(4-((4-(2-((tert-Butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)methyl)-2-fluorophenyl)boronic acid
98%
Reagent
Code: #89191
CAS Number
1704096-94-5
blur_circular Chemical Specifications
scatter_plot
Molecular Information
Weight
520.52 g/mol
Formula
C₂₉H₃₈BFN₂O₃Si
inventory_2
Storage & Handling
Storage
room temperature, dry
description Product Description
This compound is primarily utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is crucial in creating complex molecules, including drug candidates and biologically active compounds. The tert-butyldiphenylsilyl (TBDPS) protecting group in the structure helps stabilize the molecule during synthetic processes, allowing selective reactions to occur without interference. Its application is significant in the synthesis of targeted therapies, especially in cancer research, where boronic acid derivatives are explored for their potential as protease inhibitors. Additionally, the fluorophenyl moiety enhances the compound's ability to interact with biological targets, making it a promising intermediate in drug discovery.
shopping_cart Available Sizes & Pricing
Cart
No products
Subtotal:
0.00
Total
0.00
THB