tert-Butyl 5-bromo-3-methyl-1H-pyrazolo[3,4-b]pyridine-1-carboxylate

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Reagent Code: #146421
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CAS Number 916258-24-7

science Other reagents with same CAS 916258-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.16 g/mol
Formula C₁₂H₁₄BrN₃O₂
badge Registry Numbers
MDL Number MFCD13183735
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in medicinal chemistry research for building pyrazolopyridine scaffolds, which exhibit a range of biological activities including anti-inflammatory and antiviral properties.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿530.00
inventory 100mg
10-20 days ฿1,590.00

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tert-Butyl 5-bromo-3-methyl-1H-pyrazolo[3,4-b]pyridine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in medicinal chemistry research for building pyrazolopyridine scaffolds, wh

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in medicinal chemistry research for building pyrazolopyridine scaffolds, which exhibit a range of biological activities including anti-inflammatory and antiviral properties.

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