3-Bromo-4-chloro-1H-pyrazolo[3,4-b]pyridine

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Reagent Code: #65117
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CAS Number 1357945-38-0

science Other reagents with same CAS 1357945-38-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.47 g/mol
Formula C₆H₃BrClN₃
badge Registry Numbers
MDL Number MFCD22380452
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents, especially those targeting kinase inhibition. Researchers often employ it to create novel compounds with potential therapeutic applications, such as anti-cancer, anti-inflammatory, or anti-viral drugs. Additionally, its unique pyrazolo[3,4-b]pyridine core makes it a versatile building block in organic synthesis, enabling the exploration of new chemical spaces for drug discovery. Its halogenated nature also allows for further functionalization, enhancing its utility in designing complex molecules with specific biological activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,064.00
inventory 250mg
10-20 days ฿13,698.00
inventory 1g
10-20 days ฿36,972.00

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3-Bromo-4-chloro-1H-pyrazolo[3,4-b]pyridine
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents, especially those targeting kinase inhibition. Researchers often employ it to create novel compounds with potential therapeutic applications, such as anti-cancer, anti-inflammatory, or anti-viral drugs. Additionally, its unique pyrazolo[3,4-b]pyridine core makes it a versatile building block in organic synthesis, enabling the exploration of new chemical spaces for drug discovery. Its halogenated nature also allows for further functionalization, enhancing its utility in designing complex molecules with specific biological activities.
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