6-Bromo-1H-indazole-3-carbaldehyde

98%

Reagent Code: #145711
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CAS Number 885271-72-7

science Other reagents with same CAS 885271-72-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.04 g/mol
Formula C₈H₅BrN₂O
thermostat Physical Properties
Boiling Point 414.1°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

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 for constructing biologically active molecules due to its ability to undergo selective functionalization at the bromo and aldehyde sites. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to expand molecular complexity. Also utilized in the preparation of indazole-based derivatives with potential anti-inflammatory, antiviral, and neuroprotective activities. Its structural features make it valuable in drug discovery programs targeting central nervous system disorders and oncology.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,170.00
inventory 5g
10-20 days ฿4,310.00
inventory 10g
10-20 days ฿8,600.00
inventory 25g
10-20 days ฿13,650.00
6-Bromo-1H-indazole-3-carbaldehyde
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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 for constructing biologically active molecules due to its ability to undergo selective functionalization at the bromo and aldehyde sites. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to expand molecular complexity. Also utilized in the preparation of indazole-based derivati

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 for constructing biologically active molecules due to its ability to undergo selective functionalization at the bromo and aldehyde sites. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to expand molecular complexity. Also utilized in the preparation of indazole-based derivatives with potential anti-inflammatory, antiviral, and neuroprotective activities. Its structural features make it valuable in drug discovery programs targeting central nervous system disorders and oncology.

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