7-Bromo-1H-pyrrolo[3,2-d]pyrimidin-4(5H)-one

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Reagent Code: #145748
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CAS Number 93587-23-6

science Other reagents with same CAS 93587-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.02 g/mol
Formula C₆H₄BrN₃O
badge Registry Numbers
MDL Number MFCD09999206
thermostat Physical Properties
Boiling Point 427.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for kinase inhibitors, which are important in the development of anticancer agents. Its structure allows for selective modifications, enabling the creation of derivatives with potential activity against various diseases, including inflammation and neurological disorders. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic purine bases in nucleotide-binding proteins.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿830.00
inventory 100mg
10-20 days ฿2,120.00

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7-Bromo-1H-pyrrolo[3,2-d]pyrimidin-4(5H)-one
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for kinase inhibitors, which are important in the development of anticancer agents. Its structure allows for selective modifications, enabling the creation of derivatives with potential activity against various diseases, including inflammation and neurological disorders. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studi

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for kinase inhibitors, which are important in the development of anticancer agents. Its structure allows for selective modifications, enabling the creation of derivatives with potential activity against various diseases, including inflammation and neurological disorders. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic purine bases in nucleotide-binding proteins.

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