3-Ethoxycarbonylphenylboronic acid
97%
Reagent
Code: #90117
Alias
3-Ethoxycarbonylphenylboronic acid
CAS Number
4334-87-6
blur_circular Chemical Specifications
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Molecular Information
Weight
193.99 g/mol
Formula
C₉H₁₁BO₄
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Registry Numbers
MDL Number
MFCD02179444
thermostat
Physical Properties
Melting Point
131-136 °C
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Storage & Handling
Storage
2~8°C
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds widely applied in pharmaceuticals and organic materials. It serves as a boronic acid derivative in the production of complex organic molecules, particularly in drug development for targeting specific biological pathways. Its role in creating carbon-carbon bonds makes it valuable in agrochemical research for developing new pesticides and herbicides. Additionally, it is utilized in material science for designing advanced polymers and organic electronics. Its stability and reactivity make it a preferred choice in fine chemical synthesis and industrial applications.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Melting point | 135-139 |
Purity (HPLC) | 97-100% |
Appearance | White to off-white powder |
Infrared Spectrometry | Conforms to Structure |
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3-Ethoxycarbonylphenylboronic acid
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds widely applied in pharmaceuticals and organic materials. It serves as a boronic acid derivative in the production of complex organic molecules, particularly in drug development for targeting specific biological pathways. Its role in creating carbon-carbon bonds makes it valuable in agrochemical research for developing new pesticides and herbicides. Additionally, it is utilized in material science for designing advanced polymers and organic electronics. Its stability and reactivity make it a preferred choice in fine chemical synthesis and industrial applications.
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