mg
$ 230.00 2022-06-03

Additional information on 6-Propoxy-3-pyridinecarboxaldehyde

6-Propoxy-3-Pyridinecarboxaldehyde (CAS No. 85259-48-9): A Comprehensive Overview

6-Propoxy-3-pyridinecarboxaldehyde (CAS No. 85259-48-9) is a versatile organic compound that has garnered significant attention in the fields of chemical synthesis, medicinal chemistry, and materials science. This compound, also known as 6-propoxypyridine-3-carbaldehyde, is characterized by its unique structural features, which include a pyridine ring and a propoxy substituent. These characteristics make it an attractive building block for a wide range of applications, from the synthesis of complex organic molecules to the development of novel pharmaceuticals.

The molecular formula of 6-Propoxy-3-pyridinecarboxaldehyde is C10H11NO2, and its molecular weight is 177.20 g/mol. The compound is a colorless to pale yellow liquid at room temperature and is soluble in common organic solvents such as ethanol, methanol, and dichloromethane. Its physical and chemical properties have been extensively studied, providing a solid foundation for its use in various scientific and industrial processes.

In the realm of chemical synthesis, 6-Propoxy-3-pyridinecarboxaldehyde serves as a valuable intermediate in the preparation of more complex molecules. Its reactivity and functional group versatility allow it to participate in a variety of reactions, including condensation, reduction, and oxidation processes. Recent research has highlighted its utility in the synthesis of heterocyclic compounds, which are crucial components in many pharmaceuticals and agrochemicals.

The medicinal chemistry community has shown particular interest in 6-Propoxy-3-pyridinecarboxaldehyde due to its potential as a lead compound for drug discovery. Pyridine derivatives are known for their biological activities, including anti-inflammatory, antiviral, and anticancer properties. Studies have demonstrated that compounds derived from 6-Propoxy-3-pyridinecarboxaldehyde exhibit promising pharmacological effects, making them candidates for further development into therapeutic agents.

In the context of materials science, 6-Propoxy-3-pyridinecarboxaldehyde has been explored for its potential applications in the development of functional materials. For instance, it can be used as a building block for the synthesis of luminescent materials and polymers with unique optical properties. These materials have potential applications in areas such as organic light-emitting diodes (OLEDs) and sensors.

The environmental impact of 6-Propoxy-3-pyridinecarboxaldehyde has also been a subject of study. Research indicates that while the compound itself is not considered highly toxic or environmentally hazardous, proper handling and disposal practices are essential to minimize any potential risks. Environmental scientists continue to monitor the fate and behavior of this compound in various ecosystems to ensure its safe use.

In conclusion, 6-Propoxy-3-pyridinecarboxaldehyde (CAS No. 85259-48-9) is a multifaceted compound with a wide range of applications across multiple scientific disciplines. Its unique structural features and versatile reactivity make it an invaluable tool for researchers and industry professionals alike. As ongoing research continues to uncover new possibilities for this compound, its importance in the fields of chemical synthesis, medicinal chemistry, and materials science is likely to grow even further.

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