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

97%

Reagent Code: #148225
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CAS Number 934560-92-6

science Other reagents with same CAS 934560-92-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.02 g/mol
Formula C₆H₄BrN₃
badge Registry Numbers
MDL Number MFCD13178164
thermostat Physical Properties
Boiling Point 399.1±42.0°C at 760 mmHg
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 for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of biologically active molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,310.00
inventory 250mg
10-20 days ฿5,170.00
inventory 1g
10-20 days ฿14,540.00
inventory 5g
10-20 days ฿47,560.00
inventory 10g
10-20 days ฿82,700.00

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6-Bromo-1H-pyrazolo[3,4-b]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of biologically active molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pestici

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo cross-coupling reactions, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of biologically active molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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