6-Bromo-1H-indazole-3-carboxylic acid

97%

Reagent Code: #148180
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CAS Number 660823-36-9

science Other reagents with same CAS 660823-36-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.04 g/mol
Formula C₈H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD05663977
thermostat Physical Properties
Boiling Point 493.361°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

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 substituted indazole derivatives, which are present in various biologically active molecules. Commonly employed in research settings to design drugs targeting inflammatory diseases, neurological disorders, and tumor growth. Its carboxylic acid and bromo functional groups allow for further chemical modifications through coupling reactions or nucleophilic substitutions, making it valuable in creating compound libraries for drug discovery.

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Test Parameter Specification
Appearance White to off-white solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿170.50
inventory 250mg
10-20 days ฿198.00
inventory 1g
10-20 days ฿709.50

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6-Bromo-1H-indazole-3-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 substituted indazole derivatives, which are present in various biologically active molecules. Commonly employed in research settings to design drugs targeting inflammatory diseases, neurological disorders, and tumor growth. Its carboxylic acid and bromo functional groups allow for

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 substituted indazole derivatives, which are present in various biologically active molecules. Commonly employed in research settings to design drugs targeting inflammatory diseases, neurological disorders, and tumor growth. Its carboxylic acid and bromo functional groups allow for further chemical modifications through coupling reactions or nucleophilic substitutions, making it valuable in creating compound libraries for drug discovery.

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