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Product Line: Electronic Chemicals

(9-phenyl-9H-carbazol-4-yl)boronic acid

CAS 1370555-65-9

Molecular structure of (9-phenyl-9H-carbazol-4-yl)boronic acid

CAS · 1370555-65-9

01

Product Overview

(9-phenyl-9H-carbazol-4-yl)boronic acid is a high-purity oled-materials supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance Off-white to white powder
Purity (HPLC) 99.5% min
03

Applications

 

1. Building Block for Organic Synthesis

Used extensively as a key intermediate in Suzuki-Miyaura cross-coupling reactions to form C-C bonds.

Enables the synthesis of complex carbazole derivatives and conjugated organic molecules.

2. Organic Electronics and Photonics

Integral in the preparation of organic semiconductors, OLED materials, and photovoltaic components.

Carbazole-based compounds are valued for their electroluminescent properties, charge transport ability, and thermal stability.

Boronic acid group facilitates polymerization and functionalization, allowing tailored electronic properties.

3. Material Science Research

Used in the design and synthesis of functional polymers and molecular materials with applications in sensors, displays, and light-emitting devices.

4. Pharmaceutical Chemistry

Carbazole derivatives have biological activity; this compound can serve as a precursor for drug development and bioactive molecule synthesis.

04

Benefits

✅ Versatile Reactivity

Boronic acid group enables efficient coupling reactions under mild conditions.

✅ Stable Carbazole Core

Provides robust aromatic framework with excellent photophysical properties.

✅ Facilitates Advanced Material Design

Supports the creation of customized organic electronic materials.

✅ Widely Used in Research

Popular intermediate for both academic and industrial laboratories.

05

Conclusion

(9-Phenyl-9H-carbazol-4-yl)boronic acid (CAS 1370555-65-9) is an important organoboron compound serving as a versatile building block in organic synthesis, particularly in cross-coupling reactions. Its combination of a boronic acid functional group with a photophysically active carbazole core makes it valuable for developing advanced materials in organic electronics, photonics, and pharmaceuticals. The compound's stability and reactivity continue to facilitate innovations in material science and synthetic chemistry.

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