Cas no 1211584-76-7 (5-Amino-2-methoxy-3-(trifluoromethyl)pyridine)

5-Amino-2-methoxy-3-(trifluoromethyl)pyridine is a fluorinated pyridine derivative with significant utility in pharmaceutical and agrochemical synthesis. Its trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable for designing bioactive compounds. The amino and methoxy substituents provide versatile sites for further functionalization, enabling tailored modifications in drug discovery and material science applications. This compound exhibits high purity and stability under standard conditions, ensuring reliable performance in synthetic workflows. Its unique structure is particularly advantageous in the development of fluorinated heterocycles, where electronic and steric properties are critical. Suitable for research and industrial use, it serves as a key intermediate in advanced organic synthesis.
5-Amino-2-methoxy-3-(trifluoromethyl)pyridine structure
1211584-76-7 structure
Product Name:5-Amino-2-methoxy-3-(trifluoromethyl)pyridine
CAS No:1211584-76-7
MF:C7H7F3N2O
MW:192.138491868973
MDL:MFCD17168449
CID:1056632
PubChem ID:66600485
Update Time:2025-07-23

5-Amino-2-methoxy-3-(trifluoromethyl)pyridine Chemical and Physical Properties

Names and Identifiers

    • 6-Methoxy-5-(trifluoromethyl)pyridin-3-amine
    • 2-methoxy-3-(trifluoromethyl)pyridine
    • 3-?Pyridinamine, 6-?methoxy-?5-?(trifluoromethyl)?-
    • 5-Amino-2-methoxy-3-(trifluoromethyl)pyridine
    • 6-methoxy-5-(trifluoromethyl)-3-Pyridinamine
    • AHFNQSHZCUHVFS-UHFFFAOYSA-N
    • 6320AJ
    • TRA0037016
    • AB71712
    • SY014645
    • AK147213
    • 3-Pyridinamine, 6-methoxy-5-(trifluoromethyl)-
    • 5-(TRIFLUOROMETHYL)-6-METHOXYPYRIDIN-3-AMINE
    • 2-?Propenoic acid, 3-?(1H-?pyrrol-?
    • AKOS022187325
    • 1211584-76-7
    • MFCD17168449
    • DS-8703
    • EN300-1295625
    • CS-W022508
    • A891873
    • SCHEMBL116558
    • MDL: MFCD17168449
    • Inchi: 1S/C7H7F3N2O/c1-13-6-5(7(8,9)10)2-4(11)3-12-6/h2-3H,11H2,1H3
    • InChI Key: AHFNQSHZCUHVFS-UHFFFAOYSA-N
    • SMILES: FC(C1C(=NC=C(C=1)N)OC)(F)F

Computed Properties

  • Exact Mass: 192.05100
  • Monoisotopic Mass: 192.05104734g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 174
  • 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: 48.1
  • XLogP3: 1.4

Experimental Properties

  • Density: 1.348±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 272.4±40.0 oC (760 Torr),
  • Flash Point: 118.5±27.3 oC,
  • Solubility: Slightly soluble (4 g/l) (25 o C),
  • PSA: 48.14000
  • LogP: 2.27240

5-Amino-2-methoxy-3-(trifluoromethyl)pyridine Security Information

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Additional information on 5-Amino-2-methoxy-3-(trifluoromethyl)pyridine

Research Brief on 5-Amino-2-methoxy-3-(trifluoromethyl)pyridine (CAS: 1211584-76-7): Recent Advances and Applications

5-Amino-2-methoxy-3-(trifluoromethyl)pyridine (CAS: 1211584-76-7) is a fluorinated pyridine derivative that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural and electronic properties. This compound serves as a versatile building block in medicinal chemistry, particularly in the synthesis of novel drug candidates targeting various diseases. Recent studies have explored its applications in kinase inhibitors, agrochemicals, and other biologically active molecules, leveraging its trifluoromethyl group for enhanced metabolic stability and binding affinity.

In a 2023 study published in the Journal of Medicinal Chemistry, researchers utilized 5-Amino-2-methoxy-3-(trifluoromethyl)pyridine as a key intermediate in the development of selective JAK2 inhibitors. The trifluoromethyl group was found to significantly improve the pharmacokinetic profile of the inhibitors, demonstrating enhanced oral bioavailability and reduced off-target effects. The study highlighted the compound's role in optimizing drug-like properties, making it a valuable scaffold for kinase-targeted therapies.

Another notable application of this compound was reported in the field of agrochemicals. A 2022 study in Pest Management Science demonstrated its incorporation into novel fungicides, where the electron-withdrawing trifluoromethyl group contributed to increased stability and efficacy against resistant fungal strains. The research underscored the potential of 5-Amino-2-methoxy-3-(trifluoromethyl)pyridine in addressing global challenges in crop protection.

Recent synthetic methodologies have also focused on improving the accessibility of this compound. A 2023 paper in Organic Letters described a scalable, one-pot synthesis route for 5-Amino-2-methoxy-3-(trifluoromethyl)pyridine, reducing production costs and environmental impact. This advancement is expected to facilitate its broader adoption in industrial and academic settings.

In conclusion, 5-Amino-2-methoxy-3-(trifluoromethyl)pyridine (CAS: 1211584-76-7) continues to be a molecule of high interest due to its multifaceted applications in drug discovery and agrochemical development. Ongoing research is likely to uncover additional therapeutic and industrial uses, further solidifying its importance in the chemical biology and pharmaceutical industries.

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