4-Bromo-6-chloro-1H-indazole

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Reagent Code: #146252
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CAS Number 885519-03-9

science Other reagents with same CAS 885519-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.48 g/mol
Formula C₇H₄BrClN₂
badge Registry Numbers
MDL Number MFCD07781352
thermostat Physical Properties
Melting Point 219-221°C
inventory_2 Storage & Handling
Storage Room temperature, 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 cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing bioactive molecules with potential anti-inflammatory, antiviral, and antitumor activities. Its halogenated structure allows for further functionalization via palladium-catalyzed reactions, making it valuable in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,570.00
inventory 10g
10-20 days ฿6,440.00
inventory 25g
10-20 days ฿12,800.00
inventory 100g
10-20 days ฿48,000.00

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4-Bromo-6-chloro-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 undergo selective cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing bioactive molecules with potential anti-inflammatory, antiviral, and antitumor activities. Its halogenated structure allows for fu

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 cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing bioactive molecules with potential anti-inflammatory, antiviral, and antitumor activities. Its halogenated structure allows for further functionalization via palladium-catalyzed reactions, making it valuable in drug discovery and development.

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