6-(Benzyloxy)-4-fluoro-1H-indazole

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Reagent Code: #150349
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CAS Number 1253792-35-6

science Other reagents with same CAS 1253792-35-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.25 g/mol
Formula C₁₄H₁₁FN₂O
badge Registry Numbers
MDL Number MFCD19443332
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to anti-inflammatory and anticancer agents due to its indazole core, which is known for interacting with various enzyme targets. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates targeting neurological disorders and metabolic diseases. Its fluorinated and benzyloxy-modified structure enhances binding selectivity and metabolic stability in experimental therapeutics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,000.00
inventory 250mg
10-20 days ฿11,120.00
inventory 1g
10-20 days ฿28,840.00

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6-(Benzyloxy)-4-fluoro-1H-indazole
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Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to anti-inflammatory and anticancer agents due to its indazole core, which is known for interacting with various enzyme targets. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates targeting neurological disorders and metabolic diseases. Its fluorinate

Used in pharmaceutical research as an intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to anti-inflammatory and anticancer agents due to its indazole core, which is known for interacting with various enzyme targets. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates targeting neurological disorders and metabolic diseases. Its fluorinated and benzyloxy-modified structure enhances binding selectivity and metabolic stability in experimental therapeutics.

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