3,5-Bis(imidazol-1-yl)phenylboronic acid

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Reagent Code: #89922
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CAS Number 2225180-01-6

science Other reagents with same CAS 2225180-01-6

blur_circular Chemical Specifications

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Weight 254.05234 g/mol
Formula C₁₂H₁₁BN₄O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This arylboronic acid derivative is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds between aryl groups. It also serves as a key building block in materials science for supramolecular structures, coordination polymers, and metal-organic frameworks (MOFs). The boronic acid functionality enables reversible covalent interactions, ideal for dynamic and responsive materials. Furthermore, it is applied in sensor design for detecting sugars and diol-containing molecules through stable cyclic ester formation. In medicinal chemistry, it shows potential in drug delivery systems, utilizing its affinity for biological targets.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,080.00
inventory 25mg
10-20 days ฿29,304.00

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3,5-Bis(imidazol-1-yl)phenylboronic acid
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This arylboronic acid derivative is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds between aryl groups. It also serves as a key building block in materials science for supramolecular structures, coordination polymers, and metal-organic frameworks (MOFs). The boronic acid functionality enables reversible covalent interactions, ideal for dynamic and responsive materials. Furthermore, it is applied in sensor design for detecting sugars a

This arylboronic acid derivative is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds between aryl groups. It also serves as a key building block in materials science for supramolecular structures, coordination polymers, and metal-organic frameworks (MOFs). The boronic acid functionality enables reversible covalent interactions, ideal for dynamic and responsive materials. Furthermore, it is applied in sensor design for detecting sugars and diol-containing molecules through stable cyclic ester formation. In medicinal chemistry, it shows potential in drug delivery systems, utilizing its affinity for biological targets.

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