4,4,5,5-Tetramethyl-2-(4-phenylnaphthalen-1-yl)-1,3,2-dioxaborolane
97%
Reagent
Code: #244103
CAS Number
1422181-38-1
blur_circular Chemical Specifications
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Molecular Information
Weight
330.23 g/mol
Formula
C₂₂H₂₃BO₂
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Registry Numbers
MDL Number
MFCD32670138
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Storage & Handling
Storage
Room temperature, seal, dry
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, particularly in pharmaceuticals and advanced materials. Its arylboronate ester structure provides high stability and reactivity under palladium catalysis, making it valuable in the preparation of conjugated systems such as organic semiconductors and fluorescent dyes. Commonly employed in research settings for the development of OLEDs and other optoelectronic devices due to its ability to incorporate naphthalene-based aromatic units into larger π-conjugated frameworks.
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