4-Oxo-4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amino)butanoic acid

96%

Reagent Code: #222363
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CAS Number 480424-98-4

science Other reagents with same CAS 480424-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.16 g/mol
Formula C₁₆H₂₂BNO₅
badge Registry Numbers
MDL Number MFCD03789267
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, especially in the development of kinase inhibitors for cancer treatment. Its boronic ester functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl systems found in bioactive molecules. It is also employed in medicinal chemistry for modifying peptide-like structures to enhance binding affinity and metabolic stability. Additionally, it serves as a building block in the preparation of proteolysis-targeting chimeras (PROTACs) due to its ability to link target-binding ligands with E3 ligase recruiters.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,500.00
inventory 1g
10-20 days ฿3,470.00
inventory 5g
10-20 days ฿11,220.00
inventory 25g
10-20 days ฿36,230.00
4-Oxo-4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amino)butanoic acid
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, especially in the development of kinase inhibitors for cancer treatment. Its boronic ester functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl systems found in bioactive molecules. It is also employed in medicinal chemistry for modifying peptide-like structures to enhance binding affinity and metabolic stability. Additionally, it serves as a building block

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, especially in the development of kinase inhibitors for cancer treatment. Its boronic ester functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl systems found in bioactive molecules. It is also employed in medicinal chemistry for modifying peptide-like structures to enhance binding affinity and metabolic stability. Additionally, it serves as a building block in the preparation of proteolysis-targeting chimeras (PROTACs) due to its ability to link target-binding ligands with E3 ligase recruiters.

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