4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
97%
Reagent
Code: #241246
CAS Number
1255309-13-7
blur_circular Chemical Specifications
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Molecular Information
Weight
293.17 g/mol
Formula
C₁₈H₂₀BNO₂
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Registry Numbers
MDL Number
MFCD16996079
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Storage & Handling
Storage
Room temperature
description Product Description
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing conjugated organic materials. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of organic semiconductors, OLEDs (organic light-emitting diodes), and pharmaceutical intermediates. The carbazole moiety contributes hole-transport properties and thermal stability, which are advantageous in optoelectronic devices. It is also employed in the synthesis of functional polymers and small molecules for use in photovoltaics and sensors.
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