(4-((2-Acrylamidoethyl)carbamoyl)-3-fluorophenyl)boronic acid

95%

Reagent Code: #89178
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CAS Number 1313712-90-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.06 g/mol
Formula C₁₂H₁₄BFN₂O₄
badge Registry Numbers
MDL Number MFCD32856191
inventory_2 Storage & Handling
Storage 2-8 ℃, inert gas storage

description Product Description

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its boronic acid functional group, which is known for its ability to form stable covalent bonds with diols and other nucleophiles. It is often employed in the development of boron-containing drugs, particularly in the synthesis of protease inhibitors and other therapeutic agents targeting specific enzymes. Additionally, its acrylamide moiety makes it suitable for polymerization reactions, enabling its use in the creation of advanced materials such as hydrogels or molecularly imprinted polymers. These materials have applications in drug delivery systems, biosensors, and separation technologies. The fluorine atom in its structure can enhance binding affinity and metabolic stability, making it valuable in the design of bioactive molecules.

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Test Parameter Specification
Appearance solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,630.00
inventory 250mg
10-20 days ฿11,460.00
inventory 1g
10-20 days ฿27,960.00
(4-((2-Acrylamidoethyl)carbamoyl)-3-fluorophenyl)boronic acid
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its boronic acid functional group, which is known for its ability to form stable covalent bonds with diols and other nucleophiles. It is often employed in the development of boron-containing drugs, particularly in the synthesis of protease inhibitors and other therapeutic agents targeting specific enzymes. Additionally, its acrylamide moiety makes it suitable for polymerization reactions, enabling its use in the creation of advanced materials such as hydrogels or molecularly imprinted polymers. These materials have applications in drug delivery systems, biosensors, and separation technologies. The fluorine atom in its structure can enhance binding affinity and metabolic stability, making it valuable in the design of bioactive molecules.
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