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CAS 137354-54-2

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Quinoline, 4-(bromomethyl)-2-chloro-

Description:
Quinoline, 4-(bromomethyl)-2-chloro- is an organic compound that belongs to the class of quinolines, which are bicyclic aromatic compounds containing a fused benzene and pyridine ring. This specific compound features a bromomethyl group and a chlorine atom at the 4 and 2 positions, respectively, on the quinoline ring. It is typically characterized by its molecular structure, which contributes to its reactivity and potential applications in various chemical reactions, including nucleophilic substitutions and coupling reactions. The presence of halogen substituents, such as bromine and chlorine, often enhances the compound's reactivity, making it useful in synthetic organic chemistry. Quinoline derivatives are known for their biological activity, and this compound may exhibit properties relevant to pharmaceuticals or agrochemicals. Additionally, it may be soluble in organic solvents and exhibit moderate stability under standard conditions. Safety data should be consulted for handling, as halogenated compounds can pose health and environmental risks.
Formula:C10H7BrClN
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Found 3 products.
  • 4-(bromomethyl)-2-chloroquinoline

    CAS:
    Formula:C10H7BrClN
    Molecular weight:256.5263

    Ref: IN-DA001360

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  • 4-BROMOMETHYL-2-CHLOROQUINOLINE

    CAS:
    Formula:C10H7BrClN
    Purity:97.0%
    Molecular weight:256.53

    Ref: 10-F300927

    1g
    620.00€
    250mg
    264.00€
  • 4-bromomethyl-2-chloroquinoline

    CAS:
    <p>4-Bromomethyl-2-chloroquinoline is an organic compound that contains a pyrrole ring and an alkyl group. It is synthesized by the reaction of 4-bromomethylbenzene with quinoline. This product has been shown to be efficacious against tumor cells in vitro and in vivo, and has antitumor activity. 4-Bromomethyl-2-chloroquinoline is also used as a building block for the synthesis of other heterocyclic compounds. The efficiency of this process depends on the metalation of the pyrrole ring. Lithiation, for example, leads to increased reactivity due to increased electron density on the ring. Alkylation occurs when a reactive alkylating agent reacts with one or more of the bromine atoms on the pyrrole ring, leading to cleavage of carbon bonds in the ring and formation of new bonds between carbon atoms. This reaction</p>
    Formula:C10H7BrClN
    Purity:Min. 95%
    Molecular weight:256.53 g/mol

    Ref: 3D-MFA35454

    250mg
    420.00€
    2500mg
    1,247.00€