3-(N,N-Dimethylamino)phenylboronic acid

95%

Reagent Code: #117474
label
Alias 3-(N,N-Dimethylamino)phenylboronic acid; 3-(N,N-Dimethylamino)phenylboronic acid (in the form of its hydrochloride salt);
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CAS Number 178752-79-9

science Other reagents with same CAS 178752-79-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.00 g/mol
Formula C₈H₁₂BNO₂
badge Registry Numbers
MDL Number MFCD01318996
thermostat Physical Properties
Melting Point 178-190ºC
Boiling Point 344ºC
inventory_2 Storage & Handling
Density 1.12 g/cm3
Storage 2~8°C, dry, inert gas protection

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds, which are important in pharmaceuticals and organic materials. It serves as a boronic acid derivative in the preparation of complex organic molecules, particularly in drug discovery and development. Its role in forming carbon-carbon bonds makes it valuable in creating biologically active compounds and advanced materials. Additionally, it is utilized in the development of sensors and probes for detecting specific analytes due to its ability to interact with diols and other functional groups.

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Test Parameter Specification
Purity (Titration by NaOH) 94.5-100
Appearance White to off-white to tan to grey to purple powder, crystals, crystalline powder and/or chunks
Proton NMR Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,580.00
inventory 200mg
10-20 days ฿420.00
inventory 1g
10-20 days ฿900.00

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3-(N,N-Dimethylamino)phenylboronic acid
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds, which are important in pharmaceuticals and organic materials. It serves as a boronic acid derivative in the preparation of complex organic molecules, particularly in drug discovery and development. Its role in forming carbon-carbon bonds makes it valuable in creating biologically active compounds and advanced materials. Additionally, it is utilized in the development of sensors and probes for det

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds, which are important in pharmaceuticals and organic materials. It serves as a boronic acid derivative in the preparation of complex organic molecules, particularly in drug discovery and development. Its role in forming carbon-carbon bonds makes it valuable in creating biologically active compounds and advanced materials. Additionally, it is utilized in the development of sensors and probes for detecting specific analytes due to its ability to interact with diols and other functional groups.

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