(4-Hydroxy-3-nitrophenyl)boronic acid

98%

Reagent Code: #90713
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CAS Number 850568-75-1

science Other reagents with same CAS 850568-75-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.93 g/mol
Formula C₆H₆BNO₅
thermostat Physical Properties
Melting Point 111-113°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various bioactive molecules, particularly in the development of enzyme inhibitors and receptor modulators. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to construct complex organic frameworks. Additionally, it is employed in the design of sensors and probes for detecting biological molecules, owing to its ability to form reversible complexes with diols and other functional groups. Its nitro and hydroxyl groups further enhance its reactivity, making it a versatile building block in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,422.00
inventory 250mg
10-20 days ฿4,113.00

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(4-Hydroxy-3-nitrophenyl)boronic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various bioactive molecules, particularly in the development of enzyme inhibitors and receptor modulators. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to construct complex organic frameworks. Additionally, it is employed in the design of sensors and probes for detecting biological molecules, owing to its

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various bioactive molecules, particularly in the development of enzyme inhibitors and receptor modulators. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to construct complex organic frameworks. Additionally, it is employed in the design of sensors and probes for detecting biological molecules, owing to its ability to form reversible complexes with diols and other functional groups. Its nitro and hydroxyl groups further enhance its reactivity, making it a versatile building block in medicinal chemistry and material science.

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