Cas no 193481-63-9 (3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro-)

3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro-, is a fluorinated pyridine derivative featuring a dimethylamino substituent at the 6-position and an aldehyde functional group at the 3-position. This compound is of interest in synthetic organic chemistry due to its versatile reactivity, particularly in the formation of heterocyclic structures and as a building block for pharmaceuticals or agrochemicals. The fluorine atom enhances electrophilic properties, while the dimethylamino group contributes to electron-donating effects, influencing regioselectivity in reactions. Its well-defined structure and functional group compatibility make it valuable for designing complex molecules, with potential applications in medicinal chemistry and material science.
3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro- structure
193481-63-9 structure
Product Name:3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro-
CAS No:193481-63-9
MF:C8H9FN2O
MW:168.168265104294
MDL:MFCD23713090
CID:3860198
PubChem ID:10607190
Update Time:2025-11-06

3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro- Chemical and Physical Properties

Names and Identifiers

    • 3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro-
    • 2-Fluoro-6-dimethylaminopiridine-3- carbaldehyde
    • MFCD23713090
    • E92686
    • 6-(dimethylamino)-2-fluoronicotinaldehyde
    • 2-Fluoro-6-dimethylaminopiridine-3-carbaldehyde
    • 2-Fluoro-6-dimethylaminopyridine-3-carbaldehyde
    • AKOS024263385
    • CS-0195362
    • 6-(DIMETHYLAMINO)-2-FLUOROPYRIDINE-3-CARBALDEHYDE
    • 193481-63-9
    • MDL: MFCD23713090
    • Inchi: 1S/C8H9FN2O/c1-11(2)7-4-3-6(5-12)8(9)10-7/h3-5H,1-2H3
    • InChI Key: AJCPLOXHJUASRT-UHFFFAOYSA-N
    • SMILES: C1(F)=NC(N(C)C)=CC=C1C=O

Computed Properties

  • Exact Mass: 168.06989108Da
  • Monoisotopic Mass: 168.06989108Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 163
  • 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: 33.2?2

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Additional information on 3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro-

3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro-

The compound 3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro- (CAS No: 193481-63-9) is a highly specialized organic molecule with significant applications in various fields of chemistry and materials science. This compound belongs to the class of pyridine derivatives, which are known for their unique electronic properties and versatile reactivity. The presence of the dimethylamino group and the fluoro substituent introduces additional complexity to its structure, making it a valuable compound for research and industrial applications.

Recent studies have highlighted the importance of pyridine derivatives in the development of advanced materials, particularly in the field of electronics and optoelectronics. The dimethylamino group attached to the pyridine ring enhances the molecule's electron-donating ability, which is crucial for applications such as light-emitting diodes (LEDs) and organic photovoltaics (OPVs). Additionally, the fluoro substituent contributes to the molecule's stability and solubility, making it suitable for use in high-performance materials.

In terms of synthesis, 3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro- can be prepared through a variety of methods, including nucleophilic aromatic substitution and coupling reactions. These methods allow for precise control over the substitution pattern on the pyridine ring, enabling the creation of tailored structures with specific properties. Recent advancements in catalytic systems have further improved the efficiency and selectivity of these reactions, making them more accessible for large-scale production.

The compound's applications extend beyond materials science into pharmaceuticals and agrochemicals. Its unique electronic properties make it a promising candidate for use as a ligand in metalloenzyme mimics and catalysts. Furthermore, its ability to form stable complexes with metal ions has led to its exploration in drug delivery systems and sensing technologies.

From an environmental perspective, 3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro- has been studied for its biodegradability and eco-friendly synthesis pathways. Researchers have developed green chemistry approaches to synthesize this compound using renewable feedstocks and energy-efficient processes. These efforts align with global sustainability goals and highlight the compound's potential for use in environmentally responsible industries.

In conclusion, 3-Pyridinecarboxaldehyde, 6-(dimethylamino)-2-fluoro- (CAS No: 193481-63-9) is a multifaceted compound with a wide range of applications across various scientific disciplines. Its unique structure and functional groups make it a valuable tool for researchers and industry professionals alike. As new discoveries continue to emerge, this compound is poised to play an even more significant role in shaping future technologies.

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