3-(2-Bromoacetamido)phenylboronic acid, pinacol ester
95%
Reagent
Code: #83506
CAS Number
2096331-74-5
blur_circular Chemical Specifications
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Molecular Information
Weight
340.02 g/mol
Formula
C₁₄H₁₉BBrNO₃
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Registry Numbers
MDL Number
MFCD18783180
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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.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Light Yellow powder |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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