7-Bromo-5-methylindoline-2,3-dione

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Reagent Code: #156006
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CAS Number 108938-16-5

science Other reagents with same CAS 108938-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.05 g/mol
Formula C₉H₆BrNO₂
badge Registry Numbers
MDL Number MFCD00462954
thermostat Physical Properties
Melting Point 176-180 °C
inventory_2 Storage & Handling
Density 1.714±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for designing bioactive molecules. Also employed in the preparation of indirubin derivatives, which show potential in treating neurodegenerative diseases and inflammation. Commonly utilized in research settings for structure-activity relationship (SAR) studies due to its reactive sites and stability in various coupling reactions.

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inventory 1g
10-20 days ฿7,140.00

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7-Bromo-5-methylindoline-2,3-dione
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for designing bioactive molecules. Also employed in the preparation of indirubin derivatives, which show potential in treating neurodegenerative diseases and inflammation. Commonly utilized in research settings for structure-activity relationship (SAR) studies due

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for designing bioactive molecules. Also employed in the preparation of indirubin derivatives, which show potential in treating neurodegenerative diseases and inflammation. Commonly utilized in research settings for structure-activity relationship (SAR) studies due to its reactive sites and stability in various coupling reactions.

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