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CAS 52263-84-0

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(S)-α-Methyl-6-chloro-9H-carbazole-2-acetic acid

Description:
(S)-α-Methyl-6-chloro-9H-carbazole-2-acetic acid is a chemical compound characterized by its unique structure, which includes a carbazole moiety, a chlorine atom, and an acetic acid functional group. This compound is typically classified as a chiral molecule due to the presence of a stereocenter, which contributes to its specific optical activity. The chlorine substituent at the 6-position of the carbazole ring enhances its biological activity and may influence its pharmacological properties. The acetic acid group provides acidic characteristics, allowing for potential interactions in biological systems. This compound may exhibit various biological activities, including anti-inflammatory or analgesic effects, making it of interest in medicinal chemistry. Its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups. Overall, (S)-α-Methyl-6-chloro-9H-carbazole-2-acetic acid represents a significant compound in the study of pharmaceuticals and organic synthesis.
Formula:C15H12ClNO2
Synonyms:
  • 9H-Carbazole-2-acetic acid, 6-chloro-α-methyl-, (αS)-
  • (S)-6-Chloro-α-methyl-9H-carbazole-2-acetic acid
  • C 8012
  • (S)-α-Methyl-6-chloro-9H-carbazole-2-acetic acid
  • (S)-Carprofen
  • (S)-2-(6-Chloro-9H-carbazol-2-yl)propanoic acid
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Found 3 products.
  • (S)-Carprofen
    Biosynth
    + Info

    (S)-Carprofen

    CAS:
    <p>Carprofen is a nonsteroidal anti-inflammatory drug (NSAID) that is used to treat pain and inflammation in dogs. It is also used for the management of postoperative pain, as well as for the treatment of osteoarthritis, rheumatoid arthritis, and other conditions. Carprofen has been shown to inhibit cyclooxygenase-2 (COX-2) activity and prostaglandin synthesis. The inhibition potential of carprofen has been determined by the modification of COX-2 by S-carprofen and its stereoselectivity. This study also showed that carprofen inhibits lipase activity in an ex vivo model of canine blood plasma, which may be related to its effects on endogenous substances such as leukotrienes. Carprofen has been shown to reduce inflammation and pain in animal models through the inhibition of COX-2 activity and prostaglandin synthesis. The time required for this reaction is less than</p>
    Formula:C15H12ClNO2
    Purity:Min. 95%
    Color and Shape:White To Off-White Solid
    Molecular weight:273.71 g/mol

    Ref: 3D-FC19825

    5mg
    363.00€
    10mg
    489.00€
  • (S)-Carprofen-D3
    TRC
    + Info

    (S)-Carprofen-D3

    Controlled Product
    CAS:
    Formula:C15D3H9ClNO2
    Color and Shape:Neat
    Molecular weight:276.733

    Ref: TR-C184347

    25mg
    10,516.00€
  • (S)-Carprofen
    TRC
    + Info

    (S)-Carprofen

    Controlled Product
    CAS:
    Formula:C15H12ClNO2
    Color and Shape:Neat
    Molecular weight:273.71

    Ref: TR-C184345

    2500µg
    303.00€