7-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

98%

Reagent Code: #155669
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CAS Number 1158680-89-7

science Other reagents with same CAS 1158680-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.15 g/mol
Formula C₁₂H₁₃BrN₂O
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for indazole-based derivatives that show potential in medicinal chemistry, including kinase inhibitors and CNS-targeted agents. The bromo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification for structure-activity relationship studies. The tetrahydropyranyl (THP) protecting group enhances solubility and stability during synthetic transformations, and can be removed under mild acidic conditions when needed. Commonly employed in the development of drug candidates targeting inflammation, cancer, and neurological disorders.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,020.00
250mg
10-20 days ฿7,690.00
1g
10-20 days ฿28,810.00
7-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for indazole-based derivatives that show potential in medicinal chemistry, including kinase inhibitors and CNS-targeted agents. The bromo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification for structure-activity relationship studies. The tetrahydropyranyl (THP) protecting grou

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for indazole-based derivatives that show potential in medicinal chemistry, including kinase inhibitors and CNS-targeted agents. The bromo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification for structure-activity relationship studies. The tetrahydropyranyl (THP) protecting group enhances solubility and stability during synthetic transformations, and can be removed under mild acidic conditions when needed. Commonly employed in the development of drug candidates targeting inflammation, cancer, and neurological disorders.

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