3-(tert-butyl)-8-chloro-1-iodoimidazo[1,5-a]pyrazine

97%

Reagent Code: #239559
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CAS Number 1211524-21-8

science Other reagents with same CAS 1211524-21-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 335.57 g/mol
Formula C₁₀H₁₁ClIN₃
badge Registry Numbers
MDL Number MFCD20489129
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in creating potent bioactive molecules. It is also employed in research settings to develop novel neuroprotective agents and antiviral drugs due to its ability to cross biological membranes and interact with specific enzyme targets. Commonly utilized in late-stage functionalization reactions in medicinal chemistry for rapid compound optimization.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,670.00
3-(tert-butyl)-8-chloro-1-iodoimidazo[1,5-a]pyrazine
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in creating potent bioactive molecules. It is also employed in research settings to develop novel neuroprotective agents and antiviral drugs due to its ability to cross biological membranes and interact with specific enzyme targets. Commonly utilized in late-stage functiona

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in creating potent bioactive molecules. It is also employed in research settings to develop novel neuroprotective agents and antiviral drugs due to its ability to cross biological membranes and interact with specific enzyme targets. Commonly utilized in late-stage functionalization reactions in medicinal chemistry for rapid compound optimization.

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