CAS 75696-17-2

6-Bromo-5-chloro-2-[(methylsulfinyl)acetyl]-3-(2-pyridyl)indole

Description:

6-Bromo-5-chloro-2-[(methylsulfinyl)acetyl]-3-(2-pyridyl)indole is a synthetic organic compound characterized by its complex structure, which includes an indole core substituted with various functional groups. The presence of bromine and chlorine atoms indicates that it is a halogenated compound, which can influence its reactivity and biological activity. The methylsulfinyl group suggests potential for interactions with biological systems, possibly enhancing its pharmacological properties. The acetyl group contributes to the compound's overall polarity and solubility, while the pyridyl moiety may enhance its ability to interact with biological targets, such as enzymes or receptors. This compound may exhibit interesting properties in medicinal chemistry, particularly in the development of pharmaceuticals, due to its diverse functional groups that can participate in various chemical reactions. Its specific applications and biological activities would depend on further studies, including in vitro and in vivo evaluations. As with many synthetic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

Formula: C₁₆H₁₂BrClN₂O₂S

InChI: InChI=1/C16H12BrClN2O2S/c1-23(22)8-14(21)16-15(12-4-2-3-5-19-12)9-6-11(18)10(17)7-13(9)20-16/h2-7,20H,8H2,1H3

Synonyms:

• 1-[6-Bromo-5-chloro-3-(2-pyridinyl)-1H-indol-2-yl]-2-(methylsulfinyl)ethanone
• 1-[6-bromo-5-chloro-3-(pyridin-2-yl)-1H-indol-2-yl]-2-(methylsulfinyl)ethanone
• Sch-24937
• Ethanone, 1-[6-bromo-5-chloro-3-(2-pyridinyl)-1H-indol-2-yl]-2-(methylsulfinyl)-

Sch 24937

CAS: 75696-17-2

Sch 24937 is a potent immunosuppressant on B lymphocyte mediated immune responses.

Formula: C₁₆H₁₂BrClN₂O₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 411.7

Ref: TM-T28708