5-Bromo-1H-indazole-7-carboxylic acid

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Reagent Code: #150398
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CAS Number 953409-99-9

science Other reagents with same CAS 953409-99-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.04 g/mol
Formula C₈H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD13177019
thermostat Physical Properties
Boiling Point 486.9±30.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, 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 form stable derivatives that interact with biological targets. Commonly employed in the preparation of potent and selective inhibitors targeting enzymes involved in cell signaling pathways. Its bromo and carboxylic acid functional groups allow for further chemical modifications through cross-coupling reactions and amide formation, making it valuable in drug discovery and optimization processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,370.00
inventory 250mg
10-20 days ฿3,220.00
inventory 1g
10-20 days ฿6,590.00
inventory 5g
10-20 days ฿32,950.00

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5-Bromo-1H-indazole-7-carboxylic acid
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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 derivatives that interact with biological targets. Commonly employed in the preparation of potent and selective inhibitors targeting enzymes involved in cell signaling pathways. Its bromo and carboxylic acid functional groups allow for further chemical modifications through

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 derivatives that interact with biological targets. Commonly employed in the preparation of potent and selective inhibitors targeting enzymes involved in cell signaling pathways. Its bromo and carboxylic acid functional groups allow for further chemical modifications through cross-coupling reactions and amide formation, making it valuable in drug discovery and optimization processes.

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