4-Aminocarbonylphenylboronic acid
98%
Reagent
Code: #90618
Alias
4-carbamoylphenylboronic acid
CAS Number
123088-59-5
blur_circular Chemical Specifications
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Molecular Information
Weight
164.95 g/mol
Formula
H₂NCOC₆H₄BOH₂
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Registry Numbers
MDL Number
MFCD03411940
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Physical Properties
Melting Point
242-252°C
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Storage & Handling
Storage
2~8°C
description Product Description
Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of enzyme inhibitors and receptor modulators. It plays a significant role in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create complex organic molecules. Additionally, it is utilized in the preparation of boronic acid derivatives for sensing applications, such as glucose detection in medical diagnostics. Its ability to form stable complexes with diols and other molecules makes it valuable in the design of molecular probes and sensors for biochemical research.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Melting Point | 230-240 |
Purity (HPLC) | 98-100 |
Purity (Titration with NaOH) | 97.5-102.5 |
Appearance | White to tan crystal to powder |
Infrared Spectrometry | Conforms to Structure |
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4-Aminocarbonylphenylboronic acid
Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of enzyme inhibitors and receptor modulators. It plays a significant role in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create complex organic molecules. Additionally, it is utilized in the preparation of boronic acid derivatives for sensing applications, such as glucose detection in medical diagnostics. Its ability to form stable complexes with diols and other molecules makes it valuable in the design of molecular probes and sensors for biochemical research.
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