(4-(9H-Carbazol-9-yl)phenyl)boronic acid
98%
Reagent
Code: #90477
CAS Number
419536-33-7
blur_circular Chemical Specifications
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Molecular Information
Weight
287.13 g/mol
Formula
C₁₈H₁₄BNO₂
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Registry Numbers
MDL Number
MFCD13176534
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Physical Properties
Boiling Point
452.7°C
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Storage & Handling
Density
1.2g/mL
Storage
room temperature, dry
description Product Description
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, which is widely employed to form carbon-carbon bonds. Its boronic acid group makes it a valuable building block for creating complex organic molecules, especially in the pharmaceutical industry for drug development. Additionally, it is utilized in materials science for the synthesis of organic electronic materials, such as OLEDs (organic light-emitting diodes), due to its carbazole moiety, which imparts desirable electronic properties. Its applications also extend to the development of sensors and advanced polymers.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Off-white powder |
Purity | 97.5-100 |
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(4-(9H-Carbazol-9-yl)phenyl)boronic acid
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, which is widely employed to form carbon-carbon bonds. Its boronic acid group makes it a valuable building block for creating complex organic molecules, especially in the pharmaceutical industry for drug development. Additionally, it is utilized in materials science for the synthesis of organic electronic materials, such as OLEDs (organic light-emitting diodes), due to its carbazole moiety, which imparts desirable electronic properties. Its applications also extend to the development of sensors and advanced polymers.
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