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CAS 157494-40-1

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4-Chloro-3-QuinolinesulfonylChloride

Description:
4-Chloro-3-quinolinesulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group attached to a quinoline ring system. This compound typically appears as a solid and is known for its reactivity, particularly due to the presence of the sulfonyl chloride group, which can participate in nucleophilic substitution reactions. It is often utilized in organic synthesis, particularly in the preparation of sulfonamide derivatives and other complex organic molecules. The chlorine atom at the 4-position of the quinoline ring enhances its electrophilic character, making it a valuable intermediate in various chemical reactions. Additionally, this compound may exhibit biological activity, which can be explored in medicinal chemistry. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with sulfonyl chlorides. As with many chemical substances, it is important to consult safety data sheets and relevant literature for specific handling guidelines and potential hazards.
Formula:C9H5Cl2NO2S
Synonyms:
  • 4-chloroquinoline-3-sulfonyl chloride
  • 3-Quinolinesulfonyl chloride, 4-chloro-
  • 4-Chloro-3-QuinolinesulfonylChloride
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Found 2 products.
  • 4-Chloroquinoline-3-sulfonyl chloride
    Indagoo
    + Info

    4-Chloroquinoline-3-sulfonyl chloride

    CAS:
    Formula:C9H5Cl2NO2S
    Color and Shape:Solid
    Molecular weight:262.1125

    Ref: IN-DA001PGV

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  • 4-Chloroquinoline-3-sulfonyl chloride
    Biosynth
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    4-Chloroquinoline-3-sulfonyl chloride

    CAS:
    <p>4-Chloroquinoline-3-sulfonyl chloride is an analog of chloride and chlorine. It is a halide that is used in organic synthesis as a one-step conversion of benzene to the sulfone. 4-Chloroquinoline-3-sulfonyl chloride can be synthesized by reacting chloroacetic acid with sulfur trioxide. This chemical has been shown to be effective in x-ray crystallography and nmr data. It has also been used to study the mechanism of ether cleavage, hydrolysis, and tautomerism. The sodium salt of 4-chloroquinoline-3-sulfonyl chloride has been shown to release hydrogen sulfide when dissolved in water or alcohol with at least one hydroxyl group.</p>
    Formula:C9H5Cl2NO2S
    Purity:Min. 95%
    Molecular weight:262.11 g/mol

    Ref: 3D-HGA49440

    50mg
    503.00€
    500mg
    1,383.00€