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CAS 66473-14-1

:

Benzenesulfonamide, N-butyl-4-nitro-

Description:
Benzenesulfonamide, N-butyl-4-nitro- is an organic compound characterized by the presence of a sulfonamide group attached to a benzene ring, along with a butyl group and a nitro group at the para position of the aromatic ring. This compound typically exhibits properties associated with both sulfonamides and nitro compounds, such as moderate solubility in organic solvents and potential reactivity due to the presence of the nitro group. The sulfonamide moiety contributes to its potential as a pharmaceutical intermediate, while the nitro group can influence its electronic properties and reactivity. The compound may also display biological activity, which is common among sulfonamide derivatives, making it of interest in medicinal chemistry. Additionally, its structure suggests that it could participate in various chemical reactions, including nucleophilic substitutions and reductions, depending on the reaction conditions. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity and environmental impact.
Formula:C10H14N2O4S
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Found 3 products.
  • N-Butyl-4-nitrobenzenesulfonamide

    CAS:
    Formula:C10H14N2O4S
    Molecular weight:258.2942

    Ref: IN-DA00FGYP

    ne
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  • N-Butyl-4-nitrobenzenesulfonamide

    CAS:
    Formula:C10H14N2O4S
    Purity:95.0%
    Molecular weight:258.29

    Ref: 10-F212243

    1g
    235.00€
  • N-Butyl-4-nitrobenzenesulfonamide

    CAS:
    <p>N-Butyl-4-nitrobenzenesulfonamide is a chemical compound that belongs to the group of nitro compounds. It is synthesized by the reaction of an aliphatic amine with nitrobenzenesulfonyl chloride. The structure of this compound is characterized by an electron-deficient phenyl ring, which can be protonated and form a radical anion. N-Butyl-4-nitrobenzenesulfonamide has been shown to yield nitrated aliphatic amines, such as 3-nitropropane sulfonamide, when treated with sodium nitrate in dilute sulfuric acid. This chemical reaction occurs through radical ion mechanisms and involves the cleavage of a bond between two carbon atoms.</p>
    Formula:C10H14N2O4S
    Purity:Min. 95%
    Molecular weight:258.3 g/mol

    Ref: 3D-RCA47314

    2500mg
    444.00€