3-Amino-4-methoxy-1H-indazole

96%

Reagent Code: #137344
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CAS Number 886362-07-8

science Other reagents with same CAS 886362-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.18 g/mol
Formula C₈H₉N₃O
badge Registry Numbers
MDL Number MFCD08276946
thermostat Physical Properties
Melting Point 115-120 °C
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

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 due to its indazole core, which is known for promoting biological activity in drug candidates. Commonly employed in the preparation of selective inhibitors targeting enzymes involved in cell signaling pathways. Also utilized in research settings for the design of novel bioactive molecules with potential anti-inflammatory, antiviral, or neuroprotective properties. Its amino and methoxy functional groups allow for easy modification, enabling the creation of diverse compound libraries for high-throughput screening in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿2,260.00
3-Amino-4-methoxy-1H-indazole
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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 due to its indazole core, which is known for promoting biological activity in drug candidates. Commonly employed in the preparation of selective inhibitors targeting enzymes involved in cell signaling pathways. Also utilized in research settings for the design of novel bioactive molecules with potential ant

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 due to its indazole core, which is known for promoting biological activity in drug candidates. Commonly employed in the preparation of selective inhibitors targeting enzymes involved in cell signaling pathways. Also utilized in research settings for the design of novel bioactive molecules with potential anti-inflammatory, antiviral, or neuroprotective properties. Its amino and methoxy functional groups allow for easy modification, enabling the creation of diverse compound libraries for high-throughput screening in drug discovery.

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