CAS 76086-99-2
:2H-Indol-2-one, 3-[(4-bromophenyl)methylene]-1,3-dihydro-
Description:
2H-Indol-2-one, 3-[(4-bromophenyl)methylene]-1,3-dihydro- is a chemical compound characterized by its indole structure, which features a fused bicyclic system consisting of a benzene ring and a pyrrole ring. The presence of a methylene bridge connecting the 3-position of the indole to a 4-bromophenyl group introduces significant steric and electronic effects, influencing its reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its bromine substituent can enhance lipophilicity and may also play a role in biological interactions, making it of interest in medicinal chemistry. The compound may exhibit various properties such as fluorescence or photostability, depending on its specific molecular interactions. Additionally, it may be studied for its potential applications in pharmaceuticals, particularly in the development of new therapeutic agents. As with many indole derivatives, it may also show interesting properties in terms of antioxidant or anti-inflammatory activities.
Formula:C15H10BrNO
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
2H-Indol-2-one, 3-[(4-bromophenyl)methylene]-1,3-dihydro-
CAS:Formula:C15H10BrNOPurity:99%Color and Shape:SolidMolecular weight:300.1500SU 4942
CAS:<p>SU-4942 is a modulator of tyrosine kinase signaling.</p>Formula:C15H10BrNOPurity:99% - 99.32%Color and Shape:SolidMolecular weight:300.15SU 4942
CAS:<p>SU 4942 is an analog of the anilinoquinazoline class of compounds, which are tyrosine kinase inhibitors. SU 4942 binds to and inhibits the activity of protein tyrosine kinases in cells, preventing the transformation of growth factors into active forms that regulate cell proliferation and survival. SU 4942 has been shown to prevent atherosclerosis in animal models by decreasing the deposition of lipids in blood vessels. This drug also prevents cancer by inducing apoptosis and suppressing angiogenesis.</p>Formula:C15H10BrNOPurity:Min. 95%Molecular weight:300.16 g/mol




