6-Bromo-1H-indazole

98%

Reagent Code: #143777
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CAS Number 79762-54-2

science Other reagents with same CAS 79762-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.03 g/mol
Formula C₇H₅BrN₂
badge Registry Numbers
MDL Number MFCD03265457
thermostat Physical Properties
Melting Point 180-182 °C
inventory_2 Storage & Handling
Storage Room temperature

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 ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in research settings to design drugs targeting inflammatory diseases, neurodegenerative disorders, and various solid tumors. Its bromine functionality allows for further chemical modifications through cross-coupling reactions, enabling rapid diversification in drug discovery programs. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿154.00
inventory 25g
10-20 days ฿1,640.00
inventory 100g
10-20 days ฿6,280.00
inventory 500g
10-20 days ฿29,370.00
inventory 5g
10-20 days ฿520.00

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6-Bromo-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 ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in research settings to design drugs targeting inflammatory diseases, neurodegenerative disorders, and various solid tumors. Its bromine functionality allows for further chemical modifications

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 ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in research settings to design drugs targeting inflammatory diseases, neurodegenerative disorders, and various solid tumors. Its bromine functionality allows for further chemical modifications through cross-coupling reactions, enabling rapid diversification in drug discovery programs. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies.

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