6-Bromo-3-methoxy-1-phenyl-1H-indazole

95%

Reagent Code: #148120
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CAS Number 1332527-03-3

science Other reagents with same CAS 1332527-03-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.15 g/mol
Formula C₁₄H₁₁BrN₂O
badge Registry Numbers
MDL Number MFCD27939304
thermostat Physical Properties
Boiling Point 356.6±24.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.47±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing kinase inhibitors and other agents targeting inflammatory and oncological pathways. Its bromo and methoxy functional groups allow for selective modifications via cross-coupling reactions, making it valuable in structure-activity relationship studies. Also explored in the development of cannabinoid receptor modulators due to the indazole core’s affinity for such targets. Not intended for use in food, consumer products, or human therapeutics without extensive safety evaluation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,610.00
inventory 250mg
10-20 days ฿6,500.00
inventory 1g
10-20 days ฿17,030.00

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6-Bromo-3-methoxy-1-phenyl-1H-indazole
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Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing kinase inhibitors and other agents targeting inflammatory and oncological pathways. Its bromo and methoxy functional groups allow for selective modifications via cross-coupling reactions, making it valuable in structure-activity relationship studies. Also explored in the development of cannabinoid receptor modulators due to the indazole core’s affinity for suc

Used primarily in pharmaceutical research as an intermediate in the synthesis of bioactive compounds. It serves as a building block for developing kinase inhibitors and other agents targeting inflammatory and oncological pathways. Its bromo and methoxy functional groups allow for selective modifications via cross-coupling reactions, making it valuable in structure-activity relationship studies. Also explored in the development of cannabinoid receptor modulators due to the indazole core’s affinity for such targets. Not intended for use in food, consumer products, or human therapeutics without extensive safety evaluation.

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