4-Bromo-6-methoxy-1H-indazole

≥97%

Reagent Code: #148280
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CAS Number 885520-83-2

science Other reagents with same CAS 885520-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.06 g/mol
Formula C₈H₇BrN₂O
badge Registry Numbers
MDL Number MFCD08272208
thermostat Physical Properties
Boiling Point 360.9±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

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 cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing potent and selective bioactive molecules, especially in oncology and inflammation-related drug discovery programs. Its bromo and methoxy functional groups allow for selective modifications, making it valuable in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,660.00
inventory 1g
10-20 days ฿11,410.00

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4-Bromo-6-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 ability to undergo cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing potent and selective bioactive molecules, especially in oncology and inflammation-related drug discovery programs. Its bromo and methoxy fun

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 cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing potent and selective bioactive molecules, especially in oncology and inflammation-related drug discovery programs. Its bromo and methoxy functional groups allow for selective modifications, making it valuable in structure-activity relationship (SAR) studies.

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