4-(aminomethyl)phenylboronic acid
≥95%
Reagent
Code: #90478
CAS Number
51239-46-4
blur_circular Chemical Specifications
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Molecular Information
Weight
150.97 g/mol
Formula
C₇H₁₀BNO₂
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Registry Numbers
MDL Number
MFCD06213214
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Storage & Handling
Storage
2~8℃
description Product Description
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds in pharmaceuticals and organic materials. It serves as a boronic acid derivative in the development of sensors for detecting sugars and other diols due to its affinity for cis-diols. Applied in the preparation of bioactive molecules and drug candidates, particularly in cancer research and enzyme inhibition studies. Also utilized in the modification of polymers and surfaces for biomedical applications, such as targeted drug delivery systems. Its amino group allows for further functionalization, making it valuable in bioconjugation and the creation of peptide-based therapeutics.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | solid |
Purity | 94.5-100 |
Infrared Spectrum | Conforms to Structure |
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4-(aminomethyl)phenylboronic acid
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds in pharmaceuticals and organic materials. It serves as a boronic acid derivative in the development of sensors for detecting sugars and other diols due to its affinity for cis-diols. Applied in the preparation of bioactive molecules and drug candidates, particularly in cancer research and enzyme inhibition studies. Also utilized in the modification of polymers and surfaces for biomedical applications, such as targeted drug delivery systems. Its amino group allows for further functionalization, making it valuable in bioconjugation and the creation of peptide-based therapeutics.
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