4-Bromo-1H-indazol-6-ol

97%

Reagent Code: #141083
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CAS Number 885518-75-2

science Other reagents with same CAS 885518-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.03 g/mol
Formula C₇H₅BrN₂O
badge Registry Numbers
MDL Number MFCD07781338
thermostat Physical Properties
Boiling Point 412.7±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.941±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, 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 ability to undergo selective functionalization at the bromo position, enabling the formation of C-C and C-N bonds. Commonly employed in the preparation of biologically active molecules targeting inflammation, neurodegenerative diseases, and metabolic disorders. Its indazole core provides structural stability and favorable interactions with enzyme active sites, making it valuable in drug discovery research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,260.00
inventory 500mg
10-20 days ฿21,890.00
4-Bromo-1H-indazol-6-ol
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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 undergo selective functionalization at the bromo position, enabling the formation of C-C and C-N bonds. Commonly employed in the preparation of biologically active molecules targeting inflammation, neurodegenerative diseases, and metabolic disorders. Its indazole core provides structur

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 undergo selective functionalization at the bromo position, enabling the formation of C-C and C-N bonds. Commonly employed in the preparation of biologically active molecules targeting inflammation, neurodegenerative diseases, and metabolic disorders. Its indazole core provides structural stability and favorable interactions with enzyme active sites, making it valuable in drug discovery research.

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