3-(N,O-Dimethylhydroxylaminocarbonyl)phenylboronic acid

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Reagent Code: #90003
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CAS Number 723281-57-0

science Other reagents with same CAS 723281-57-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.01 g/mol
Formula C₉H₁₂BNO₄
badge Registry Numbers
MDL Number MFCD04115699
thermostat Physical Properties
Melting Point 66-70°C
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. It is particularly valuable in pharmaceutical research for constructing biaryl compounds, which are common in drug development. Additionally, it serves as a boronic acid derivative in sensor applications, aiding in the detection of sugars and other analytes. Its stability and reactivity make it a versatile tool in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,420.00
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3-(N,O-Dimethylhydroxylaminocarbonyl)phenylboronic acid
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Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. It is particularly valuable in pharmaceutical research for constructing biaryl compounds, which are common in drug development. Additionally, it serves as a boronic acid derivative in sensor applications, aiding in the detection of sugars and other analytes. Its stability and reactivity make it a versatile tool in medicinal chemistry and material scie

Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. It is particularly valuable in pharmaceutical research for constructing biaryl compounds, which are common in drug development. Additionally, it serves as a boronic acid derivative in sensor applications, aiding in the detection of sugars and other analytes. Its stability and reactivity make it a versatile tool in medicinal chemistry and material science.

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