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CAS 52430-43-0

:

2-Quinolinamine, N-methyl-

Description:
2-Quinolinamine, N-methyl- is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features an amino group (-NH2) at the 2-position and a methyl group (-CH3) attached to the nitrogen atom of the amino group, making it a derivative of quinoline. It is typically a solid at room temperature and may exhibit a range of physical properties, including solubility in organic solvents. The presence of the amino group allows for potential reactivity, including the ability to participate in hydrogen bonding and act as a nucleophile. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activity and utility in synthesizing other chemical entities. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C10H10N2
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Found 4 products.
  • N-Methylquinolin-2-amine

    CAS:
    Formula:C10H10N2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:158.1998

    Ref: IN-DA00DLCS

    1g
    131.00€
    100mg
    31.00€
    250mg
    51.00€
  • N-Methylquinolin-2-amine

    CAS:
    N-Methylquinolin-2-amine
    Purity:98%
    Molecular weight:158.204g/mol

    Ref: 54-OR74137

    1g
    174.00€
    5g
    684.00€
    100mg
    35.00€
    250mg
    53.00€
  • N-METHYLQUINOLIN-2-AMINE

    CAS:
    Formula:C10H10N2
    Purity:98%
    Molecular weight:158.204

    Ref: 10-F469057

    1g
    104.00€
    5g
    460.00€
    100mg
    21.00€
    250mg
    36.00€
  • N-Methylquinolin-2-amine

    CAS:
    <p>N-Methylquinolin-2-amine is a quinoline derivative that binds to the fatty acid ester of amides, which are found on the surface of cells. It has high specificity for hydroxy groups and is operational in aqueous solutions. N-Methylquinolin-2-amine has been shown to have activity against Alzheimer's disease by binding to the fatty acid ester of amide and blocking the function of ligands. The reaction time can be reduced by adding hydroxy group and alkyl group to the molecule. A molecular orbital diagram shows how this compound reacts with an amide substrate. This drug can be used as a diagnostic or postoperative treatment for Alzheimer's disease.</p>
    Formula:C10H10N2
    Purity:Min. 95%
    Molecular weight:158.2 g/mol

    Ref: 3D-CCA43043

    1g
    341.00€
    10g
    2,007.00€