9-([1,1'-Biphenyl]-4-yl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole丨CAS 1427213-44-2

9-([1,1'-Biphenyl]-4-yl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole丨CAS 1427213-44-2
Product Introduction:
Catalog No.: SS120461
CAS No.: 1427213-44-2
Purity(HPLC): 99% min
Product Name: 9-([1,1'-Biphenyl]-4-yl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
Molecular Formula: C30H28BNO2
Molecular Weight: 445.35982
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 9-([1,1'-biphenyl]-4-yl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9h-carbazole丨cas 1427213-44-2 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance: White powder
Purity (HPLC): 99% min
Melting Point (MP): 255~259℃

 

 

 

Applications

 

1. OLED Materials (Organic Light-Emitting Diodes)

Serves as a building block for the synthesis of high-efficiency blue or deep-blue emitters.

Carbazole units provide high triplet energy, thermal stability, and excellent hole-transporting properties.

The biphenyl unit enhances π-conjugation, improving charge mobility and electroluminescence.

2. Photovoltaics and Organic Semiconductors

Incorporated into donor–acceptor architectures for organic solar cells and field-effect transistors.

Conjugated structure supports photo-induced electron transfer.

3. Suzuki–Miyaura Coupling Reactions

The pinacol boronic ester group allows palladium-catalyzed cross-coupling, facilitating the creation of custom-designed organic molecules.

Used to attach additional aryl or heteroaryl groups, making it a versatile intermediate for research and development.

4. Material Science and Molecular Design

Acts as a precursor for tunable organic fluorophores, nonlinear optical materials, and sensors.

Ideal for designing compounds with tailored photophysical properties due to its structural rigidity and extended conjugation.

 

Benefits

 

✅ High Electronic Performance

Combines electron-donating carbazole with extended conjugated systems, boosting charge mobility and light emission.

✅ Synthetic Flexibility

The boronate ester functionality enables diverse molecular architectures through cross-coupling chemistry.

✅ Thermal and Photostability

Suitable for use in high-temperature vacuum deposition processes for OLED fabrication.

✅ Enhanced Luminescence

Excellent potential for generating high quantum yield fluorescent materials, especially in blue-light emission.

✅ Customizable Molecular Scaffold

Widely used in materials chemistry for structural modification and optimization of device performance.

 

Conclusion

 

9-([1,1'-Biphenyl]-4-yl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole (CAS 1427213-44-2) is a high-value compound in the field of organic electronics. Its robust structure, functional boronic ester, and electronically active carbazole-biphenyl core make it ideal for OLEDs, OPVs, and other electro-optic devices. As demand grows for advanced organic materials, this compound serves as a key intermediate for next-generation molecular design.

 

 

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