3-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxamide

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Reagent Code: #44638
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CAS Number 395101-84-5

science Other reagents with same CAS 395101-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.17 g/mol
Formula C₁₃H₁₄BrN₃O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of compounds targeting specific enzymes or receptors, often in the context of drug discovery for diseases such as cancer or inflammatory disorders. Its structure, featuring a bromoindazole moiety, makes it valuable for further functionalization through cross-coupling reactions, enabling the development of diverse therapeutic agents. Additionally, the tetrahydro-2H-pyran protecting group enhances its stability during synthetic processes, facilitating its use in complex multi-step reactions.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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3-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxamide
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of compounds targeting specific enzymes or receptors, often in the context of drug discovery for diseases such as cancer or inflammatory disorders. Its structure, featuring a bromoindazole moiety, makes it valuable for further functionalization through cross-coupling reactions, enabling the development of diverse thera
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of compounds targeting specific enzymes or receptors, often in the context of drug discovery for diseases such as cancer or inflammatory disorders. Its structure, featuring a bromoindazole moiety, makes it valuable for further functionalization through cross-coupling reactions, enabling the development of diverse therapeutic agents. Additionally, the tetrahydro-2H-pyran protecting group enhances its stability during synthetic processes, facilitating its use in complex multi-step reactions.
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