(5-Fluoro-1-methyl-1H-indazol-6-yl)boronic acid

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Reagent Code: #192576
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CAS Number 2096331-06-3

science Other reagents with same CAS 2096331-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.97 g/mol
Formula C₈H₈BFN₂O₂
badge Registry Numbers
MDL Number MFCD18089818
thermostat Physical Properties
Boiling Point 397.7±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.37±0.1 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. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of complex organic molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the indazole core’s ability to mimic purine bases, enhancing binding affinity to biological targets. Also utilized in the preparation of fluorescent probes and bioactive molecule labeling through boronate-based conjugation strategies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,080.00
inventory 250mg
10-20 days ฿6,990.00

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(5-Fluoro-1-methyl-1H-indazol-6-yl)boronic 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. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of complex organic molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the indazole core’s ability to mimic purine bases, enhancing binding affinity to biological targets. Also utilized in the preparation of fluorescent probes and bioactive molecule labeling through boronate-based conjugation strategies.
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