1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

96%

Reagent Code: #209765
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CAS Number 885698-94-2

science Other reagents with same CAS 885698-94-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.1239 g/mol
Formula C₁₄H₁₉BN₂O₂
badge Registry Numbers
MDL Number MFCD10700158
thermostat Physical Properties
Melting Point 84-89°C
Boiling Point 384.979°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The indazole core contributes to biological activity in some targets, allowing for the construction of bioactive compounds and kinase inhibitors. Commonly employed in medicinal chemistry for late-stage functionalization due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿930.00
inventory 1g
10-20 days ฿2,580.00

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1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The indazole core contributes to biological activity in some targets, allowing for the construction of bioactive compounds and kinase inhibitors. Commonly employed in medicinal chemistry for late-stage functionalization due to its stability and reactivity profile.
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