3-(2-Bromoacetamido)phenylboronic acid, pinacol ester

95%

Reagent Code: #83506
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CAS Number 2096331-74-5

science Other reagents with same CAS 2096331-74-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 340.02 g/mol
Formula C₁₄H₁₉BBrNO₃
badge Registry Numbers
MDL Number MFCD18783180
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, its bromoacetamido moiety allows for further functionalization, making it a versatile building block in medicinal chemistry for designing biologically active compounds.

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Test Parameter Specification
Appearance Light Yellow powder
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,589.00
inventory 1g
10-20 days ฿14,436.00

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3-(2-Bromoacetamido)phenylboronic acid, pinacol ester
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, its bromoacetamido moiety allows for furt

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, its bromoacetamido moiety allows for further functionalization, making it a versatile building block in medicinal chemistry for designing biologically active compounds.

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