(4-(Propylcarbamoyl)phenyl)boronic acid

98%

Reagent Code: #227845
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CAS Number 171922-46-6

science Other reagents with same CAS 171922-46-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.03 g/mol
Formula C₁₀H₁₄BNO₃
badge Registry Numbers
MDL Number MFCD06656015
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of proteasome inhibitors like bortezomib, which is employed in cancer therapy. Its boronic acid functional group enables reversible interactions with biological targets containing diols or active serine residues, making it valuable in medicinal chemistry for enzyme inhibition. Also utilized in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks in drug discovery and in the design of sensors for sugar detection due to its affinity for diol-containing molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿850.00
inventory 250mg
10-20 days ฿1,380.00
inventory 1g
10-20 days ฿4,010.00

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(4-(Propylcarbamoyl)phenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of proteasome inhibitors like bortezomib, which is employed in cancer therapy. Its boronic acid functional group enables reversible interactions with biological targets containing diols or active serine residues, making it valuable in medicinal chemistry for enzyme inhibition. Also utilized in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks in drug discovery and in the design of senso

Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of proteasome inhibitors like bortezomib, which is employed in cancer therapy. Its boronic acid functional group enables reversible interactions with biological targets containing diols or active serine residues, making it valuable in medicinal chemistry for enzyme inhibition. Also utilized in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks in drug discovery and in the design of sensors for sugar detection due to its affinity for diol-containing molecules.

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