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Atomfair 8-Quinolinamine, 3,4-dimethyl- C11H12N2

Description 3,4-Dimethylquinolin-8-amine (CAS No. 3510-66-5) is a high-purity heterocyclic organic compound with the molecular formula C11H12N2. This specialized quinoline derivative features a dimethyl-substituted quinoline core with an amine functional group at the 8-position, making it a valuable intermediate for pharmaceutical, agrochemical, and materials science research. Available as an off-white to light yellow crystalline powder with ??98% purity (HPLC), it is supplied in sealed packaging under inert atmosphere to ensure stability. Suitable for use in metal ligand synthesis, fluorescence studies, and as a building block for complex nitrogen-containing heterocycles. Store at 2-8??C in a dry environment protected from light.

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Description

Description

3,4-Dimethylquinolin-8-amine (CAS No. 3510-66-5) is a high-purity heterocyclic organic compound with the molecular formula C11H12N2. This specialized quinoline derivative features a dimethyl-substituted quinoline core with an amine functional group at the 8-position, making it a valuable intermediate for pharmaceutical, agrochemical, and materials science research. Available as an off-white to light yellow crystalline powder with ??98% purity (HPLC), it is supplied in sealed packaging under inert atmosphere to ensure stability. Suitable for use in metal ligand synthesis, fluorescence studies, and as a building block for complex nitrogen-containing heterocycles. Store at 2-8??C in a dry environment protected from light.

  • CAS No: 3510-66-5
  • Molecular Formula: C11H12N2
  • Molecular Weight: 172.23
  • Exact Mass: 172.100048391
  • Monoisotopic Mass: 172.100048391
  • IUPAC Name: 3,4-dimethylquinolin-8-amine
  • SMILES: CC1=CN=C2C(=C1C)C=CC=C2N
  • Synonyms: 3393-72-4, 8-Quinolinamine, 3,4-dimethyl-, 3,4-Dimethyl-8-aminoquinoline, Y8DT9MJ8LJ, EINECS 222-239-1

Application

3,4-Dimethylquinolin-8-amine serves as a key precursor in the synthesis of antimalarial and antimicrobial agents due to its structural similarity to clinically relevant quinoline scaffolds. Researchers utilize this compound to develop novel metal-organic frameworks (MOFs) and luminescent materials owing to its chelating amine functionality. In material science, it acts as a corrosion inhibitor and intermediate for dyes or organic semiconductors.

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