tert-Butyl 1-(1H-indol-3-yl)isoquinoline-2(1H)-carboxylate

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Reagent Code: #39117
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CAS Number 1612888-20-6

science Other reagents with same CAS 1612888-20-6

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Weight 346.4223 g/mol
Formula C₂₂H₂₂N₂O₂
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both indole and isoquinoline moieties, makes it a valuable building block for developing potential drug candidates, particularly in the areas of oncology and neurology. Researchers leverage its framework to design and optimize compounds that target specific enzymes or receptors involved in disease pathways. Additionally, it is employed in the study of structure-activity relationships (SAR) to enhance the efficacy and selectivity of therapeutic agents. Its application extends to chemical biology, where it aids in the exploration of cellular mechanisms and the development of novel inhibitors or modulators for various biological processes.

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

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tert-Butyl 1-(1H-indol-3-yl)isoquinoline-2(1H)-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both indole and isoquinoline moieties, makes it a valuable building block for developing potential drug candidates, particularly in the areas of oncology and neurology. Researchers leverage its framework to design and optimize compounds that target specific enzymes or receptors involved in disease pathways. Additionally, it is employed in t
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both indole and isoquinoline moieties, makes it a valuable building block for developing potential drug candidates, particularly in the areas of oncology and neurology. Researchers leverage its framework to design and optimize compounds that target specific enzymes or receptors involved in disease pathways. Additionally, it is employed in the study of structure-activity relationships (SAR) to enhance the efficacy and selectivity of therapeutic agents. Its application extends to chemical biology, where it aids in the exploration of cellular mechanisms and the development of novel inhibitors or modulators for various biological processes.
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