tert-Butyl 4-chloro-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate

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Reagent Code: #148651
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CAS Number 1053657-15-0

science Other reagents with same CAS 1053657-15-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.70 g/mol
Formula C₁₁H₁₄ClN₃O₂
badge Registry Numbers
MDL Number MFCD08273924
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure allows for selective modification, making it valuable in creating active ingredients for targeted cancer therapies. Commonly employed in medicinal chemistry for constructing pyrrolopyrimidine-based scaffolds, which exhibit biological activity against various disease targets. Also utilized in research settings to develop novel drug candidates due to its reactivity and functional group compatibility in cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,660.00
inventory 250mg
10-20 days ฿3,400.00
inventory 1g
10-20 days ฿9,340.00
inventory 5g
10-20 days ฿40,480.00

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tert-Butyl 4-chloro-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure allows for selective modification, making it valuable in creating active ingredients for targeted cancer therapies. Commonly employed in medicinal chemistry for constructing pyrrolopyrimidine-based scaffolds, which exhibit biological activity against various disease targets. Also utilized in research settings to develop novel drug candidates due to its reactivity an

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure allows for selective modification, making it valuable in creating active ingredients for targeted cancer therapies. Commonly employed in medicinal chemistry for constructing pyrrolopyrimidine-based scaffolds, which exhibit biological activity against various disease targets. Also utilized in research settings to develop novel drug candidates due to its reactivity and functional group compatibility in cross-coupling reactions.

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