(6-Bromo-1H-indazol-3-yl)methanol

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Reagent Code: #55872
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CAS Number 885518-29-6

science Other reagents with same CAS 885518-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.0580 g/mol
Formula C₈H₇BrN₂O
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MDL Number MFCD07357298
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This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an indazole core and a bromo substituent, makes it a valuable building block for creating potential drug candidates. Researchers often employ it in the design of compounds targeting various biological pathways, including enzyme inhibition or receptor modulation. Its hydroxyl group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Additionally, it may be explored in the development of treatments for conditions such as cancer, inflammation, or neurological disorders, given the biological activity often associated with indazole derivatives.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿900.00
inventory 250mg
10-20 days ฿1,280.00
inventory 10g
10-20 days ฿28,450.00
inventory 1g
10-20 days ฿4,900.00

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(6-Bromo-1H-indazol-3-yl)methanol
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This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an indazole core and a bromo substituent, makes it a valuable building block for creating potential drug candidates. Researchers often employ it in the design of compounds targeting various biological pathways, including enzyme inhibition or receptor modulation. Its hydroxyl group allows for further functionalization, ena

This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an indazole core and a bromo substituent, makes it a valuable building block for creating potential drug candidates. Researchers often employ it in the design of compounds targeting various biological pathways, including enzyme inhibition or receptor modulation. Its hydroxyl group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Additionally, it may be explored in the development of treatments for conditions such as cancer, inflammation, or neurological disorders, given the biological activity often associated with indazole derivatives.

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