(9H-Carbazol-3-yl)boronic acid
≥95%
Reagent
Code: #37144
CAS Number
851524-97-5
science Other reagents with same CAS 851524-97-5
blur_circular Chemical Specifications
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Molecular Information
Weight
211.02 g/mol
Formula
C₁₂H₁₀BNO₂
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Registry Numbers
MDL Number
MFCD04113810
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Physical Properties
Boiling Point
509.2±42.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
(9H-Carbazol-3-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The compound serves as a key intermediate in the preparation of carbazole derivatives, which are known for their applications in optoelectronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Additionally, it is utilized in the development of bioactive compounds and polymers with specific functional properties. Its boronic acid group facilitates efficient and selective coupling reactions, enhancing its utility in diverse chemical transformations.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Report Result |
| Purity (%) | 95-100% |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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