6-Bromo-2-butyl-1H-benz[de]isoquinoline-1,3(2H)-dione

≥98.0%(GC)(T)

Reagent Code: #141592
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CAS Number 92874-17-4

science Other reagents with same CAS 92874-17-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.2 g/mol
Formula C₁₆H₁₄BrNO₂
badge Registry Numbers
MDL Number MFCD28033162
thermostat Physical Properties
Melting Point 104 °C
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. Its structure allows for selective modification to target specific enzymes involved in tumor growth. Commonly employed in medicinal chemistry research for optimizing drug candidates due to its ability to enhance binding affinity and metabolic stability. Also utilized in the preparation of fluorescent probes for studying cellular processes, leveraging its aromatic framework for signal detection.

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inventory 1g
10-20 days ฿4,300.00

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6-Bromo-2-butyl-1H-benz[de]isoquinoline-1,3(2H)-dione
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Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. Its structure allows for selective modification to target specific enzymes involved in tumor growth. Commonly employed in medicinal chemistry research for optimizing drug candidates due to its ability to enhance binding affinity and metabolic stability. Also utilized in the preparation of fluorescent probes for studying cellular processes, leveraging its aromatic framework for signal de

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. Its structure allows for selective modification to target specific enzymes involved in tumor growth. Commonly employed in medicinal chemistry research for optimizing drug candidates due to its ability to enhance binding affinity and metabolic stability. Also utilized in the preparation of fluorescent probes for studying cellular processes, leveraging its aromatic framework for signal detection.

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