(4-(((Benzyloxy)carbonyl)amino)-2-fluorophenyl)boronic acid

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Reagent Code: #89176
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CAS Number 874290-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.07 g/mol
Formula C₁₄H₁₃BFNO₄
badge Registry Numbers
MDL Number MFCD20040311
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its fluorophenyl group enhances reactivity and selectivity in these reactions, making it valuable in pharmaceutical research for developing drug candidates. Additionally, the benzyloxycarbonyl (Cbz) protecting group ensures stability during synthesis, allowing for selective deprotection when needed. This compound is also explored in materials science for creating advanced polymers and functional materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days $50.44
inventory 5g
10-20 days $176.15
inventory 25g
10-20 days $615.75
(4-(((Benzyloxy)carbonyl)amino)-2-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its fluorophenyl group enhances reactivity and selectivity in these reactions, making it valuable in pharmaceutical research for developing drug candidates. Additionally, the benzyloxycarbonyl (Cbz) protecting group ensures stability during synthesis, allowing for selective deprotection when needed. This compound is also explored in materials science for creating advanced polymers and functional materials.
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