tert-Butyl 6-fluoro-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate

≥95%

Reagent Code: #120468
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CAS Number 1333222-21-1

science Other reagents with same CAS 1333222-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.23 g/mol
Formula C₁₉H₂₆BFN₂O₄
badge Registry Numbers
MDL Number MFCD17677331
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a boronate ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is crucial in the development of pharmaceuticals, particularly in creating complex molecules for drug discovery and development. The presence of the indazole core further enhances its utility in designing compounds with potential therapeutic applications, such as kinase inhibitors or anti-cancer agents. Additionally, the tert-butyl carboxylate group provides stability and facilitates further chemical modifications, making it a versatile building block in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,490.00

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tert-Butyl 6-fluoro-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a boronate ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is crucial in the development of pharmaceuticals, particularly in creating complex molecules for drug discovery and development. The presence of the indazole core further enhances its utility in designing compounds with potential therapeutic applications, such as kinase inhibitors or anti-cancer agents. Additionally, the tert-butyl carboxylate group provides stability and facilitates further chemical modifications, making it a versatile building block in organic synthesis.
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